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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...

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Autores principales: Uebbing, Severin, Gockley, Jake, Reilly, Steven K., Kocher, Acadia A., Geller, Evan, Gandotra, Neeru, Scharfe, Curt, Cotney, Justin, Noonan, James P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2021
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.
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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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