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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.
Afiliação
  • Ang CE; Department of Pathology, Institute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, United States.
  • Ma Q; Department of Bioengineering, Stanford University, Stanford, United States.
  • Wapinski OL; Center for Personal Dynamic Regulomes, Stanford University, Stanford, United States.
  • Fan S; Department of Dermatology, Stanford University, Stanford, United States.
  • Flynn RA; Department of Genetics, Stanford University, Stanford, United States.
  • Lee QY; Center for Personal Dynamic Regulomes, Stanford University, Stanford, United States.
  • Coe B; Department of Dermatology, Stanford University, Stanford, United States.
  • Onoguchi M; Department of Genetics, Stanford University, Stanford, United States.
  • Olmos VH; JC Self Research Institute of Human Genetics, Greenwood Genetic Center, Greenwood, United States.
  • Do BT; Center for Personal Dynamic Regulomes, Stanford University, Stanford, United States.
  • Dukes-Rimsky L; Department of Dermatology, Stanford University, Stanford, United States.
  • Xu J; Department of Genetics, Stanford University, Stanford, United States.
  • Tanabe K; Department of Pathology, Institute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, United States.
  • Wang L; Department of Bioengineering, Stanford University, Stanford, United States.
  • Elling U; Department of Genome Sciences, Howard Hughes Medical Institute, University of Washington, Seattle, United States.
  • Penninger JM; Center for Personal Dynamic Regulomes, Stanford University, Stanford, United States.
  • Zhao Y; Department of Dermatology, Stanford University, Stanford, United States.
  • Qu K; Department of Genetics, Stanford University, Stanford, United States.
  • Eichler EE; Department of Pathology, Institute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, United States.
  • Srivastava A; Center for Personal Dynamic Regulomes, Stanford University, Stanford, United States.
  • Wernig M; JC Self Research Institute of Human Genetics, Greenwood Genetic Center, Greenwood, United States.
  • Chang HY; Center for Personal Dynamic Regulomes, Stanford University, Stanford, United States.
Elife ; 82019 01 10.
Article em En | MEDLINE | ID: mdl-30628890
ABSTRACT
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(512) 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diferenciação Celular / RNA Longo não Codificante / Transtornos do Neurodesenvolvimento / Transtorno do Espectro Autista / Mutação / Neurônios Limite: Child / Female / Humans / Male Idioma: En Revista: Elife Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diferenciação Celular / RNA Longo não Codificante / Transtornos do Neurodesenvolvimento / Transtorno do Espectro Autista / Mutação / Neurônios Limite: Child / Female / Humans / Male Idioma: En Revista: Elife Ano de publicação: 2019 Tipo de documento: Article