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Selection on the regulation of sympathetic nervous activity in humans and chimpanzees
Adrenergic α(2)C receptor (ADRA2C) is an inhibitory modulator of the sympathetic nervous system. Knockout mice for this gene show physiological and behavioural alterations that are associated with the fight-or-flight response. There is evidence of positive selection on the regulation of this gene du...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5908061/ https://www.ncbi.nlm.nih.gov/pubmed/29672586 http://dx.doi.org/10.1371/journal.pgen.1007311 |
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author | Lee, Kang Seon Chatterjee, Paramita Choi, Eun-Young Sung, Min Kyung Oh, Jaeho Won, Hyejung Park, Seong-Min Kim, Youn-Jae Yi, Soojin V. Choi, Jung Kyoon |
author_facet | Lee, Kang Seon Chatterjee, Paramita Choi, Eun-Young Sung, Min Kyung Oh, Jaeho Won, Hyejung Park, Seong-Min Kim, Youn-Jae Yi, Soojin V. Choi, Jung Kyoon |
author_sort | Lee, Kang Seon |
collection | PubMed |
description | Adrenergic α(2)C receptor (ADRA2C) is an inhibitory modulator of the sympathetic nervous system. Knockout mice for this gene show physiological and behavioural alterations that are associated with the fight-or-flight response. There is evidence of positive selection on the regulation of this gene during chicken domestication. Here, we find that the neuronal expression of ADRA2C is lower in human and chimpanzee than in other primates. On the basis of three-dimensional chromatin structure, we identified a cis-regulatory region whose DNA sequences have been significantly accelerated in human and chimpanzee. Active histone modification marks this region in rhesus macaque but not in human and chimpanzee; instead, repressive marks are enriched in various human brain samples. This region contains two neuron-restrictive silencer factor (NRSF) binding motifs, each of which harbours a polymorphism. Our genotyping and analysis of population genome data indicate that at both polymorphic sites, the derived allele has reached fixation in humans and chimpanzees but not in bonobos, whereas only the ancestral allele is present among macaques. Our CRISPR/Cas9 genome editing and reporter assays show that both derived nucleotides repress ADRA2C, most likely by increasing NRSF binding. In addition, we detected signatures of recent positive selection for lower neuronal ADRA2C expression in humans. Our findings indicate that there has been selective pressure for enhanced sympathetic nervous activity in the evolution of humans and chimpanzees. |
format | Online Article Text |
id | pubmed-5908061 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-59080612018-05-06 Selection on the regulation of sympathetic nervous activity in humans and chimpanzees Lee, Kang Seon Chatterjee, Paramita Choi, Eun-Young Sung, Min Kyung Oh, Jaeho Won, Hyejung Park, Seong-Min Kim, Youn-Jae Yi, Soojin V. Choi, Jung Kyoon PLoS Genet Research Article Adrenergic α(2)C receptor (ADRA2C) is an inhibitory modulator of the sympathetic nervous system. Knockout mice for this gene show physiological and behavioural alterations that are associated with the fight-or-flight response. There is evidence of positive selection on the regulation of this gene during chicken domestication. Here, we find that the neuronal expression of ADRA2C is lower in human and chimpanzee than in other primates. On the basis of three-dimensional chromatin structure, we identified a cis-regulatory region whose DNA sequences have been significantly accelerated in human and chimpanzee. Active histone modification marks this region in rhesus macaque but not in human and chimpanzee; instead, repressive marks are enriched in various human brain samples. This region contains two neuron-restrictive silencer factor (NRSF) binding motifs, each of which harbours a polymorphism. Our genotyping and analysis of population genome data indicate that at both polymorphic sites, the derived allele has reached fixation in humans and chimpanzees but not in bonobos, whereas only the ancestral allele is present among macaques. Our CRISPR/Cas9 genome editing and reporter assays show that both derived nucleotides repress ADRA2C, most likely by increasing NRSF binding. In addition, we detected signatures of recent positive selection for lower neuronal ADRA2C expression in humans. Our findings indicate that there has been selective pressure for enhanced sympathetic nervous activity in the evolution of humans and chimpanzees. Public Library of Science 2018-04-19 /pmc/articles/PMC5908061/ /pubmed/29672586 http://dx.doi.org/10.1371/journal.pgen.1007311 Text en © 2018 Lee et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Lee, Kang Seon Chatterjee, Paramita Choi, Eun-Young Sung, Min Kyung Oh, Jaeho Won, Hyejung Park, Seong-Min Kim, Youn-Jae Yi, Soojin V. Choi, Jung Kyoon Selection on the regulation of sympathetic nervous activity in humans and chimpanzees |
title | Selection on the regulation of sympathetic nervous activity in humans and chimpanzees |
title_full | Selection on the regulation of sympathetic nervous activity in humans and chimpanzees |
title_fullStr | Selection on the regulation of sympathetic nervous activity in humans and chimpanzees |
title_full_unstemmed | Selection on the regulation of sympathetic nervous activity in humans and chimpanzees |
title_short | Selection on the regulation of sympathetic nervous activity in humans and chimpanzees |
title_sort | selection on the regulation of sympathetic nervous activity in humans and chimpanzees |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5908061/ https://www.ncbi.nlm.nih.gov/pubmed/29672586 http://dx.doi.org/10.1371/journal.pgen.1007311 |
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