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Gene Duplication and Loss of AANAT in Mammals Driven by Rhythmic Adaptations
Arylalkylamine N-acetyltransferase (AANAT) plays a crucial role in synchronizing internal biological functions to circadian and circannual changes. Generally speaking, only one copy of AANAT gene has been found in mammals, however, three independent duplications of this gene were detected in several...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8382898/ https://www.ncbi.nlm.nih.gov/pubmed/33944919 http://dx.doi.org/10.1093/molbev/msab125 |
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author | Yin, Daiqing Zhou, RuRu Yin, Mengxin Chen, Yue Xu, Shixia Yang, Guang |
author_facet | Yin, Daiqing Zhou, RuRu Yin, Mengxin Chen, Yue Xu, Shixia Yang, Guang |
author_sort | Yin, Daiqing |
collection | PubMed |
description | Arylalkylamine N-acetyltransferase (AANAT) plays a crucial role in synchronizing internal biological functions to circadian and circannual changes. Generally speaking, only one copy of AANAT gene has been found in mammals, however, three independent duplications of this gene were detected in several cetartiodactyl lineages (i.e., Suidae, Hippopotamidae, and Pecora), which originated in the middle Eocene, a geological period characterized with the increased climate seasonality. Lineage-specific expansions of AANAT and the associated functional enhancement in these lineages strongly suggest an improvement in regulating photoperiodic response to adapt to seasonal climate changes. In contrast, independent inactivating mutations or deletions of the AANAT locus were identified in the four pineal-deficient clades (cetaceans, sirenians, xenarthrans, and pangolins). Loss of AANAT function in cetaceans and sirenians could disrupt the sleep-promoting effects of pineal melatonin, which might contribute to increasing wakefulness, adapting these clades to underwater sleep. The absence of AANAT and pineal glands in xenarthrans and pangolins may be associated with their body temperature maintenance. The present work demonstrates a far more complex and intriguing evolutionary pattern and functional diversity of mammalian AANAT genes than previously thought and provides further evidence for understanding AANAT evolution as driven by rhythmic adaptations in mammals. |
format | Online Article Text |
id | pubmed-8382898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-83828982021-08-25 Gene Duplication and Loss of AANAT in Mammals Driven by Rhythmic Adaptations Yin, Daiqing Zhou, RuRu Yin, Mengxin Chen, Yue Xu, Shixia Yang, Guang Mol Biol Evol Discoveries Arylalkylamine N-acetyltransferase (AANAT) plays a crucial role in synchronizing internal biological functions to circadian and circannual changes. Generally speaking, only one copy of AANAT gene has been found in mammals, however, three independent duplications of this gene were detected in several cetartiodactyl lineages (i.e., Suidae, Hippopotamidae, and Pecora), which originated in the middle Eocene, a geological period characterized with the increased climate seasonality. Lineage-specific expansions of AANAT and the associated functional enhancement in these lineages strongly suggest an improvement in regulating photoperiodic response to adapt to seasonal climate changes. In contrast, independent inactivating mutations or deletions of the AANAT locus were identified in the four pineal-deficient clades (cetaceans, sirenians, xenarthrans, and pangolins). Loss of AANAT function in cetaceans and sirenians could disrupt the sleep-promoting effects of pineal melatonin, which might contribute to increasing wakefulness, adapting these clades to underwater sleep. The absence of AANAT and pineal glands in xenarthrans and pangolins may be associated with their body temperature maintenance. The present work demonstrates a far more complex and intriguing evolutionary pattern and functional diversity of mammalian AANAT genes than previously thought and provides further evidence for understanding AANAT evolution as driven by rhythmic adaptations in mammals. Oxford University Press 2021-05-03 /pmc/articles/PMC8382898/ /pubmed/33944919 http://dx.doi.org/10.1093/molbev/msab125 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Discoveries Yin, Daiqing Zhou, RuRu Yin, Mengxin Chen, Yue Xu, Shixia Yang, Guang Gene Duplication and Loss of AANAT in Mammals Driven by Rhythmic Adaptations |
title | Gene Duplication and Loss of AANAT in Mammals Driven by Rhythmic Adaptations |
title_full | Gene Duplication and Loss of AANAT in Mammals Driven by Rhythmic Adaptations |
title_fullStr | Gene Duplication and Loss of AANAT in Mammals Driven by Rhythmic Adaptations |
title_full_unstemmed | Gene Duplication and Loss of AANAT in Mammals Driven by Rhythmic Adaptations |
title_short | Gene Duplication and Loss of AANAT in Mammals Driven by Rhythmic Adaptations |
title_sort | gene duplication and loss of aanat in mammals driven by rhythmic adaptations |
topic | Discoveries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8382898/ https://www.ncbi.nlm.nih.gov/pubmed/33944919 http://dx.doi.org/10.1093/molbev/msab125 |
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