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Hominin-specific regulatory elements selectively emerged in oligodendrocytes and are disrupted in autism patients
Speciation is associated with substantial rewiring of the regulatory circuitry underlying the expression of genes. Determining which changes are relevant and underlie the emergence of the human brain or its unique susceptibility to neural disease has been challenging. Here we annotate changes to gen...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6965079/ https://www.ncbi.nlm.nih.gov/pubmed/31949148 http://dx.doi.org/10.1038/s41467-019-14269-w |
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author | Castelijns, Bas Baak, Mirna L. Timpanaro, Ilia S. Wiggers, Caroline R. M. Vermunt, Marit W. Shang, Peng Kondova, Ivanela Geeven, Geert Bianchi, Valerio de Laat, Wouter Geijsen, Niels Creyghton, Menno P. |
author_facet | Castelijns, Bas Baak, Mirna L. Timpanaro, Ilia S. Wiggers, Caroline R. M. Vermunt, Marit W. Shang, Peng Kondova, Ivanela Geeven, Geert Bianchi, Valerio de Laat, Wouter Geijsen, Niels Creyghton, Menno P. |
author_sort | Castelijns, Bas |
collection | PubMed |
description | Speciation is associated with substantial rewiring of the regulatory circuitry underlying the expression of genes. Determining which changes are relevant and underlie the emergence of the human brain or its unique susceptibility to neural disease has been challenging. Here we annotate changes to gene regulatory elements (GREs) at cell type resolution in the brains of multiple primate species spanning most of primate evolution. We identify a unique set of regulatory elements that emerged in hominins prior to the separation of humans and chimpanzees. We demonstrate that these hominin gains perferentially affect oligodendrocyte function postnatally and are preferentially affected in the brains of autism patients. This preference is also observed for human-specific GREs suggesting this system is under continued selective pressure. Our data provide a roadmap of regulatory rewiring across primate evolution providing insight into the genomic changes that underlie the emergence of the brain and its susceptibility to neural disease. |
format | Online Article Text |
id | pubmed-6965079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69650792020-01-22 Hominin-specific regulatory elements selectively emerged in oligodendrocytes and are disrupted in autism patients Castelijns, Bas Baak, Mirna L. Timpanaro, Ilia S. Wiggers, Caroline R. M. Vermunt, Marit W. Shang, Peng Kondova, Ivanela Geeven, Geert Bianchi, Valerio de Laat, Wouter Geijsen, Niels Creyghton, Menno P. Nat Commun Article Speciation is associated with substantial rewiring of the regulatory circuitry underlying the expression of genes. Determining which changes are relevant and underlie the emergence of the human brain or its unique susceptibility to neural disease has been challenging. Here we annotate changes to gene regulatory elements (GREs) at cell type resolution in the brains of multiple primate species spanning most of primate evolution. We identify a unique set of regulatory elements that emerged in hominins prior to the separation of humans and chimpanzees. We demonstrate that these hominin gains perferentially affect oligodendrocyte function postnatally and are preferentially affected in the brains of autism patients. This preference is also observed for human-specific GREs suggesting this system is under continued selective pressure. Our data provide a roadmap of regulatory rewiring across primate evolution providing insight into the genomic changes that underlie the emergence of the brain and its susceptibility to neural disease. Nature Publishing Group UK 2020-01-16 /pmc/articles/PMC6965079/ /pubmed/31949148 http://dx.doi.org/10.1038/s41467-019-14269-w Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Castelijns, Bas Baak, Mirna L. Timpanaro, Ilia S. Wiggers, Caroline R. M. Vermunt, Marit W. Shang, Peng Kondova, Ivanela Geeven, Geert Bianchi, Valerio de Laat, Wouter Geijsen, Niels Creyghton, Menno P. Hominin-specific regulatory elements selectively emerged in oligodendrocytes and are disrupted in autism patients |
title | Hominin-specific regulatory elements selectively emerged in oligodendrocytes and are disrupted in autism patients |
title_full | Hominin-specific regulatory elements selectively emerged in oligodendrocytes and are disrupted in autism patients |
title_fullStr | Hominin-specific regulatory elements selectively emerged in oligodendrocytes and are disrupted in autism patients |
title_full_unstemmed | Hominin-specific regulatory elements selectively emerged in oligodendrocytes and are disrupted in autism patients |
title_short | Hominin-specific regulatory elements selectively emerged in oligodendrocytes and are disrupted in autism patients |
title_sort | hominin-specific regulatory elements selectively emerged in oligodendrocytes and are disrupted in autism patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6965079/ https://www.ncbi.nlm.nih.gov/pubmed/31949148 http://dx.doi.org/10.1038/s41467-019-14269-w |
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