{"id":99,"date":"2025-01-15T15:31:43","date_gmt":"2025-01-15T15:31:43","guid":{"rendered":"http:\/\/localhost\/genecontrol\/?post_type=content&#038;p=99"},"modified":"2025-02-12T08:26:49","modified_gmt":"2025-02-12T08:26:49","slug":"chapter-14-gene-regulation-and-human-disease","status":"publish","type":"content","link":"https:\/\/staging.routledgelearning.com\/genecontrol\/student-resources\/chapter-14-gene-regulation-and-human-disease\/","title":{"rendered":"Chapter 14: Gene Regulation and Human Disease"},"content":{"rendered":"\n<p>The central role of gene control processes in normal cellular function which has been discussed throughout this book makes it inevitable that abnormalities in such processes will result in disease. In addition to the abnormalities that occur in cancer (see Chapter 13), it has been demonstrated that many human genetic diseases involve the inheritance of mutated genes encoding proteins that regulate gene expression. A number of different diseases have been shown to involve mutations in proteins involved in each of the three fundamental processes that regulate gene expression (see Chapters 4\u20139), namely the processes of transcription itself, the regulation of chromatin structure which is necessary for transcription to occur, and post-transcriptional processes. These cases will be discussed in Sections 14.1\u201314.3 of this chapter, respectively. Section 14.4 will describe the manner in which abnormalities in regulatory RNAs are involved in human genetic diseases and Section 14.5 will describe alterations in gene regulatory processes that can occur in human infectious disease. Finally, it is clear that the insights obtained by studies on gene regulation in cancer and other human diseases may lead to the development of effective therapies for manipulating gene expression in these diseases and this is discussed in Section 14.6.<\/p>\n\n\n\n<div class=\"wp-block-group alignwide is-layout-flow wp-block-group-is-layout-flow\">\n<hr class=\"wp-block-separator alignwide has-alpha-channel-opacity\"\/>\n<\/div>\n\n\n\n<div class=\"wp-block-columns is-layout-flex wp-container-core-columns-is-layout-28f84493 wp-block-columns-is-layout-flex\">\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\" style=\"flex-basis:70%\">\n<h2 class=\"wp-block-heading\" id=\"aioseo-multiple-choice-questions\" style=\"padding-top:0;padding-right:0;padding-bottom:0;padding-left:0\">Multiple-choice questions<\/h2>\n\n\n<script>\n                            if (window.qmn_quiz_data === undefined) {\n                                    window.qmn_quiz_data = new Object();\n                            }\n                    <\/script><script>window.qmn_quiz_data[\"14\"] = {\"quiz_id\":\"14\",\"quiz_name\":\"chapter14\",\"disable_answer\":0,\"ajax_show_correct\":0,\"progress_bar\":\"0\",\"contact_info_location\":0,\"qpages\":{\"1\":{\"id\":\"1\",\"quizID\":\"14\",\"pagekey\":\"DKJZEuIy\",\"hide_prevbtn\":\"0\"}},\"skip_validation_time_expire\":0,\"timer_limit_val\":0,\"disable_scroll_next_previous_click\":0,\"disable_scroll_on_result\":0,\"disable_first_page\":0,\"enable_result_after_timer_end\":0,\"enable_quick_result_mc\":0,\"end_quiz_if_wrong\":0,\"form_disable_autofill\":0,\"disable_mathjax\":0,\"enable_quick_correct_answer_info\":\"0\",\"quick_result_correct_answer_text\":\"Correct! You have selected correct answer.\",\"quick_result_wrong_answer_text\":\"Wrong! You have selected wrong answer.\",\"quiz_processing_message\":\"\",\"quiz_limit_choice\":\"Limit of choice is reached.\",\"not_allow_after_expired_time\":0,\"scheduled_time_end\":false,\"prevent_reload\":0,\"limit_email_based_submission\":0,\"total_user_tries\":0,\"is_logged_in\":false,\"pagination\":{\"amount\":1,\"section_comments\":\"\",\"total_questions\":10,\"previous_text\":\"Previous\",\"next_text\":\"Next\",\"start_quiz_survey_text\":\"Start Quiz\",\"submit_quiz_text\":\"Submit\"},\"error_messages\":{\"email_error_text\":\"Not a valid e-mail address!\",\"number_error_text\":\"This field must be a number!\",\"incorrect_error_text\":\"The entered text is not correct!\",\"empty_error_text\":\"Please complete all required fields!\",\"contact_field_required_error_text\":\"Please complete all required fields!\",\"url_error_text\":\"The entered URL is not valid!\",\"minlength_error_text\":\"Required atleast %minlength% characters.\",\"maxlength_error_text\":\"Maximum %maxlength% 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mutation?\",\"answer_array\":\"a:4:{i:0;a:5:{i:0;s:170:\\\"The Pax6 mutation leads to an enhanced production of the mutant protein, which exerts a dominant negative effect on the wild-type protein, inhibiting its normal function.\\\";i:1;s:0:\\\"\\\";i:2;s:0:\\\"\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:1;a:5:{i:0;s:205:\\\"The dominant nature of the Pax6 mutation is attributed to the formation of heterodimers between the mutant and wild-type proteins, leading to an increased stability and enhanced activation of target genes.\\\";i:1;s:0:\\\"\\\";i:2;s:0:\\\"\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:2;a:5:{i:0;s:196:\\\" Haploid insufficiency is the underlying cause of the Pax6 mutation's dominance, as a single functional copy of the gene cannot produce sufficient protein to effectively activate its target genes.\\\";i:1;s:0:\\\"\\\";i:2;s:1:\\\"1\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:3;a:5:{i:0;s:157:\\\"The Pax6 mutation triggers a 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2\\\";s:8:\\\"required\\\";i:0;s:12:\\\"answerEditor\\\";s:4:\\\"text\\\";s:15:\\\"featureImageSrc\\\";s:0:\\\"\\\";s:11:\\\"matchAnswer\\\";s:6:\\\"random\\\";s:14:\\\"case_sensitive\\\";s:0:\\\"\\\";s:14:\\\"answer_columns\\\";s:0:\\\"\\\";s:16:\\\"image_size-width\\\";s:0:\\\"\\\";s:17:\\\"image_size-height\\\";s:0:\\\"\\\";s:8:\\\"autofill\\\";s:0:\\\"\\\";s:23:\\\"limit_multiple_response\\\";s:0:\\\"\\\";s:17:\\\"file_upload_limit\\\";s:0:\\\"\\\";s:16:\\\"file_upload_type\\\";s:0:\\\"\\\";}\",\"category\":\"\",\"linked_question\":\"\",\"deleted\":\"0\",\"deleted_question_bank\":\"0\",\"answers\":[{\"0\":\"The Pax6 mutation leads to an enhanced production of the mutant protein, which exerts a dominant negative effect on the wild-type protein, inhibiting its normal function.\",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"},{\"0\":\"The dominant nature of the Pax6 mutation is attributed to the formation of heterodimers between the mutant and wild-type proteins, leading to an increased stability and enhanced activation of target genes.\",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"},{\"0\":\" Haploid insufficiency is the underlying cause of the Pax6 mutation's dominance, as a single functional copy of the gene cannot produce sufficient protein to effectively activate its target genes.\",\"1\":\"\",\"2\":\"1\",\"3\":\"\",\"label\":\"\"},{\"0\":\"The Pax6 mutation triggers a gain-of-function effect, causing the mutant protein to be hyperactive and override the normal function of the wild-type protein.\",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"}]},\"157\":{\"question_id\":\"157\",\"quiz_id\":\"14\",\"question_name\":\"Mutations within an enhancer located 25 kb upstream of the PTF1A gene leads to\\u2026?\",\"answer_array\":\"a:4:{i:0;a:5:{i:0;s:113:\\\"disruption of transcription factor binding, resulting in reduced PTF1A gene expression and pancreatic hypoplasia.\\\";i:1;s:0:\\\"\\\";i:2;s:1:\\\"1\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:1;a:5:{i:0;s:97:\\\"hyperactivation of the PTF1A gene, resulting in excessive pancreatic development and hypertrophy.\\\";i:1;s:0:\\\"\\\";i:2;s:0:\\\"\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:2;a:5:{i:0;s:116:\\\"suppression of the PTF1A gene, leading to impaired pancreatic exocrine function and exocrine pancreas insufficiency.\\\";i:1;s:0:\\\"\\\";i:2;s:0:\\\"\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:3;a:5:{i:0;s:136:\\\"alternative splicing of the PTF1A gene, leading to the formation of a non-functional protein and the development of pancreatic 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3\\\";s:8:\\\"required\\\";i:0;s:12:\\\"answerEditor\\\";s:4:\\\"text\\\";s:15:\\\"featureImageSrc\\\";s:0:\\\"\\\";s:11:\\\"matchAnswer\\\";s:6:\\\"random\\\";s:14:\\\"case_sensitive\\\";s:0:\\\"\\\";s:14:\\\"answer_columns\\\";s:0:\\\"\\\";s:16:\\\"image_size-width\\\";s:0:\\\"\\\";s:17:\\\"image_size-height\\\";s:0:\\\"\\\";s:8:\\\"autofill\\\";s:0:\\\"\\\";s:23:\\\"limit_multiple_response\\\";s:0:\\\"\\\";s:17:\\\"file_upload_limit\\\";s:0:\\\"\\\";s:16:\\\"file_upload_type\\\";s:0:\\\"\\\";}\",\"category\":\"\",\"linked_question\":\"\",\"deleted\":\"0\",\"deleted_question_bank\":\"0\",\"answers\":[{\"0\":\"disruption of transcription factor binding, resulting in reduced PTF1A gene expression and pancreatic hypoplasia.\",\"1\":\"\",\"2\":\"1\",\"3\":\"\",\"label\":\"\"},{\"0\":\"hyperactivation of the PTF1A gene, resulting in excessive pancreatic development and hypertrophy.\",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"},{\"0\":\"suppression of the PTF1A gene, leading to impaired pancreatic exocrine function and exocrine pancreas insufficiency.\",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"},{\"0\":\"alternative splicing of the PTF1A gene, leading to the formation of a non-functional protein and the development of pancreatic agenesis.\",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"}]},\"158\":{\"question_id\":\"158\",\"quiz_id\":\"14\",\"question_name\":\"What is the consequence of having a single inactive CBP gene?\",\"answer_array\":\"a:4:{i:0;a:5:{i:0;s:87:\\\"Abnormal embryonic development and organogenesis, leading to early embryonic lethality.\\\";i:1;s:0:\\\"\\\";i:2;s:0:\\\"\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:1;a:5:{i:0;s:111:\\\"Impaired chromatin remodeling and DNA repair mechanisms, causing widespread genomic instability and cell death.\\\";i:1;s:0:\\\"\\\";i:2;s:0:\\\"\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:2;a:5:{i:0;s:54:\\\"Uncontrolled cell proliferation and tumor development.\\\";i:1;s:0:\\\"\\\";i:2;s:0:\\\"\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:3;a:5:{i:0;s:132:\\\"Rubinstein-Taybi syndrome characterized by mental and physical abnormalities due to impaired neural development and gene regulation.\\\";i:1;s:0:\\\"\\\";i:2;s:1:\\\"1\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}}\",\"answer_one\":\"\",\"answer_one_points\":\"0\",\"answer_two\":\"\",\"answer_two_points\":\"0\",\"answer_three\":\"\",\"answer_three_points\":\"0\",\"answer_four\":\"\",\"answer_four_points\":\"0\",\"answer_five\":\"\",\"answer_five_points\":\"0\",\"answer_six\":\"\",\"answer_six_points\":\"0\",\"correct_answer\":\"0\",\"question_answer_info\":\"\",\"comments\":\"1\",\"hints\":\"\",\"question_order\":\"0\",\"question_type\":\"0\",\"question_type_new\":\"0\",\"question_settings\":\"a:13:{s:14:\\\"question_title\\\";s:10:\\\"Question 4\\\";s:8:\\\"required\\\";i:0;s:12:\\\"answerEditor\\\";s:4:\\\"text\\\";s:15:\\\"featureImageSrc\\\";s:0:\\\"\\\";s:11:\\\"matchAnswer\\\";s:6:\\\"random\\\";s:14:\\\"case_sensitive\\\";s:0:\\\"\\\";s:14:\\\"answer_columns\\\";s:0:\\\"\\\";s:16:\\\"image_size-width\\\";s:0:\\\"\\\";s:17:\\\"image_size-height\\\";s:0:\\\"\\\";s:8:\\\"autofill\\\";s:0:\\\"\\\";s:23:\\\"limit_multiple_response\\\";s:0:\\\"\\\";s:17:\\\"file_upload_limit\\\";s:0:\\\"\\\";s:16:\\\"file_upload_type\\\";s:0:\\\"\\\";}\",\"category\":\"\",\"linked_question\":\"\",\"deleted\":\"0\",\"deleted_question_bank\":\"0\",\"answers\":[{\"0\":\"Abnormal embryonic development and organogenesis, leading to early embryonic lethality.\",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"},{\"0\":\"Impaired chromatin remodeling and DNA repair mechanisms, causing widespread genomic instability and cell death.\",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"},{\"0\":\"Uncontrolled cell proliferation and tumor development.\",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"},{\"0\":\"Rubinstein-Taybi syndrome characterized by mental and physical abnormalities due to impaired neural development and gene regulation.\",\"1\":\"\",\"2\":\"1\",\"3\":\"\",\"label\":\"\"}]},\"159\":{\"question_id\":\"159\",\"quiz_id\":\"14\",\"question_name\":\"How does the presence of mutant Huntingtin lead to disease development in Huntington\\\\'s disease?\",\"answer_array\":\"a:4:{i:0;a:5:{i:0;s:145:\\\"It forms toxic aggregates that impair cellular trafficking and disrupt organelle function, leading to neuronal dysfunction and neurodegeneration.\\\";i:1;s:0:\\\"\\\";i:2;s:1:\\\"1\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:1;a:5:{i:0;s:121:\\\"It enhances the activity of proteasomes, leading to excessive degradation of essential proteins and cellular dysfunction.\\\";i:1;s:0:\\\"\\\";i:2;s:0:\\\"\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:2;a:5:{i:0;s:112:\\\"It directly binds to DNA promoter regions, causing aberrant gene activation and uncontrolled cell proliferation.\\\";i:1;s:0:\\\"\\\";i:2;s:0:\\\"\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:3;a:5:{i:0;s:147:\\\"Mutant Huntingtin stimulates hyperphosphorylation of neurotransmitter receptors, resulting in impaired synaptic transmission and cognitive decline.\\\";i:1;s:0:\\\"\\\";i:2;s:0:\\\"\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}}\",\"answer_one\":\"\",\"answer_one_points\":\"0\",\"answer_two\":\"\",\"answer_two_points\":\"0\",\"answer_three\":\"\",\"answer_three_points\":\"0\",\"answer_four\":\"\",\"answer_four_points\":\"0\",\"answer_five\":\"\",\"answer_five_points\":\"0\",\"answer_six\":\"\",\"answer_six_points\":\"0\",\"correct_answer\":\"0\",\"question_answer_info\":\"\",\"comments\":\"1\",\"hints\":\"\",\"question_order\":\"0\",\"question_type\":\"0\",\"question_type_new\":\"0\",\"question_settings\":\"a:13:{s:14:\\\"question_title\\\";s:10:\\\"Question 5\\\";s:8:\\\"required\\\";i:0;s:12:\\\"answerEditor\\\";s:4:\\\"text\\\";s:15:\\\"featureImageSrc\\\";s:0:\\\"\\\";s:11:\\\"matchAnswer\\\";s:6:\\\"random\\\";s:14:\\\"case_sensitive\\\";s:0:\\\"\\\";s:14:\\\"answer_columns\\\";s:0:\\\"\\\";s:16:\\\"image_size-width\\\";s:0:\\\"\\\";s:17:\\\"image_size-height\\\";s:0:\\\"\\\";s:8:\\\"autofill\\\";s:0:\\\"\\\";s:23:\\\"limit_multiple_response\\\";s:0:\\\"\\\";s:17:\\\"file_upload_limit\\\";s:0:\\\"\\\";s:16:\\\"file_upload_type\\\";s:0:\\\"\\\";}\",\"category\":\"\",\"linked_question\":\"\",\"deleted\":\"0\",\"deleted_question_bank\":\"0\",\"answers\":[{\"0\":\"It forms toxic aggregates that impair cellular trafficking and disrupt organelle function, leading to neuronal dysfunction and neurodegeneration.\",\"1\":\"\",\"2\":\"1\",\"3\":\"\",\"label\":\"\"},{\"0\":\"It enhances the activity of proteasomes, leading to excessive degradation of essential proteins and cellular dysfunction.\",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"},{\"0\":\"It directly binds to DNA promoter regions, causing aberrant gene activation and uncontrolled cell proliferation.\",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"},{\"0\":\"Mutant Huntingtin stimulates hyperphosphorylation of neurotransmitter receptors, resulting in impaired synaptic transmission and cognitive decline.\",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"}]},\"160\":{\"question_id\":\"160\",\"quiz_id\":\"14\",\"question_name\":\"What is the  underlying cause of the rare human ICF syndrome?\",\"answer_array\":\"a:4:{i:0;a:5:{i:0;s:158:\\\"Mutations in the DNA repair genes, specifically those involved in base excision repair, leading to the accumulation of DNA damage and chromosomal instability.\\\";i:1;s:0:\\\"\\\";i:2;s:0:\\\"\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:1;a:5:{i:0;s:154:\\\"Abnormal DNA methylation patterns resulting from mutations in the DNA methyltransferase genes, leading to genomic instability and altered gene expression.\\\";i:1;s:0:\\\"\\\";i:2;s:1:\\\"1\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:2;a:5:{i:0;s:157:\\\"Deletions in the genes encoding structural proteins involved in centromere formation, leading to impaired chromosome segregation and centromeric instability.\\\";i:1;s:0:\\\"\\\";i:2;s:0:\\\"\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:3;a:5:{i:0;s:153:\\\"Deficiencies in the components of the RNA interference (RNAi) pathway, leading to uncontrolled gene expression and dysregulation of immune-related genes.\\\";i:1;s:0:\\\"\\\";i:2;s:0:\\\"\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}}\",\"answer_one\":\"\",\"answer_one_points\":\"0\",\"answer_two\":\"\",\"answer_two_points\":\"0\",\"answer_three\":\"\",\"answer_three_points\":\"0\",\"answer_four\":\"\",\"answer_four_points\":\"0\",\"answer_five\":\"\",\"answer_five_points\":\"0\",\"answer_six\":\"\",\"answer_six_points\":\"0\",\"correct_answer\":\"0\",\"question_answer_info\":\"\",\"comments\":\"1\",\"hints\":\"\",\"question_order\":\"0\",\"question_type\":\"0\",\"question_type_new\":\"0\",\"question_settings\":\"a:13:{s:14:\\\"question_title\\\";s:10:\\\"Question 6\\\";s:8:\\\"required\\\";i:0;s:12:\\\"answerEditor\\\";s:4:\\\"text\\\";s:15:\\\"featureImageSrc\\\";s:0:\\\"\\\";s:11:\\\"matchAnswer\\\";s:6:\\\"random\\\";s:14:\\\"case_sensitive\\\";s:0:\\\"\\\";s:14:\\\"answer_columns\\\";s:0:\\\"\\\";s:16:\\\"image_size-width\\\";s:0:\\\"\\\";s:17:\\\"image_size-height\\\";s:0:\\\"\\\";s:8:\\\"autofill\\\";s:0:\\\"\\\";s:23:\\\"limit_multiple_response\\\";s:0:\\\"\\\";s:17:\\\"file_upload_limit\\\";s:0:\\\"\\\";s:16:\\\"file_upload_type\\\";s:0:\\\"\\\";}\",\"category\":\"\",\"linked_question\":\"\",\"deleted\":\"0\",\"deleted_question_bank\":\"0\",\"answers\":[{\"0\":\"Mutations in the DNA repair genes, specifically those involved in base excision repair, leading to the accumulation of DNA damage and chromosomal instability.\",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"},{\"0\":\"Abnormal DNA methylation patterns resulting from mutations in the DNA methyltransferase genes, leading to genomic instability and altered gene expression.\",\"1\":\"\",\"2\":\"1\",\"3\":\"\",\"label\":\"\"},{\"0\":\"Deletions in the genes encoding structural proteins involved in centromere formation, leading to impaired chromosome segregation and centromeric instability.\",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"},{\"0\":\"Deficiencies in the components of the RNA interference (RNAi) pathway, leading to uncontrolled gene expression and dysregulation of immune-related genes.\",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"}]},\"161\":{\"question_id\":\"161\",\"quiz_id\":\"14\",\"question_name\":\"How does the inactivation of JARID1C interfere with the ability of REST (RE1-silencing transcription factor) to repress gene expression?\",\"answer_array\":\"a:4:{i:0;a:5:{i:0;s:155:\\\"This leads to abnormal DNA methylation at the RE1 binding sites, preventing REST from binding to its target genes and relieving transcriptional repression.\\\";i:1;s:0:\\\"\\\";i:2;s:0:\\\"\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:1;a:5:{i:0;s:175:\\\"JARID1C physically interacts with REST and recruits co-repressor complexes to the promoter regions of target genes, thereby enhancing REST-mediated transcriptional repression.\\\";i:1;s:0:\\\"\\\";i:2;s:0:\\\"\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:2;a:5:{i:0;s:143:\\\"This disrupts the nuclear localization of REST, preventing it from entering the nucleus and executing its transcriptional repression functions.\\\";i:1;s:0:\\\"\\\";i:2;s:0:\\\"\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:3;a:5:{i:0;s:158:\\\"JARID1C acts as a histone demethylase, removing repressive histone marks at the promoter regions of REST target genes, resulting in increased gene expression.\\\";i:1;s:0:\\\"\\\";i:2;s:1:\\\"1\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}}\",\"answer_one\":\"\",\"answer_one_points\":\"0\",\"answer_two\":\"\",\"answer_two_points\":\"0\",\"answer_three\":\"\",\"answer_three_points\":\"0\",\"answer_four\":\"\",\"answer_four_points\":\"0\",\"answer_five\":\"\",\"answer_five_points\":\"0\",\"answer_six\":\"\",\"answer_six_points\":\"0\",\"correct_answer\":\"0\",\"question_answer_info\":\"\",\"comments\":\"1\",\"hints\":\"\",\"question_order\":\"0\",\"question_type\":\"0\",\"question_type_new\":\"0\",\"question_settings\":\"a:13:{s:14:\\\"question_title\\\";s:10:\\\"Question 7\\\";s:8:\\\"required\\\";i:0;s:12:\\\"answerEditor\\\";s:4:\\\"text\\\";s:15:\\\"featureImageSrc\\\";s:0:\\\"\\\";s:11:\\\"matchAnswer\\\";s:6:\\\"random\\\";s:14:\\\"case_sensitive\\\";s:0:\\\"\\\";s:14:\\\"answer_columns\\\";s:0:\\\"\\\";s:16:\\\"image_size-width\\\";s:0:\\\"\\\";s:17:\\\"image_size-height\\\";s:0:\\\"\\\";s:8:\\\"autofill\\\";s:0:\\\"\\\";s:23:\\\"limit_multiple_response\\\";s:0:\\\"\\\";s:17:\\\"file_upload_limit\\\";s:0:\\\"\\\";s:16:\\\"file_upload_type\\\";s:0:\\\"\\\";}\",\"category\":\"\",\"linked_question\":\"\",\"deleted\":\"0\",\"deleted_question_bank\":\"0\",\"answers\":[{\"0\":\"This leads to abnormal DNA methylation at the RE1 binding sites, preventing REST from binding to its target genes and relieving transcriptional repression.\",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"},{\"0\":\"JARID1C physically interacts with REST and recruits co-repressor complexes to the promoter regions of target genes, thereby enhancing REST-mediated transcriptional repression.\",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"},{\"0\":\"This disrupts the nuclear localization of REST, preventing it from entering the nucleus and executing its transcriptional repression functions.\",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"},{\"0\":\"JARID1C acts as a histone demethylase, removing repressive histone marks at the promoter regions of REST target genes, resulting in increased gene expression.\",\"1\":\"\",\"2\":\"1\",\"3\":\"\",\"label\":\"\"}]},\"162\":{\"question_id\":\"162\",\"quiz_id\":\"14\",\"question_name\":\"A mutation in the SNF2 factor, which is a vital component of the chromatin-remodeling SWI\\\/SNF complex, can lead to \\u03b1-thalassemia combined with mental retardation. This observation suggests that SNF2\\\\'s activity is essential for:\",\"answer_array\":\"a:4:{i:0;a:5:{i:0;s:135:\\\"Facilitating DNA replication by promoting the unwinding of the double helix, allowing the DNA polymerase access to the template strand.\\\";i:1;s:0:\\\"\\\";i:2;s:0:\\\"\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:1;a:5:{i:0;s:126:\\\"Recruiting transcription factors to gene promoter regions, enhancing gene expression and promoting transcriptional activation.\\\";i:1;s:0:\\\"\\\";i:2;s:0:\\\"\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:2;a:5:{i:0;s:143:\\\"Opening the chromatin structure of the \\u03b1-globin genes and other genes, allowing transcriptional machinery access and enabling gene expression.\\\";i:1;s:0:\\\"\\\";i:2;s:1:\\\"1\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:3;a:5:{i:0;s:129:\\\"Mediating post-translational modifications of histone proteins, influencing chromatin condensation and regulating gene silencing.\\\";i:1;s:0:\\\"\\\";i:2;s:0:\\\"\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}}\",\"answer_one\":\"\",\"answer_one_points\":\"0\",\"answer_two\":\"\",\"answer_two_points\":\"0\",\"answer_three\":\"\",\"answer_three_points\":\"0\",\"answer_four\":\"\",\"answer_four_points\":\"0\",\"answer_five\":\"\",\"answer_five_points\":\"0\",\"answer_six\":\"\",\"answer_six_points\":\"0\",\"correct_answer\":\"0\",\"question_answer_info\":\"\",\"comments\":\"1\",\"hints\":\"\",\"question_order\":\"0\",\"question_type\":\"0\",\"question_type_new\":\"0\",\"question_settings\":\"a:13:{s:14:\\\"question_title\\\";s:10:\\\"Question 8\\\";s:8:\\\"required\\\";i:0;s:12:\\\"answerEditor\\\";s:4:\\\"text\\\";s:15:\\\"featureImageSrc\\\";s:0:\\\"\\\";s:11:\\\"matchAnswer\\\";s:6:\\\"random\\\";s:14:\\\"case_sensitive\\\";s:0:\\\"\\\";s:14:\\\"answer_columns\\\";s:0:\\\"\\\";s:16:\\\"image_size-width\\\";s:0:\\\"\\\";s:17:\\\"image_size-height\\\";s:0:\\\"\\\";s:8:\\\"autofill\\\";s:0:\\\"\\\";s:23:\\\"limit_multiple_response\\\";s:0:\\\"\\\";s:17:\\\"file_upload_limit\\\";s:0:\\\"\\\";s:16:\\\"file_upload_type\\\";s:0:\\\"\\\";}\",\"category\":\"\",\"linked_question\":\"\",\"deleted\":\"0\",\"deleted_question_bank\":\"0\",\"answers\":[{\"0\":\"Facilitating DNA replication by promoting the unwinding of the double helix, allowing the DNA polymerase access to the template strand.\",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"},{\"0\":\"Recruiting transcription factors to gene promoter regions, enhancing gene expression and promoting transcriptional activation.\",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"},{\"0\":\"Opening the chromatin structure of the \\u03b1-globin genes and other genes, allowing transcriptional machinery access and enabling gene expression.\",\"1\":\"\",\"2\":\"1\",\"3\":\"\",\"label\":\"\"},{\"0\":\"Mediating post-translational modifications of histone proteins, influencing chromatin condensation and regulating gene silencing.\",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"}]},\"163\":{\"question_id\":\"163\",\"quiz_id\":\"14\",\"question_name\":\"How can alterations in specific post-transcriptional stages of gene regulation contribute to the development of human disease?\",\"answer_array\":\"a:4:{i:0;a:5:{i:0;s:187:\\\"Dysfunction in the 5' cap recognition machinery of mRNA leads to enhanced cap-binding, resulting in increased mRNA stability and protein translation, causing hyperproliferative disorders.\\\";i:1;s:0:\\\"\\\";i:2;s:0:\\\"\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:1;a:5:{i:0;s:223:\\\"Abnormalities in RNA-binding proteins that mediate alternative splicing result in improper splice site selection, leading to the production of non-functional protein isoforms and contributing to neurodegenerative disorders.\\\";i:1;s:0:\\\"\\\";i:2;s:1:\\\"1\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:2;a:5:{i:0;s:183:\\\"Disruptions in the polyadenylation signal sequences of pre-mRNA transcripts lead to premature polyadenylation, resulting in truncated mRNA transcripts and subsequent mRNA degradation.\\\";i:1;s:0:\\\"\\\";i:2;s:0:\\\"\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:3;a:5:{i:0;s:210:\\\"Dysregulation of the RNA-induced silencing complex components leads to enhanced microRNA-mediated gene silencing, resulting in the downregulation of critical tumor suppressor genes, contributing to oncogenesis.\\\";i:1;s:0:\\\"\\\";i:2;s:0:\\\"\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}}\",\"answer_one\":\"\",\"answer_one_points\":\"0\",\"answer_two\":\"\",\"answer_two_points\":\"0\",\"answer_three\":\"\",\"answer_three_points\":\"0\",\"answer_four\":\"\",\"answer_four_points\":\"0\",\"answer_five\":\"\",\"answer_five_points\":\"0\",\"answer_six\":\"\",\"answer_six_points\":\"0\",\"correct_answer\":\"0\",\"question_answer_info\":\"\",\"comments\":\"1\",\"hints\":\"\",\"question_order\":\"0\",\"question_type\":\"0\",\"question_type_new\":\"0\",\"question_settings\":\"a:13:{s:14:\\\"question_title\\\";s:10:\\\"Question 9\\\";s:8:\\\"required\\\";i:0;s:12:\\\"answerEditor\\\";s:4:\\\"text\\\";s:15:\\\"featureImageSrc\\\";s:0:\\\"\\\";s:11:\\\"matchAnswer\\\";s:6:\\\"random\\\";s:14:\\\"case_sensitive\\\";s:0:\\\"\\\";s:14:\\\"answer_columns\\\";s:0:\\\"\\\";s:16:\\\"image_size-width\\\";s:0:\\\"\\\";s:17:\\\"image_size-height\\\";s:0:\\\"\\\";s:8:\\\"autofill\\\";s:0:\\\"\\\";s:23:\\\"limit_multiple_response\\\";s:0:\\\"\\\";s:17:\\\"file_upload_limit\\\";s:0:\\\"\\\";s:16:\\\"file_upload_type\\\";s:0:\\\"\\\";}\",\"category\":\"\",\"linked_question\":\"\",\"deleted\":\"0\",\"deleted_question_bank\":\"0\",\"answers\":[{\"0\":\"Dysfunction in the 5' cap recognition machinery of mRNA leads to enhanced cap-binding, resulting in increased mRNA stability and protein translation, causing hyperproliferative disorders.\",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"},{\"0\":\"Abnormalities in RNA-binding proteins that mediate alternative splicing result in improper splice site selection, leading to the production of non-functional protein isoforms and contributing to neurodegenerative disorders.\",\"1\":\"\",\"2\":\"1\",\"3\":\"\",\"label\":\"\"},{\"0\":\"Disruptions in the polyadenylation signal sequences of pre-mRNA transcripts lead to premature polyadenylation, resulting in truncated mRNA transcripts and subsequent mRNA degradation.\",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"},{\"0\":\"Dysregulation of the RNA-induced silencing complex components leads to enhanced microRNA-mediated gene silencing, resulting in the downregulation of critical tumor suppressor genes, contributing to oncogenesis.\",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"}]},\"164\":{\"question_id\":\"164\",\"quiz_id\":\"14\",\"question_name\":\"In which specific region of the DMPK (Dystrophia Myotonica Protein Kinase) gene are the runs of multiple CUG triplets located?\",\"answer_array\":\"a:4:{i:0;a:5:{i:0;s:170:\\\"The 3' untranslated region, causing RNA toxicity and sequestration of RNA-binding proteins, leading to impaired RNA metabolism and the pathogenesis of myotonic dystrophy.\\\";i:1;s:0:\\\"\\\";i:2;s:1:\\\"1\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:1;a:5:{i:0;s:136:\\\"The enhancer region, leading to a strong interaction with transcription factors, promoting excessive transcription of the DMPK protein. \\\";i:1;s:0:\\\"\\\";i:2;s:0:\\\"\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:2;a:5:{i:0;s:119:\\\"The 5' untranslated region, interfering with translational initiation and impairing the synthesis of the DMPK protein. \\\";i:1;s:0:\\\"\\\";i:2;s:0:\\\"\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}i:3;a:5:{i:0;s:111:\\\"The promoter region, leading to abnormal transcriptional activation and an overexpression of the DMPK protein. \\\";i:1;s:0:\\\"\\\";i:2;s:0:\\\"\\\";i:3;s:0:\\\"\\\";s:5:\\\"label\\\";s:0:\\\"\\\";}}\",\"answer_one\":\"\",\"answer_one_points\":\"0\",\"answer_two\":\"\",\"answer_two_points\":\"0\",\"answer_three\":\"\",\"answer_three_points\":\"0\",\"answer_four\":\"\",\"answer_four_points\":\"0\",\"answer_five\":\"\",\"answer_five_points\":\"0\",\"answer_six\":\"\",\"answer_six_points\":\"0\",\"correct_answer\":\"0\",\"question_answer_info\":\"\",\"comments\":\"1\",\"hints\":\"\",\"question_order\":\"0\",\"question_type\":\"0\",\"question_type_new\":\"0\",\"question_settings\":\"a:13:{s:14:\\\"question_title\\\";s:11:\\\"Question 10\\\";s:8:\\\"required\\\";i:0;s:12:\\\"answerEditor\\\";s:4:\\\"text\\\";s:15:\\\"featureImageSrc\\\";s:0:\\\"\\\";s:11:\\\"matchAnswer\\\";s:6:\\\"random\\\";s:14:\\\"case_sensitive\\\";s:0:\\\"\\\";s:14:\\\"answer_columns\\\";s:0:\\\"\\\";s:16:\\\"image_size-width\\\";s:0:\\\"\\\";s:17:\\\"image_size-height\\\";s:0:\\\"\\\";s:8:\\\"autofill\\\";s:0:\\\"\\\";s:23:\\\"limit_multiple_response\\\";s:0:\\\"\\\";s:17:\\\"file_upload_limit\\\";s:0:\\\"\\\";s:16:\\\"file_upload_type\\\";s:0:\\\"\\\";}\",\"category\":\"\",\"linked_question\":\"\",\"deleted\":\"0\",\"deleted_question_bank\":\"0\",\"answers\":[{\"0\":\"The 3' untranslated region, causing RNA toxicity and sequestration of RNA-binding proteins, leading to impaired RNA metabolism and the pathogenesis of myotonic dystrophy.\",\"1\":\"\",\"2\":\"1\",\"3\":\"\",\"label\":\"\"},{\"0\":\"The enhancer region, leading to a strong interaction with transcription factors, promoting excessive transcription of the DMPK protein. \",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"},{\"0\":\"The 5' untranslated region, interfering with translational initiation and impairing the synthesis of the DMPK protein. \",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"},{\"0\":\"The promoter region, leading to abnormal transcriptional activation and an overexpression of the DMPK protein. \",\"1\":\"\",\"2\":\"\",\"3\":\"\",\"label\":\"\"}]}},\"first_page\":false,\"questions_settings\":[]}\n                    <\/script>\t\t<div class='qsm-quiz-container qsm-quiz-container-14 qmn_quiz_container mlw_qmn_quiz qsm_auto_pagination_enabled quiz_theme_default  '>\n\t\t\t\t\t\t\t\t<form name=\"quizForm14\" id=\"quizForm14\" action=\"\/genecontrol\/wp-json\/wp\/v2\/content\/99\" method=\"POST\" class=\"qsm-quiz-form qmn_quiz_form mlw_quiz_form\" novalidate enctype=\"multipart\/form-data\">\n\t\t\t\t<input type=\"hidden\" name=\"qsm_hidden_questions\" id=\"qsm_hidden_questions\" value=\"\">\n\t\t\t\t<input type=\"hidden\" name=\"qsm_nonce\" id=\"qsm_nonce_14\" value=\"5c83811db2\">\n\t\t\t\t<input type=\"hidden\" name=\"qsm_unique_key\" id=\"qsm_unique_key_14\" value=\"69fca03b395c5\">\n\t\t\t\t<div id=\"mlw_error_message\" class=\"qsm-error-message qmn_error_message_section\"><\/div>\n\t\t\t\t<span id=\"mlw_top_of_quiz\"><\/span>\n\t\t\t\t\t\t\t\t\t<div class=\"qsm-auto-page-row qsm-question-page qsm-apc-1\" data-apid=\"1\" data-qpid=\"1\" style=\"display: none;\">\n\t\t\t\t\t\t\t\t<div class=\"quiz_section qsm-question-wrapper question-type-0  question-section-id-155 slide0 \">\n\t\t\t\t\t\t<div class='mlw_qmn_new_question'>Question 1 <\/div>\n\t\t\t\t\t<div class=\"qsm-featured-image\"><\/div>\n\t\t\t\t<div class='mlw_qmn_question  qsm_remove_bold' >\n\t\t<p>Which of the following options best completes the sentence: Disturbances in a factor involved in RNA processing lead to _______________________________ of a critical receptor gene<\/p>\n\t<\/div>\n\t\t<fieldset>\n\t\t<legend><\/legend>\n\t<div class='qmn_radio_answers mlwRequiredRadio'>\n\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question155-1 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question155\" id=\"question155_1\" value=\"0\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question155_1\">\n\t\t\t\t\timpaired mRNA processing\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question155-2 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question155\" id=\"question155_2\" value=\"1\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question155_2\">\n\t\t\t\t\taltered alternative splicing\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question155-3 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question155\" id=\"question155_3\" value=\"2\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question155_3\">\n\t\t\t\t\tenhanced expression\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question155-4 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question155\" id=\"question155_4\" value=\"3\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question155_4\">\n\t\t\t\t\tdecreased expression\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t \t\t\t<label style=\"display: none !important;\" for=\"question155_none\">None<\/label>\n\t\t\t<input type=\"radio\" style=\"display: none;\" name=\"question155\" id=\"question155_none\" checked=\"checked\" value=\"\" \/>\n\t\t\t\t<\/div>\n\t<\/fieldset>\n\t<input type=\"hidden\" name=\"answer_limit_keys_155\" value=\"\" \/>\n\t\t\t\t<\/div><!-- .quiz_section -->\n\t\t\t\t\t\t\t\t<\/div><!-- .qsm-auto-page-row -->\n\t\t\t\t\t\t\t\t\t\t<div class=\"qsm-auto-page-row qsm-question-page qsm-apc-2\" data-apid=\"2\" data-qpid=\"2\" style=\"display: none;\">\n\t\t\t\t\t\t\t\t<div class=\"quiz_section qsm-question-wrapper question-type-0  question-section-id-156 slide1 \">\n\t\t\t\t\t\t<div class='mlw_qmn_new_question'>Question 2 <\/div>\n\t\t\t<div class='mlw_qmn_question  qsm_remove_bold' >\n\t\t<p>Which of the following best describes the dominant nature of the Pax6 mutation?<\/p>\n\t<\/div>\n\t\t<fieldset>\n\t\t<legend><\/legend>\n\t<div class='qmn_radio_answers mlwRequiredRadio'>\n\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question156-1 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question156\" id=\"question156_1\" value=\"0\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question156_1\">\n\t\t\t\t\tThe Pax6 mutation leads to an enhanced production of the mutant protein, which exerts a dominant negative effect on the wild-type protein, inhibiting its normal function.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question156-2 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question156\" id=\"question156_2\" value=\"1\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question156_2\">\n\t\t\t\t\tThe dominant nature of the Pax6 mutation is attributed to the formation of heterodimers between the mutant and wild-type proteins, leading to an increased stability and enhanced activation of target genes.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question156-3 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question156\" id=\"question156_3\" value=\"2\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question156_3\">\n\t\t\t\t\tHaploid insufficiency is the underlying cause of the Pax6 mutation&#8217;s dominance, as a single functional copy of the gene cannot produce sufficient protein to effectively activate its target genes.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question156-4 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question156\" id=\"question156_4\" value=\"3\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question156_4\">\n\t\t\t\t\tThe Pax6 mutation triggers a gain-of-function effect, causing the mutant protein to be hyperactive and override the normal function of the wild-type protein.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t \t\t\t<label style=\"display: none !important;\" for=\"question156_none\">None<\/label>\n\t\t\t<input type=\"radio\" style=\"display: none;\" name=\"question156\" id=\"question156_none\" checked=\"checked\" value=\"\" \/>\n\t\t\t\t<\/div>\n\t<\/fieldset>\n\t<input type=\"hidden\" name=\"answer_limit_keys_156\" value=\"\" \/>\n\t\t\t\t<\/div><!-- .quiz_section -->\n\t\t\t\t\t\t\t\t<\/div><!-- .qsm-auto-page-row -->\n\t\t\t\t\t\t\t\t\t\t<div class=\"qsm-auto-page-row qsm-question-page qsm-apc-3\" data-apid=\"3\" data-qpid=\"3\" style=\"display: none;\">\n\t\t\t\t\t\t\t\t<div class=\"quiz_section qsm-question-wrapper question-type-0  question-section-id-157 slide2 \">\n\t\t\t\t\t\t<div class='mlw_qmn_new_question'>Question 3 <\/div>\n\t\t\t<div class='mlw_qmn_question  qsm_remove_bold' >\n\t\t<p>Mutations within an enhancer located 25 kb upstream of the PTF1A gene leads to\u2026?<\/p>\n\t<\/div>\n\t\t<fieldset>\n\t\t<legend><\/legend>\n\t<div class='qmn_radio_answers mlwRequiredRadio'>\n\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question157-1 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question157\" id=\"question157_1\" value=\"0\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question157_1\">\n\t\t\t\t\tdisruption of transcription factor binding, resulting in reduced PTF1A gene expression and pancreatic hypoplasia.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question157-2 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question157\" id=\"question157_2\" value=\"1\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question157_2\">\n\t\t\t\t\thyperactivation of the PTF1A gene, resulting in excessive pancreatic development and hypertrophy.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question157-3 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question157\" id=\"question157_3\" value=\"2\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question157_3\">\n\t\t\t\t\tsuppression of the PTF1A gene, leading to impaired pancreatic exocrine function and exocrine pancreas insufficiency.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question157-4 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question157\" id=\"question157_4\" value=\"3\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question157_4\">\n\t\t\t\t\talternative splicing of the PTF1A gene, leading to the formation of a non-functional protein and the development of pancreatic agenesis.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t \t\t\t<label style=\"display: none !important;\" for=\"question157_none\">None<\/label>\n\t\t\t<input type=\"radio\" style=\"display: none;\" name=\"question157\" id=\"question157_none\" checked=\"checked\" value=\"\" \/>\n\t\t\t\t<\/div>\n\t<\/fieldset>\n\t<input type=\"hidden\" name=\"answer_limit_keys_157\" value=\"\" \/>\n\t\t\t\t<\/div><!-- .quiz_section -->\n\t\t\t\t\t\t\t\t<\/div><!-- .qsm-auto-page-row -->\n\t\t\t\t\t\t\t\t\t\t<div class=\"qsm-auto-page-row qsm-question-page qsm-apc-4\" data-apid=\"4\" data-qpid=\"4\" style=\"display: none;\">\n\t\t\t\t\t\t\t\t<div class=\"quiz_section qsm-question-wrapper question-type-0  question-section-id-158 slide3 \">\n\t\t\t\t\t\t<div class='mlw_qmn_new_question'>Question 4 <\/div>\n\t\t\t<div class='mlw_qmn_question  qsm_remove_bold' >\n\t\t<p>What is the consequence of having a single inactive CBP gene?<\/p>\n\t<\/div>\n\t\t<fieldset>\n\t\t<legend><\/legend>\n\t<div class='qmn_radio_answers mlwRequiredRadio'>\n\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question158-1 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question158\" id=\"question158_1\" value=\"0\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question158_1\">\n\t\t\t\t\tAbnormal embryonic development and organogenesis, leading to early embryonic lethality.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question158-2 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question158\" id=\"question158_2\" value=\"1\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question158_2\">\n\t\t\t\t\tImpaired chromatin remodeling and DNA repair mechanisms, causing widespread genomic instability and cell death.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question158-3 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question158\" id=\"question158_3\" value=\"2\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question158_3\">\n\t\t\t\t\tUncontrolled cell proliferation and tumor development.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question158-4 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question158\" id=\"question158_4\" value=\"3\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question158_4\">\n\t\t\t\t\tRubinstein-Taybi syndrome characterized by mental and physical abnormalities due to impaired neural development and gene regulation.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t \t\t\t<label style=\"display: none !important;\" for=\"question158_none\">None<\/label>\n\t\t\t<input type=\"radio\" style=\"display: none;\" name=\"question158\" id=\"question158_none\" checked=\"checked\" value=\"\" \/>\n\t\t\t\t<\/div>\n\t<\/fieldset>\n\t<input type=\"hidden\" name=\"answer_limit_keys_158\" value=\"\" \/>\n\t\t\t\t<\/div><!-- .quiz_section -->\n\t\t\t\t\t\t\t\t<\/div><!-- .qsm-auto-page-row -->\n\t\t\t\t\t\t\t\t\t\t<div class=\"qsm-auto-page-row qsm-question-page qsm-apc-5\" data-apid=\"5\" data-qpid=\"5\" style=\"display: none;\">\n\t\t\t\t\t\t\t\t<div class=\"quiz_section qsm-question-wrapper question-type-0  question-section-id-159 slide4 \">\n\t\t\t\t\t\t<div class='mlw_qmn_new_question'>Question 5 <\/div>\n\t\t\t<div class='mlw_qmn_question  qsm_remove_bold' >\n\t\t<p>How does the presence of mutant Huntingtin lead to disease development in Huntington\\&#8217;s disease?<\/p>\n\t<\/div>\n\t\t<fieldset>\n\t\t<legend><\/legend>\n\t<div class='qmn_radio_answers mlwRequiredRadio'>\n\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question159-1 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question159\" id=\"question159_1\" value=\"0\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question159_1\">\n\t\t\t\t\tIt forms toxic aggregates that impair cellular trafficking and disrupt organelle function, leading to neuronal dysfunction and neurodegeneration.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question159-2 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question159\" id=\"question159_2\" value=\"1\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question159_2\">\n\t\t\t\t\tIt enhances the activity of proteasomes, leading to excessive degradation of essential proteins and cellular dysfunction.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question159-3 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question159\" id=\"question159_3\" value=\"2\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question159_3\">\n\t\t\t\t\tIt directly binds to DNA promoter regions, causing aberrant gene activation and uncontrolled cell proliferation.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question159-4 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question159\" id=\"question159_4\" value=\"3\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question159_4\">\n\t\t\t\t\tMutant Huntingtin stimulates hyperphosphorylation of neurotransmitter receptors, resulting in impaired synaptic transmission and cognitive decline.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t \t\t\t<label style=\"display: none !important;\" for=\"question159_none\">None<\/label>\n\t\t\t<input type=\"radio\" style=\"display: none;\" name=\"question159\" id=\"question159_none\" checked=\"checked\" value=\"\" \/>\n\t\t\t\t<\/div>\n\t<\/fieldset>\n\t<input type=\"hidden\" name=\"answer_limit_keys_159\" value=\"\" \/>\n\t\t\t\t<\/div><!-- .quiz_section -->\n\t\t\t\t\t\t\t\t<\/div><!-- .qsm-auto-page-row -->\n\t\t\t\t\t\t\t\t\t\t<div class=\"qsm-auto-page-row qsm-question-page qsm-apc-6\" data-apid=\"6\" data-qpid=\"6\" style=\"display: none;\">\n\t\t\t\t\t\t\t\t<div class=\"quiz_section qsm-question-wrapper question-type-0  question-section-id-160 slide5 \">\n\t\t\t\t\t\t<div class='mlw_qmn_new_question'>Question 6 <\/div>\n\t\t\t<div class='mlw_qmn_question  qsm_remove_bold' >\n\t\t<p>What is the  underlying cause of the rare human ICF syndrome?<\/p>\n\t<\/div>\n\t\t<fieldset>\n\t\t<legend><\/legend>\n\t<div class='qmn_radio_answers mlwRequiredRadio'>\n\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question160-1 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question160\" id=\"question160_1\" value=\"0\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question160_1\">\n\t\t\t\t\tMutations in the DNA repair genes, specifically those involved in base excision repair, leading to the accumulation of DNA damage and chromosomal instability.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question160-2 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question160\" id=\"question160_2\" value=\"1\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question160_2\">\n\t\t\t\t\tAbnormal DNA methylation patterns resulting from mutations in the DNA methyltransferase genes, leading to genomic instability and altered gene expression.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question160-3 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question160\" id=\"question160_3\" value=\"2\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question160_3\">\n\t\t\t\t\tDeletions in the genes encoding structural proteins involved in centromere formation, leading to impaired chromosome segregation and centromeric instability.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question160-4 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question160\" id=\"question160_4\" value=\"3\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question160_4\">\n\t\t\t\t\tDeficiencies in the components of the RNA interference (RNAi) pathway, leading to uncontrolled gene expression and dysregulation of immune-related genes.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t \t\t\t<label style=\"display: none !important;\" for=\"question160_none\">None<\/label>\n\t\t\t<input type=\"radio\" style=\"display: none;\" name=\"question160\" id=\"question160_none\" checked=\"checked\" value=\"\" \/>\n\t\t\t\t<\/div>\n\t<\/fieldset>\n\t<input type=\"hidden\" name=\"answer_limit_keys_160\" value=\"\" \/>\n\t\t\t\t<\/div><!-- .quiz_section -->\n\t\t\t\t\t\t\t\t<\/div><!-- .qsm-auto-page-row -->\n\t\t\t\t\t\t\t\t\t\t<div class=\"qsm-auto-page-row qsm-question-page qsm-apc-7\" data-apid=\"7\" data-qpid=\"7\" style=\"display: none;\">\n\t\t\t\t\t\t\t\t<div class=\"quiz_section qsm-question-wrapper question-type-0  question-section-id-161 slide6 \">\n\t\t\t\t\t\t<div class='mlw_qmn_new_question'>Question 7 <\/div>\n\t\t\t<div class='mlw_qmn_question  qsm_remove_bold' >\n\t\t<p>How does the inactivation of JARID1C interfere with the ability of REST (RE1-silencing transcription factor) to repress gene expression?<\/p>\n\t<\/div>\n\t\t<fieldset>\n\t\t<legend><\/legend>\n\t<div class='qmn_radio_answers mlwRequiredRadio'>\n\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question161-1 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question161\" id=\"question161_1\" value=\"0\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question161_1\">\n\t\t\t\t\tThis leads to abnormal DNA methylation at the RE1 binding sites, preventing REST from binding to its target genes and relieving transcriptional repression.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question161-2 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question161\" id=\"question161_2\" value=\"1\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question161_2\">\n\t\t\t\t\tJARID1C physically interacts with REST and recruits co-repressor complexes to the promoter regions of target genes, thereby enhancing REST-mediated transcriptional repression.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question161-3 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question161\" id=\"question161_3\" value=\"2\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question161_3\">\n\t\t\t\t\tThis disrupts the nuclear localization of REST, preventing it from entering the nucleus and executing its transcriptional repression functions.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question161-4 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question161\" id=\"question161_4\" value=\"3\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question161_4\">\n\t\t\t\t\tJARID1C acts as a histone demethylase, removing repressive histone marks at the promoter regions of REST target genes, resulting in increased gene expression.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t \t\t\t<label style=\"display: none !important;\" for=\"question161_none\">None<\/label>\n\t\t\t<input type=\"radio\" style=\"display: none;\" name=\"question161\" id=\"question161_none\" checked=\"checked\" value=\"\" \/>\n\t\t\t\t<\/div>\n\t<\/fieldset>\n\t<input type=\"hidden\" name=\"answer_limit_keys_161\" value=\"\" \/>\n\t\t\t\t<\/div><!-- .quiz_section -->\n\t\t\t\t\t\t\t\t<\/div><!-- .qsm-auto-page-row -->\n\t\t\t\t\t\t\t\t\t\t<div class=\"qsm-auto-page-row qsm-question-page qsm-apc-8\" data-apid=\"8\" data-qpid=\"8\" style=\"display: none;\">\n\t\t\t\t\t\t\t\t<div class=\"quiz_section qsm-question-wrapper question-type-0  question-section-id-162 slide7 \">\n\t\t\t\t\t\t<div class='mlw_qmn_new_question'>Question 8 <\/div>\n\t\t\t<div class='mlw_qmn_question  qsm_remove_bold' >\n\t\t<p>A mutation in the SNF2 factor, which is a vital component of the chromatin-remodeling SWI\/SNF complex, can lead to \u03b1-thalassemia combined with mental retardation. This observation suggests that SNF2\\&#8217;s activity is essential for:<\/p>\n\t<\/div>\n\t\t<fieldset>\n\t\t<legend><\/legend>\n\t<div class='qmn_radio_answers mlwRequiredRadio'>\n\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question162-1 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question162\" id=\"question162_1\" value=\"0\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question162_1\">\n\t\t\t\t\tFacilitating DNA replication by promoting the unwinding of the double helix, allowing the DNA polymerase access to the template strand.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question162-2 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question162\" id=\"question162_2\" value=\"1\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question162_2\">\n\t\t\t\t\tRecruiting transcription factors to gene promoter regions, enhancing gene expression and promoting transcriptional activation.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question162-3 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question162\" id=\"question162_3\" value=\"2\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question162_3\">\n\t\t\t\t\tOpening the chromatin structure of the \u03b1-globin genes and other genes, allowing transcriptional machinery access and enabling gene expression.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question162-4 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question162\" id=\"question162_4\" value=\"3\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question162_4\">\n\t\t\t\t\tMediating post-translational modifications of histone proteins, influencing chromatin condensation and regulating gene silencing.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t \t\t\t<label style=\"display: none !important;\" for=\"question162_none\">None<\/label>\n\t\t\t<input type=\"radio\" style=\"display: none;\" name=\"question162\" id=\"question162_none\" checked=\"checked\" value=\"\" \/>\n\t\t\t\t<\/div>\n\t<\/fieldset>\n\t<input type=\"hidden\" name=\"answer_limit_keys_162\" value=\"\" \/>\n\t\t\t\t<\/div><!-- .quiz_section -->\n\t\t\t\t\t\t\t\t<\/div><!-- .qsm-auto-page-row -->\n\t\t\t\t\t\t\t\t\t\t<div class=\"qsm-auto-page-row qsm-question-page qsm-apc-9\" data-apid=\"9\" data-qpid=\"9\" style=\"display: none;\">\n\t\t\t\t\t\t\t\t<div class=\"quiz_section qsm-question-wrapper question-type-0  question-section-id-163 slide8 \">\n\t\t\t\t\t\t<div class='mlw_qmn_new_question'>Question 9 <\/div>\n\t\t\t<div class='mlw_qmn_question  qsm_remove_bold' >\n\t\t<p>How can alterations in specific post-transcriptional stages of gene regulation contribute to the development of human disease?<\/p>\n\t<\/div>\n\t\t<fieldset>\n\t\t<legend><\/legend>\n\t<div class='qmn_radio_answers mlwRequiredRadio'>\n\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question163-1 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question163\" id=\"question163_1\" value=\"0\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question163_1\">\n\t\t\t\t\tDysfunction in the 5&#8242; cap recognition machinery of mRNA leads to enhanced cap-binding, resulting in increased mRNA stability and protein translation, causing hyperproliferative disorders.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question163-2 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question163\" id=\"question163_2\" value=\"1\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question163_2\">\n\t\t\t\t\tAbnormalities in RNA-binding proteins that mediate alternative splicing result in improper splice site selection, leading to the production of non-functional protein isoforms and contributing to neurodegenerative disorders.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question163-3 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question163\" id=\"question163_3\" value=\"2\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question163_3\">\n\t\t\t\t\tDisruptions in the polyadenylation signal sequences of pre-mRNA transcripts lead to premature polyadenylation, resulting in truncated mRNA transcripts and subsequent mRNA degradation.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question163-4 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question163\" id=\"question163_4\" value=\"3\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question163_4\">\n\t\t\t\t\tDysregulation of the RNA-induced silencing complex components leads to enhanced microRNA-mediated gene silencing, resulting in the downregulation of critical tumor suppressor genes, contributing to oncogenesis.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t \t\t\t<label style=\"display: none !important;\" for=\"question163_none\">None<\/label>\n\t\t\t<input type=\"radio\" style=\"display: none;\" name=\"question163\" id=\"question163_none\" checked=\"checked\" value=\"\" \/>\n\t\t\t\t<\/div>\n\t<\/fieldset>\n\t<input type=\"hidden\" name=\"answer_limit_keys_163\" value=\"\" \/>\n\t\t\t\t<\/div><!-- .quiz_section -->\n\t\t\t\t\t\t\t\t<\/div><!-- .qsm-auto-page-row -->\n\t\t\t\t\t\t\t\t\t\t<div class=\"qsm-auto-page-row qsm-question-page qsm-apc-10\" data-apid=\"10\" data-qpid=\"10\" style=\"display: none;\">\n\t\t\t\t\t\t\t\t<div class=\"quiz_section qsm-question-wrapper question-type-0  question-section-id-164 slide9 \">\n\t\t\t\t\t\t<div class='mlw_qmn_new_question'>Question 10 <\/div>\n\t\t\t<div class='mlw_qmn_question  qsm_remove_bold' >\n\t\t<p>In which specific region of the DMPK (Dystrophia Myotonica Protein Kinase) gene are the runs of multiple CUG triplets located?<\/p>\n\t<\/div>\n\t\t<fieldset>\n\t\t<legend><\/legend>\n\t<div class='qmn_radio_answers mlwRequiredRadio'>\n\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question164-1 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question164\" id=\"question164_1\" value=\"0\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question164_1\">\n\t\t\t\t\tThe 3&#8242; untranslated region, causing RNA toxicity and sequestration of RNA-binding proteins, leading to impaired RNA metabolism and the pathogenesis of myotonic dystrophy.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question164-2 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question164\" id=\"question164_2\" value=\"1\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question164_2\">\n\t\t\t\t\tThe enhancer region, leading to a strong interaction with transcription factors, promoting excessive transcription of the DMPK protein.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question164-3 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question164\" id=\"question164_3\" value=\"2\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question164_3\">\n\t\t\t\t\tThe 5&#8242; untranslated region, interfering with translational initiation and impairing the synthesis of the DMPK protein.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t<div class=\"qmn_mc_answer_wrap  mrq_checkbox_class\" id=\"question164-4 \">\n\t\t\t\t\t\t\t\t\t\t\t<input type='radio' class='qmn_quiz_radio qmn-multiple-choice-input ' name=\"question164\" id=\"question164_4\" value=\"3\" \/>\n\t\t\t\t\t<label class=\"qsm-input-label\" for=\"question164_4\">\n\t\t\t\t\tThe promoter region, leading to abnormal transcriptional activation and an overexpression of the DMPK protein.\t\t\t\t\t<\/label>\n\t\t\t\t\t \t\t\t\t<\/div>\n\t\t\t\t\t \t\t\t<label style=\"display: none !important;\" for=\"question164_none\">None<\/label>\n\t\t\t<input type=\"radio\" style=\"display: none;\" name=\"question164\" id=\"question164_none\" checked=\"checked\" value=\"\" \/>\n\t\t\t\t<\/div>\n\t<\/fieldset>\n\t<input type=\"hidden\" name=\"answer_limit_keys_164\" value=\"\" \/>\n\t\t\t\t<\/div><!-- .quiz_section -->\n\t\t\t\t\t\t\t\t<\/div><!-- .qsm-auto-page-row -->\n\t\t\t\t\t\t\t<input type=\"hidden\" name=\"qmn_question_list\" value=\"155Q156Q157Q158Q159Q160Q161Q162Q163Q164Q\" \/>\n\t\t\t\t\t<div class=\"qsm-auto-page-row quiz_section quiz_end empty_quiz_end qsm-d-none\" >\n\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<div id=\"mlw_error_message_bottom\" class=\"qsm-error-message qmn_error_message_section\"><\/div>\n\t\t\t\t\t<input type=\"hidden\" name=\"qmn_all_questions_count\" id=\"qmn_all_questions_count\" value=\"10\" \/>\n\t\t\t\t\t<input type=\"hidden\" name=\"total_questions\" id=\"total_questions\" value=\"10\" \/>\n\t\t\t\t\t<input type=\"hidden\" name=\"timer\" id=\"timer\" value=\"0\" \/>\n\t\t\t\t\t<input type=\"hidden\" name=\"timer_ms\" id=\"timer_ms\" value=\"0\"\/>\n\t\t\t\t\t<input type=\"hidden\" class=\"qmn_quiz_id\" name=\"qmn_quiz_id\" id=\"qmn_quiz_id\" value=\"14\" \/>\n\t\t\t\t\t<input type='hidden' name='complete_quiz' value='confirmation' \/>\n\t\t\t\t\t\t\t\t\t<\/form>\n\t\t\t\t\t\t<\/div>\n\t\t<div style=\"display: none;\" class=\"qsm-popup qsm-popup-slide\" id=\"modal-4\" aria-hidden=\"false\"><div class=\"qsm-popup__overlay\" tabindex=\"-1\" data-micromodal-close=\"\"><div class=\"qsm-popup__container qmn_quiz_container\" role=\"dialog\" aria-modal=\"true\"><div class=\"qsm-popup__content\"><img decoding=\"async\" src=\"https:\/\/staging.routledgelearning.com\/genecontrol\/wp-content\/plugins\/quiz-master-next\/assets\/clock.png\" alt=\"clock.png\"\/><p class=\"qsm-time-up-text\"> Time&#8217;s up<\/p><\/div><footer class=\"qsm-popup__footer\"><button class=\"qsm-popup-secondary-button qmn_btn\" data-micromodal-close=\"\" aria-label=\"Close this dialog window\" onclick=\"location.reload();\">Cancel<\/button><\/footer><\/div><\/div><\/div>\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<h2 class=\"wp-block-heading alignwide\" id=\"aioseo-questions-for-discussion\">Questions for Discussion<\/h2>\n\n\n\n<ol class=\"wp-block-list\">\n<li>Trinucleotide repeat expansions (TNREs) are linked to a variety of inherited human diseases. Describe a specific type of TNREs that encode codons for long stretch of an amino acid in its coding sequence. Do you think this TNRE sequence will prevent the RNA polymerase from transcribing it? Also, If an individual has a mild form of a TNRE disorder, what factors should this person consider for future offspring?<\/li>\n\n\n\n<li>Several research studies are underway that involve the use of gene therapies for several diseases. Discuss the advantages and disadvantages of gene therapies and the potential implications on evolution that scientists and society should consider before the approval of gene therapies.<\/li>\n\n\n\n<li>Discuss the paradoxical role of the innate immune system, such as interferon signaling, in antiviral, antitumor, and procancer functions.<\/li>\n\n\n\n<li>Discuss the role of epigenetic processes in neuroinflammation and its effect on neuronal regeneration.<\/li>\n\n\n\n<li>Discuss the role of non-coding RNA in chronic disease such as multiple sclerosis, Alzhiemers, and diabetes.<\/li>\n<\/ol>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"aioseo-further-reading\">Further Reading<\/h2>\n\n\n\n<details class=\"wp-block-details is-layout-flow wp-block-details-is-layout-flow\"><summary>14.1 Transcription and human disease<\/summary>\n<p>Claringbould, A., &amp; Zaugg, J. B. (2021). Enhancers in disease: Molecular basis and emerging treatment strategies. Trends in Molecular Medicine, 27(11), 1060\u20131073. <a href=\"https:\/\/doi.org\/10.1016\/j.molmed.2021.07.012\">https:\/\/doi.org\/10.1016\/j.molmed.2021.07.012<\/a><\/p>\n\n\n\n<p>Degtyareva, A. O., Antontseva, E. V., &amp; Merkulova, T. I. (2021). Regulatory SNPs: Altered Transcription Factor Binding Sites Implicated in Complex Traits and Diseases. International Journal of Molecular Sciences, 22(12), 6454. <a href=\"https:\/\/doi.org\/10.3390\/ijms22126454\">https:\/\/doi.org\/10.3390\/ijms22126454<\/a><\/p>\n\n\n\n<p>Kvon, E. Z., Waymack, R., Gad, M., &amp; Wunderlich, Z. (2021). Enhancer redundancy in development and disease. Nature Reviews. Genetics, 22(5), 324\u2013336. <a href=\"https:\/\/doi.org\/10.1038\/s41576-020-00311-x\">https:\/\/doi.org\/10.1038\/s41576-020-00311-x<\/a><\/p>\n\n\n\n<p>Lee T.I. &amp; Young R.A. (2013) Transcriptional regulation and its misregulation in disease. Cell 152:1237\u20131251.<br>Zaugg, J. B., Sahl\u00e9n, P., Andersson, R., Alberich-Jorda, M., de Laat, W., Deplancke, B., Ferrer, J., Mandrup, S., Natoli, G., Plewczynski, D., Rada-Iglesias, A., &amp; Spicuglia, S. (2022). Current challenges in understanding the role of enhancers in disease. Nature Structural &amp; Molecular Biology, 29(12), 1148\u20131158. <a href=\"https:\/\/doi.org\/10.1038\/s41594-022-00896-3\">https:\/\/doi.org\/10.1038\/s41594-022-00896-3<\/a><a><\/a><\/p>\n<\/details>\n\n\n\n<details class=\"wp-block-details is-layout-flow wp-block-details-is-layout-flow\"><summary>14.2 The epigenome and human disease<\/summary>\n<p>Aguilera, P., &amp; L\u00f3pez-Contreras, A. J. (2023). ATRX, a guardian of chromatin. Trends in Genetics: TIG, 39(6), 505\u2013519. <a href=\"https:\/\/doi.org\/10.1016\/j.tig.2023.02.009\">https:\/\/doi.org\/10.1016\/j.tig.2023.02.009<\/a><\/p>\n\n\n\n<p>Baccarelli, A., Dolinoy, D. C., &amp; Walker, C. L. (2023). A precision environmental health approach to prevention of human disease. Nature Communications, 14(1), 2449. <a href=\"https:\/\/doi.org\/10.1038\/s41467-023-37626-2\">https:\/\/doi.org\/10.1038\/s41467-023-37626-2<\/a><\/p>\n\n\n\n<p>Dyer, M. A., Qadeer, Z. A., Valle-Garcia, D., &amp; Bernstein, E. (2017). ATRX and DAXX: Mechanisms and Mutations. Cold Spring Harbor Perspectives in Medicine, 7(3), a026567. <a href=\"https:\/\/doi.org\/10.1101\/cshperspect.a026567\">https:\/\/doi.org\/10.1101\/cshperspect.a026567<\/a><\/p>\n\n\n\n<p>Han, V. X., Patel, S., Jones, H. F., &amp; Dale, R. C. (2021). Maternal immune activation and neuroinflammation in human neurodevelopmental disorders. Nature Reviews. Neurology, 17(9), 564\u2013579. <a href=\"https:\/\/doi.org\/10.1038\/s41582-021-00530-8\">https:\/\/doi.org\/10.1038\/s41582-021-00530-8<\/a><\/p>\n\n\n\n<p>Oh, E. S., &amp; Petronis, A. (2021). Origins of human disease: The chrono-epigenetic perspective. Nature Reviews. Genetics, 22(8), 533\u2013546. <a href=\"https:\/\/doi.org\/10.1038\/s41576-021-00348-6\">https:\/\/doi.org\/10.1038\/s41576-021-00348-6<\/a><\/p>\n\n\n\n<p>Richter, W. F., Nayak, S., Iwasa, J., &amp; Taatjes, D. J. (2022). The Mediator complex as a master regulator of transcription by RNA polymerase II. Nature Reviews Molecular Cell Biology, 23(11), 732\u2013749. <a href=\"https:\/\/doi.org\/10.1038\/s41580-022-00498-3\">https:\/\/doi.org\/10.1038\/s41580-022-00498-3<\/a><\/p>\n\n\n\n<p>Schiano, C., Luongo, L., Maione, S., &amp; Napoli, C. (2023). Mediator complex in neurological disease. Life Sciences, 329, 121986. <a href=\"https:\/\/doi.org\/10.1016\/j.lfs.2023.121986\">https:\/\/doi.org\/10.1016\/j.lfs.2023.121986<\/a><\/p>\n\n\n\n<p>Wu, H., Eckhardt, C. M., &amp; Baccarelli, A. A. (2023). Molecular mechanisms of environmental exposures and human disease. Nature Reviews. Genetics, 24(5), 332\u2013344. <a href=\"https:\/\/doi.org\/10.1038\/s41576-022-00569-3\">https:\/\/doi.org\/10.1038\/s41576-022-00569-3<\/a> <a><\/a><\/p>\n<\/details>\n\n\n\n<details class=\"wp-block-details is-layout-flow wp-block-details-is-layout-flow\"><summary>14.3 Post-transcriptional processes and human disease<\/summary>\n<p>Gy, L., &amp; Dm, S. (2020). mTOR at the nexus of nutrition, growth, ageing and disease. Nature Reviews. Molecular Cell Biology, 21(4). <a href=\"https:\/\/doi.org\/10.1038\/s41580-019-0199-y\">https:\/\/doi.org\/10.1038\/s41580-019-0199-y<\/a><\/p>\n\n\n\n<p>Hachiya, N., Sochocka, M., Brzecka, A., Shimizu, T., G\u0105siorowski, K., Szczechowiak, K., &amp; Leszek, J. (2021). Nuclear Envelope and Nuclear Pore Complexes in Neurodegenerative Diseases\u2014New Perspectives for Therapeutic Interventions. Molecular Neurobiology, 58(3), 983\u2013995. <a href=\"https:\/\/doi.org\/10.1007\/s12035-020-02168-x\">https:\/\/doi.org\/10.1007\/s12035-020-02168-x<\/a><\/p>\n\n\n\n<p>Jishi, A., Qi, X., &amp; Miranda, H. C. (2021). Implications of mRNA translation dysregulation for neurological disorders. Seminars in Cell &amp; Developmental Biology, 114, 11\u201319. <a href=\"https:\/\/doi.org\/10.1016\/j.semcdb.2020.09.005\">https:\/\/doi.org\/10.1016\/j.semcdb.2020.09.005<\/a><\/p>\n\n\n\n<p>L\u00f3pez-Mart\u00ednez, A., Soblechero-Mart\u00edn, P., de-la-Puente-Ovejero, L., Nogales-Gadea, G., &amp; Arechavala-Gomeza, V. (2020). An Overview of Alternative Splicing Defects Implicated in Myotonic Dystrophy Type I. Genes, 11(9), 1109. <a href=\"https:\/\/doi.org\/10.3390\/genes11091109\">https:\/\/doi.org\/10.3390\/genes11091109<\/a><\/p>\n\n\n\n<p>Moss, T., LeDoux, M. S., &amp; Crane-Robinson, C. (2023). HMG-boxes, ribosomopathies and neurodegenerative disease. Frontiers in Genetics, 14, 1225832. <a href=\"https:\/\/doi.org\/10.3389\/fgene.2023.1225832\">https:\/\/doi.org\/10.3389\/fgene.2023.1225832<\/a><\/p>\n\n\n\n<p>Nishimura, K., Yamazaki, H., Zang, W., &amp; Inoue, D. (2022). Dysregulated minor intron splicing in cancer. Cancer Science, 113(9), 2934\u20132942. <a href=\"https:\/\/doi.org\/10.1111\/cas.15476\">https:\/\/doi.org\/10.1111\/cas.15476<\/a><\/p>\n\n\n\n<p>Richter, J. D., &amp; Zhao, X. (2021). The molecular biology of FMRP: New insights into fragile X syndrome. Nature Reviews. Neuroscience, 22(4), 209\u2013222. <a href=\"https:\/\/doi.org\/10.1038\/s41583-021-00432-0\">https:\/\/doi.org\/10.1038\/s41583-021-00432-0<\/a><\/p>\n\n\n\n<p>Yang, Y., Guo, L., Chen, L., Gong, B., Jia, D., &amp; Sun, Q. (2023). Nuclear transport proteins: Structure, function, and disease relevance. Signal Transduction and Targeted Therapy, 8(1), 1\u201329. <a href=\"https:\/\/doi.org\/10.1038\/s41392-023-01649-4\">https:\/\/doi.org\/10.1038\/s41392-023-01649-4<\/a> <a><\/a><\/p>\n<\/details>\n\n\n\n<details class=\"wp-block-details is-layout-flow wp-block-details-is-layout-flow\"><summary>14.4 Regulatory RNAs and human disease<\/summary>\n<p>Ariyanfar, S., &amp; Good, D. J. (2022). Analysis of SNHG14: A Long Non-Coding RNA Hosting SNORD116, Whose Loss Contributes to Prader-Willi Syndrome Etiology. Genes, 14(1), 97. <a href=\"https:\/\/doi.org\/10.3390\/genes14010097\">https:\/\/doi.org\/10.3390\/genes14010097<\/a><\/p>\n\n\n\n<p>DiStefano, J. K., &amp; Gerhard, G. S. (2022). Long Noncoding RNAs and Human Liver Disease. Annual Review of Pathology, 17, 1\u201321. <a href=\"https:\/\/doi.org\/10.1146\/annurev-pathol-042320-115255\">https:\/\/doi.org\/10.1146\/annurev-pathol-042320-115255<\/a><\/p>\n\n\n\n<p>MacDonald, W. A., &amp; Mann, M. R. W. (2020). Long noncoding RNA functionality in imprinted domain regulation. PLOS Genetics, 16(8), e1008930. <a href=\"https:\/\/doi.org\/10.1371\/journal.pgen.1008930\">https:\/\/doi.org\/10.1371\/journal.pgen.1008930<\/a><\/p>\n\n\n\n<p>Mangiavacchi, A., Morelli, G., &amp; Orlando, V. (2023). Behind the scenes: How RNA orchestrates the epigenetic regulation of gene expression. Frontiers in Cell and Developmental Biology, 11. <a href=\"https:\/\/doi.org\/10.3389\/fcell.2023.1123975\">https:\/\/doi.org\/10.3389\/fcell.2023.1123975<\/a><\/p>\n\n\n\n<p>Nowak, A., Wicik, Z., Wolska, M., Shahzadi, A., Szwed, P., Jarosz-Popek, J., Palatini, J., Postula, M., Czlonkowska, A., Mirowska-Guzel, D., &amp; Eyileten, C. (2022). The role of non-coding RNAs in neuroinflammatory process in multiple sclerosis. Molecular Neurobiology, 59(8), 4651\u20134668. <a href=\"https:\/\/doi.org\/10.1007\/s12035-022-02854-y\">https:\/\/doi.org\/10.1007\/s12035-022-02854-y<\/a><\/p>\n\n\n\n<p>Ram\u00edrez, A. E., Gil-Jaramillo, N., Tapias, M. A., Gonz\u00e1lez-Giraldo, Y., Pinz\u00f3n, A., Puentes-Rozo, P. J., Aristiz\u00e1bal-Pach\u00f3n, A. F., &amp; Gonz\u00e1lez, J. (2022). MicroRNA: A Linking between Astrocyte Dysfunction, Mild Cognitive Impairment, and Neurodegenerative Diseases. Life (Basel, Switzerland), 12(9), 1439. <a href=\"https:\/\/doi.org\/10.3390\/life12091439%2014.5\">https:\/\/doi.org\/10.3390\/life12091439 14.5<\/a><a><\/a><\/p>\n<\/details>\n\n\n\n<details class=\"wp-block-details is-layout-flow wp-block-details-is-layout-flow\"><summary>14.5 Infectious diseases and cellular gene expression<\/summary>\n<p>Beyond Good and Evil: Molecular Mechanisms of Type I and III IFN Functions | The Journal of Immunology | American Association of Immunologists. (n.d.). Retrieved April 8, 2024, from <a href=\"https:\/\/journals.aai.org\/jimmunol\/article\/208\/2\/247\/234825\">https:\/\/journals.aai.org\/jimmunol\/article\/208\/2\/247\/234825<\/a><\/p>\n\n\n\n<p>Krischuns, T., Lukarska, M., Naffakh, N., &amp; Cusack, S. (2021). Influenza Virus RNA-Dependent RNA Polymerase and the Host Transcriptional Apparatus. Annual Review of Biochemistry, 90, 321\u2013348. <a href=\"https:\/\/doi.org\/10.1146\/annurev-biochem-072820-100645\">https:\/\/doi.org\/10.1146\/annurev-biochem-072820-100645<\/a><\/p>\n\n\n\n<p>Liang, Y., &amp; Wang, L. (2021). Inflamma-MicroRNAs in Alzheimer\u2019s Disease: From Disease Pathogenesis to Therapeutic Potentials. Frontiers in Cellular Neuroscience, 15, 785433. <a href=\"https:\/\/doi.org\/10.3389\/fncel.2021.785433\">https:\/\/doi.org\/10.3389\/fncel.2021.785433<\/a><\/p>\n\n\n\n<p>Mazewski, C., Perez, R. E., Fish, E. N., &amp; Platanias, L. C. (2020). Type I Interferon (IFN)-Regulated Activation of Canonical and Non-Canonical Signaling Pathways. Frontiers in Immunology, 11. <a href=\"https:\/\/doi.org\/10.3389\/fimmu.2020.606456\">https:\/\/doi.org\/10.3389\/fimmu.2020.606456<\/a><\/p>\n\n\n\n<p>Shehata, S. I., Watkins, J. M., Burke, J. M., &amp; Parker, R. (2024). Mechanisms and consequences of mRNA destabilization during viral infections. Virology Journal, 21(1), 38. <a href=\"https:\/\/doi.org\/10.1186\/s12985-024-02305-1\">https:\/\/doi.org\/10.1186\/s12985-024-02305-1<\/a><a><\/a><\/p>\n<\/details>\n\n\n\n<details class=\"wp-block-details is-layout-flow wp-block-details-is-layout-flow\"><summary>14.6 Gene regulation and therapy of human disease<\/summary>\n<p>El Marabti, E., &amp; Abdel-Wahab, O. (2021). Therapeutic Modulation of RNA Splicing in Malignant and Non-Malignant Disease. Trends in Molecular Medicine, 27(7), 643\u2013659. <a href=\"https:\/\/doi.org\/10.1016\/j.molmed.2021.04.005\">https:\/\/doi.org\/10.1016\/j.molmed.2021.04.005<\/a><\/p>\n\n\n\n<p>Frontiers | Regulatory Effects of Histone Deacetylase Inhibitors on Myeloid-Derived Suppressor Cells. (n.d.). Retrieved April 8, 2024, from <a href=\"https:\/\/www.frontiersin.org\/journals\/immunology\/articles\/10.3389\/fimmu.2021.690207\/full\">https:\/\/www.frontiersin.org\/journals\/immunology\/articles\/10.3389\/fimmu.2021.690207\/full<\/a><\/p>\n\n\n\n<p>Hartmann, D., Smith, J. M., Mazzotti, G., Chowdhry, R., &amp; Booth, M. J. (2020). Controlling gene expression with light: A multidisciplinary endeavour. Biochemical Society Transactions, 48(4), 1645\u20131659. <a href=\"https:\/\/doi.org\/10.1042\/BST20200014\">https:\/\/doi.org\/10.1042\/BST20200014<\/a><\/p>\n\n\n\n<p>Le Bl\u00e9vec, E., Muro\u0148ov\u00e1, J., Ray, P. F., &amp; Arnoult, C. (2020). Paternal epigenetics: Mammalian sperm provide much more than DNA at fertilization. Molecular and Cellular Endocrinology, 518, 110964. <a href=\"https:\/\/doi.org\/10.1016\/j.mce.2020.110964\">https:\/\/doi.org\/10.1016\/j.mce.2020.110964<\/a><\/p>\n\n\n\n<p>\u0141oboda, A., &amp; Dulak, J. (2020). Muscle and cardiac therapeutic strategies for Duchenne muscular dystrophy: Past, present, and future. Pharmacological Reports, 72(5), 1227\u20131263. <a href=\"https:\/\/doi.org\/10.1007\/s43440-020-00134-x\">https:\/\/doi.org\/10.1007\/s43440-020-00134-x<\/a><\/p>\n\n\n\n<p>Moia, R., Boggione, P., Mahmoud, A. M., Kodipad, A. A., Adhinaveni, R., Sagiraju, S., Patriarca, A., &amp; Gaidano, G. (2020). Targeting p53 in chronic lymphocytic leukemia. Expert Opinion on Therapeutic Targets, 24(12), 1239\u20131250. <a href=\"https:\/\/doi.org\/10.1080\/14728222.2020.1832465\">https:\/\/doi.org\/10.1080\/14728222.2020.1832465<\/a><\/p>\n\n\n\n<p>Park, J., Lee, K., Kim, K., &amp; Yi, S.-J. (2022). The role of histone modifications: From neurodevelopment to neurodiseases. Signal Transduction and Targeted Therapy, 7(1), 1\u201323. <a href=\"https:\/\/doi.org\/10.1038\/s41392-022-01078-9\">https:\/\/doi.org\/10.1038\/s41392-022-01078-9<\/a><\/p>\n\n\n\n<p>Pavan, A. R., Lopes, J. R., &amp; Dos Santos, J. L. (2022). The state of the art of fetal hemoglobin-inducing agents. Expert Opinion on Drug Discovery, 17(11), 1279\u20131293. <a href=\"https:\/\/doi.org\/10.1080\/17460441.2022.2141708\">https:\/\/doi.org\/10.1080\/17460441.2022.2141708<\/a><\/p>\n\n\n\n<p>Rogalska, M. E., Vivori, C., &amp; Valc\u00e1rcel, J. (2023). Regulation of pre-mRNA splicing: Roles in physiology and disease, and therapeutic prospects. Nature Reviews Genetics, 24(4), 251\u2013269. <a href=\"https:\/\/doi.org\/10.1038\/s41576-022-00556-8\">https:\/\/doi.org\/10.1038\/s41576-022-00556-8<\/a><\/p>\n\n\n\n<p>Shamshirgaran, Y., Liu, J., Sumer, H., Verma, P. J., &amp; Taheri-Ghahfarokhi, A. (2022). Tools for Efficient Genome Editing; ZFN, TALEN, and CRISPR. Methods in Molecular Biology (Clifton, N.J.), 2495, 29\u201346. <a href=\"https:\/\/doi.org\/10.1007\/978-1-0716-2301-5_2\">https:\/\/doi.org\/10.1007\/978-1-0716-2301-5_2<\/a><\/p>\n\n\n\n<p>Wang, Z. A., &amp; Cole, P. A. (2020). The Chemical Biology of Reversible Lysine Post-translational Modifications. Cell Chemical Biology, 27(8), 953\u2013969. <a href=\"https:\/\/doi.org\/10.1016\/j.chembiol.2020.07.002\">https:\/\/doi.org\/10.1016\/j.chembiol.2020.07.002<\/a><\/p>\n<\/details>\n<\/div>\n\n\n\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\" style=\"flex-basis:30%\">\n<div class=\"wp-block-group has-global-padding is-layout-constrained wp-block-group-is-layout-constrained wp-container-1 is-position-sticky\">\n<p class=\"has-small-font-size\" style=\"padding-top:var(--wp--preset--spacing--40);padding-bottom:0\"><strong>On this page<\/strong><\/p>\n\n\n\n<div class=\"wp-block-group is-vertical is-layout-flex wp-container-core-group-is-layout-fe9cc265 wp-block-group-is-layout-flex\"><div class=\"wp-block-aioseo-table-of-contents\"><ul><li><a class=\"aioseo-toc-item\" href=\"#aioseo-multiple-choice-questions\">Multiple-choice questions<\/a><\/li><li><a class=\"aioseo-toc-item\" href=\"#aioseo-questions-for-discussion\">Questions for Discussion<\/a><\/li><li><a class=\"aioseo-toc-item\" href=\"#aioseo-further-reading\">Further Reading<\/a><\/li><\/ul><\/div><\/div>\n<\/div>\n<\/div>\n<\/div>\n","protected":false},"featured_media":0,"parent":21,"menu_order":0,"template":"single-chapter","format":"standard","meta":{"_acf_changed":false},"class_list":["post-99","content","type-content","status-publish","format-standard","hentry"],"acf":[],"aioseo_notices":[],"_links":{"self":[{"href":"https:\/\/staging.routledgelearning.com\/genecontrol\/wp-json\/wp\/v2\/content\/99","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/staging.routledgelearning.com\/genecontrol\/wp-json\/wp\/v2\/content"}],"about":[{"href":"https:\/\/staging.routledgelearning.com\/genecontrol\/wp-json\/wp\/v2\/types\/content"}],"up":[{"embeddable":true,"href":"https:\/\/staging.routledgelearning.com\/genecontrol\/wp-json\/wp\/v2\/content\/21"}],"wp:attachment":[{"href":"https:\/\/staging.routledgelearning.com\/genecontrol\/wp-json\/wp\/v2\/media?parent=99"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}