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The novel lncRNA lnc-NR2F1 is pro-neurogenic and mutated in human neurodevelopmental disorders
Long noncoding RNAs (lncRNAs) have been shown to act as important cell biological regulators including cell fate decisions but are often ignored in human genetics. Combining differential lncRNA expression during neuronal lineage induction with copy number variation morbidity maps of a cohort of chil...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6380841/ https://www.ncbi.nlm.nih.gov/pubmed/30628890 http://dx.doi.org/10.7554/eLife.41770 |
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author | Ang, Cheen Euong Ma, Qing Wapinski, Orly L Fan, ShengHua Flynn, Ryan A Lee, Qian Yi Coe, Bradley Onoguchi, Masahiro Olmos, Victor Hipolito Do, Brian T Dukes-Rimsky, Lynn Xu, Jin Tanabe, Koji Wang, LiangJiang Elling, Ulrich Penninger, Josef M Zhao, Yang Qu, Kun Eichler, Evan E Srivastava, Anand Wernig, Marius Chang, Howard Y |
author_facet | Ang, Cheen Euong Ma, Qing Wapinski, Orly L Fan, ShengHua Flynn, Ryan A Lee, Qian Yi Coe, Bradley Onoguchi, Masahiro Olmos, Victor Hipolito Do, Brian T Dukes-Rimsky, Lynn Xu, Jin Tanabe, Koji Wang, LiangJiang Elling, Ulrich Penninger, Josef M Zhao, Yang Qu, Kun Eichler, Evan E Srivastava, Anand Wernig, Marius Chang, Howard Y |
author_sort | Ang, Cheen Euong |
collection | PubMed |
description | Long noncoding RNAs (lncRNAs) have been shown to act as important cell biological regulators including cell fate decisions but are often ignored in human genetics. Combining differential lncRNA expression during neuronal lineage induction with copy number variation morbidity maps of a cohort of children with autism spectrum disorder/intellectual disability versus healthy controls revealed focal genomic mutations affecting several lncRNA candidate loci. Here we find that a t(5:12) chromosomal translocation in a family manifesting neurodevelopmental symptoms disrupts specifically lnc-NR2F1. We further show that lnc-NR2F1 is an evolutionarily conserved lncRNA functionally enhances induced neuronal cell maturation and directly occupies and regulates transcription of neuronal genes including autism-associated genes. Thus, integrating human genetics and functional testing in neuronal lineage induction is a promising approach for discovering candidate lncRNAs involved in neurodevelopmental diseases. |
format | Online Article Text |
id | pubmed-6380841 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-63808412019-02-20 The novel lncRNA lnc-NR2F1 is pro-neurogenic and mutated in human neurodevelopmental disorders Ang, Cheen Euong Ma, Qing Wapinski, Orly L Fan, ShengHua Flynn, Ryan A Lee, Qian Yi Coe, Bradley Onoguchi, Masahiro Olmos, Victor Hipolito Do, Brian T Dukes-Rimsky, Lynn Xu, Jin Tanabe, Koji Wang, LiangJiang Elling, Ulrich Penninger, Josef M Zhao, Yang Qu, Kun Eichler, Evan E Srivastava, Anand Wernig, Marius Chang, Howard Y eLife Genetics and Genomics Long noncoding RNAs (lncRNAs) have been shown to act as important cell biological regulators including cell fate decisions but are often ignored in human genetics. Combining differential lncRNA expression during neuronal lineage induction with copy number variation morbidity maps of a cohort of children with autism spectrum disorder/intellectual disability versus healthy controls revealed focal genomic mutations affecting several lncRNA candidate loci. Here we find that a t(5:12) chromosomal translocation in a family manifesting neurodevelopmental symptoms disrupts specifically lnc-NR2F1. We further show that lnc-NR2F1 is an evolutionarily conserved lncRNA functionally enhances induced neuronal cell maturation and directly occupies and regulates transcription of neuronal genes including autism-associated genes. Thus, integrating human genetics and functional testing in neuronal lineage induction is a promising approach for discovering candidate lncRNAs involved in neurodevelopmental diseases. eLife Sciences Publications, Ltd 2019-01-10 /pmc/articles/PMC6380841/ /pubmed/30628890 http://dx.doi.org/10.7554/eLife.41770 Text en © 2019, Ang et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Genetics and Genomics Ang, Cheen Euong Ma, Qing Wapinski, Orly L Fan, ShengHua Flynn, Ryan A Lee, Qian Yi Coe, Bradley Onoguchi, Masahiro Olmos, Victor Hipolito Do, Brian T Dukes-Rimsky, Lynn Xu, Jin Tanabe, Koji Wang, LiangJiang Elling, Ulrich Penninger, Josef M Zhao, Yang Qu, Kun Eichler, Evan E Srivastava, Anand Wernig, Marius Chang, Howard Y The novel lncRNA lnc-NR2F1 is pro-neurogenic and mutated in human neurodevelopmental disorders |
title | The novel lncRNA lnc-NR2F1 is pro-neurogenic and mutated in human neurodevelopmental disorders |
title_full | The novel lncRNA lnc-NR2F1 is pro-neurogenic and mutated in human neurodevelopmental disorders |
title_fullStr | The novel lncRNA lnc-NR2F1 is pro-neurogenic and mutated in human neurodevelopmental disorders |
title_full_unstemmed | The novel lncRNA lnc-NR2F1 is pro-neurogenic and mutated in human neurodevelopmental disorders |
title_short | The novel lncRNA lnc-NR2F1 is pro-neurogenic and mutated in human neurodevelopmental disorders |
title_sort | novel lncrna lnc-nr2f1 is pro-neurogenic and mutated in human neurodevelopmental disorders |
topic | Genetics and Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6380841/ https://www.ncbi.nlm.nih.gov/pubmed/30628890 http://dx.doi.org/10.7554/eLife.41770 |
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