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Massively parallel discovery of human-specific substitutions that alter enhancer activity
Genetic changes that altered the function of gene regulatory elements have been implicated in the evolution of human traits such as the expansion of the cerebral cortex. However, identifying the particular changes that modified regulatory activity during human evolution remain challenging. Here we u...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7812811/ https://www.ncbi.nlm.nih.gov/pubmed/33372131 http://dx.doi.org/10.1073/pnas.2007049118 |
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author | Uebbing, Severin Gockley, Jake Reilly, Steven K. Kocher, Acadia A. Geller, Evan Gandotra, Neeru Scharfe, Curt Cotney, Justin Noonan, James P. |
author_facet | Uebbing, Severin Gockley, Jake Reilly, Steven K. Kocher, Acadia A. Geller, Evan Gandotra, Neeru Scharfe, Curt Cotney, Justin Noonan, James P. |
author_sort | Uebbing, Severin |
collection | PubMed |
description | Genetic changes that altered the function of gene regulatory elements have been implicated in the evolution of human traits such as the expansion of the cerebral cortex. However, identifying the particular changes that modified regulatory activity during human evolution remain challenging. Here we used massively parallel enhancer assays in neural stem cells to quantify the functional impact of >32,000 human-specific substitutions in >4,300 human accelerated regions (HARs) and human gain enhancers (HGEs), which include enhancers with novel activities in humans. We found that >30% of active HARs and HGEs exhibited differential activity between human and chimpanzee. We isolated the effects of human-specific substitutions from background genetic variation to identify the effects of genetic changes most relevant to human evolution. We found that substitutions interacted in both additive and nonadditive ways to modify enhancer function. Substitutions within HARs, which are highly constrained compared to HGEs, showed smaller effects on enhancer activity, suggesting that the impact of human-specific substitutions is buffered in enhancers with constrained ancestral functions. Our findings yield insight into how human-specific genetic changes altered enhancer function and provide a rich set of candidates for studies of regulatory evolution in humans. |
format | Online Article Text |
id | pubmed-7812811 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-78128112021-01-28 Massively parallel discovery of human-specific substitutions that alter enhancer activity Uebbing, Severin Gockley, Jake Reilly, Steven K. Kocher, Acadia A. Geller, Evan Gandotra, Neeru Scharfe, Curt Cotney, Justin Noonan, James P. Proc Natl Acad Sci U S A Biological Sciences Genetic changes that altered the function of gene regulatory elements have been implicated in the evolution of human traits such as the expansion of the cerebral cortex. However, identifying the particular changes that modified regulatory activity during human evolution remain challenging. Here we used massively parallel enhancer assays in neural stem cells to quantify the functional impact of >32,000 human-specific substitutions in >4,300 human accelerated regions (HARs) and human gain enhancers (HGEs), which include enhancers with novel activities in humans. We found that >30% of active HARs and HGEs exhibited differential activity between human and chimpanzee. We isolated the effects of human-specific substitutions from background genetic variation to identify the effects of genetic changes most relevant to human evolution. We found that substitutions interacted in both additive and nonadditive ways to modify enhancer function. Substitutions within HARs, which are highly constrained compared to HGEs, showed smaller effects on enhancer activity, suggesting that the impact of human-specific substitutions is buffered in enhancers with constrained ancestral functions. Our findings yield insight into how human-specific genetic changes altered enhancer function and provide a rich set of candidates for studies of regulatory evolution in humans. National Academy of Sciences 2021-01-12 2020-12-28 /pmc/articles/PMC7812811/ /pubmed/33372131 http://dx.doi.org/10.1073/pnas.2007049118 Text en Copyright © 2020 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Uebbing, Severin Gockley, Jake Reilly, Steven K. Kocher, Acadia A. Geller, Evan Gandotra, Neeru Scharfe, Curt Cotney, Justin Noonan, James P. Massively parallel discovery of human-specific substitutions that alter enhancer activity |
title | Massively parallel discovery of human-specific substitutions that alter enhancer activity |
title_full | Massively parallel discovery of human-specific substitutions that alter enhancer activity |
title_fullStr | Massively parallel discovery of human-specific substitutions that alter enhancer activity |
title_full_unstemmed | Massively parallel discovery of human-specific substitutions that alter enhancer activity |
title_short | Massively parallel discovery of human-specific substitutions that alter enhancer activity |
title_sort | massively parallel discovery of human-specific substitutions that alter enhancer activity |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7812811/ https://www.ncbi.nlm.nih.gov/pubmed/33372131 http://dx.doi.org/10.1073/pnas.2007049118 |
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