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Human evolved regulatory elements modulate genes involved in cortical expansion and neurodevelopmental disease susceptibility
Modern genetic studies indicate that human brain evolution is driven primarily by changes in gene regulation, which requires understanding the biological function of largely non-coding gene regulatory elements, many of which act in tissue specific manner. We leverage chromatin interaction profiles i...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6546784/ https://www.ncbi.nlm.nih.gov/pubmed/31160561 http://dx.doi.org/10.1038/s41467-019-10248-3 |
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author | Won, Hyejung Huang, Jerry Opland, Carli K. Hartl, Chris L. Geschwind, Daniel H. |
author_facet | Won, Hyejung Huang, Jerry Opland, Carli K. Hartl, Chris L. Geschwind, Daniel H. |
author_sort | Won, Hyejung |
collection | PubMed |
description | Modern genetic studies indicate that human brain evolution is driven primarily by changes in gene regulation, which requires understanding the biological function of largely non-coding gene regulatory elements, many of which act in tissue specific manner. We leverage chromatin interaction profiles in human fetal and adult cortex to assign three classes of human-evolved elements to putative target genes. We find that human-evolved elements involving DNA sequence changes and those involving epigenetic changes are associated with human-specific gene regulation via effects on different classes of genes representing distinct biological pathways. However, both types of human-evolved elements converge on specific cell types and laminae involved in cerebral cortical expansion. Moreover, human evolved elements interact with neurodevelopmental disease risk genes, and genes with a high level of evolutionary constraint, highlighting a relationship between brain evolution and vulnerability to disorders affecting cognition and behavior. These results provide novel insights into gene regulatory mechanisms driving the evolution of human cognition and mechanisms of vulnerability to neuropsychiatric conditions. |
format | Online Article Text |
id | pubmed-6546784 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65467842019-06-18 Human evolved regulatory elements modulate genes involved in cortical expansion and neurodevelopmental disease susceptibility Won, Hyejung Huang, Jerry Opland, Carli K. Hartl, Chris L. Geschwind, Daniel H. Nat Commun Article Modern genetic studies indicate that human brain evolution is driven primarily by changes in gene regulation, which requires understanding the biological function of largely non-coding gene regulatory elements, many of which act in tissue specific manner. We leverage chromatin interaction profiles in human fetal and adult cortex to assign three classes of human-evolved elements to putative target genes. We find that human-evolved elements involving DNA sequence changes and those involving epigenetic changes are associated with human-specific gene regulation via effects on different classes of genes representing distinct biological pathways. However, both types of human-evolved elements converge on specific cell types and laminae involved in cerebral cortical expansion. Moreover, human evolved elements interact with neurodevelopmental disease risk genes, and genes with a high level of evolutionary constraint, highlighting a relationship between brain evolution and vulnerability to disorders affecting cognition and behavior. These results provide novel insights into gene regulatory mechanisms driving the evolution of human cognition and mechanisms of vulnerability to neuropsychiatric conditions. Nature Publishing Group UK 2019-06-03 /pmc/articles/PMC6546784/ /pubmed/31160561 http://dx.doi.org/10.1038/s41467-019-10248-3 Text en © The Author(s) 2019 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 Won, Hyejung Huang, Jerry Opland, Carli K. Hartl, Chris L. Geschwind, Daniel H. Human evolved regulatory elements modulate genes involved in cortical expansion and neurodevelopmental disease susceptibility |
title | Human evolved regulatory elements modulate genes involved in cortical expansion and neurodevelopmental disease susceptibility |
title_full | Human evolved regulatory elements modulate genes involved in cortical expansion and neurodevelopmental disease susceptibility |
title_fullStr | Human evolved regulatory elements modulate genes involved in cortical expansion and neurodevelopmental disease susceptibility |
title_full_unstemmed | Human evolved regulatory elements modulate genes involved in cortical expansion and neurodevelopmental disease susceptibility |
title_short | Human evolved regulatory elements modulate genes involved in cortical expansion and neurodevelopmental disease susceptibility |
title_sort | human evolved regulatory elements modulate genes involved in cortical expansion and neurodevelopmental disease susceptibility |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6546784/ https://www.ncbi.nlm.nih.gov/pubmed/31160561 http://dx.doi.org/10.1038/s41467-019-10248-3 |
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