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Genome of the estuarine oyster provides insights into climate impact and adaptive plasticity

Understanding the roles of genetic divergence and phenotypic plasticity in adaptation is central to evolutionary biology and important for assessing adaptive potential of species under climate change. Analysis of a chromosome-level assembly and resequencing of individuals across wide latitude distri...

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Autores principales: Li, Ao, Dai, He, Guo, Ximing, Zhang, Ziyan, Zhang, Kexin, Wang, Chaogang, Wang, Xinxing, Wang, Wei, Chen, Hongju, Li, Xumin, Zheng, Hongkun, Li, Li, Zhang, Guofan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8590024/
https://www.ncbi.nlm.nih.gov/pubmed/34773106
http://dx.doi.org/10.1038/s42003-021-02823-6
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author Li, Ao
Dai, He
Guo, Ximing
Zhang, Ziyan
Zhang, Kexin
Wang, Chaogang
Wang, Xinxing
Wang, Wei
Chen, Hongju
Li, Xumin
Zheng, Hongkun
Li, Li
Zhang, Guofan
author_facet Li, Ao
Dai, He
Guo, Ximing
Zhang, Ziyan
Zhang, Kexin
Wang, Chaogang
Wang, Xinxing
Wang, Wei
Chen, Hongju
Li, Xumin
Zheng, Hongkun
Li, Li
Zhang, Guofan
author_sort Li, Ao
collection PubMed
description Understanding the roles of genetic divergence and phenotypic plasticity in adaptation is central to evolutionary biology and important for assessing adaptive potential of species under climate change. Analysis of a chromosome-level assembly and resequencing of individuals across wide latitude distribution in the estuarine oyster (Crassostrea ariakensis) revealed unexpectedly low genomic diversity and population structures shaped by historical glaciation, geological events and oceanographic forces. Strong selection signals were detected in genes responding to temperature and salinity stress, especially of the expanded solute carrier families, highlighting the importance of gene expansion in environmental adaptation. Genes exhibiting high plasticity showed strong selection in upstream regulatory regions that modulate transcription, indicating selection favoring plasticity. Our findings suggest that genomic variation and population structure in marine bivalves are heavily influenced by climate history and physical forces, and gene expansion and selection may enhance phenotypic plasticity that is critical for the adaptation to rapidly changing environments.
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spelling pubmed-85900242021-11-15 Genome of the estuarine oyster provides insights into climate impact and adaptive plasticity Li, Ao Dai, He Guo, Ximing Zhang, Ziyan Zhang, Kexin Wang, Chaogang Wang, Xinxing Wang, Wei Chen, Hongju Li, Xumin Zheng, Hongkun Li, Li Zhang, Guofan Commun Biol Article Understanding the roles of genetic divergence and phenotypic plasticity in adaptation is central to evolutionary biology and important for assessing adaptive potential of species under climate change. Analysis of a chromosome-level assembly and resequencing of individuals across wide latitude distribution in the estuarine oyster (Crassostrea ariakensis) revealed unexpectedly low genomic diversity and population structures shaped by historical glaciation, geological events and oceanographic forces. Strong selection signals were detected in genes responding to temperature and salinity stress, especially of the expanded solute carrier families, highlighting the importance of gene expansion in environmental adaptation. Genes exhibiting high plasticity showed strong selection in upstream regulatory regions that modulate transcription, indicating selection favoring plasticity. Our findings suggest that genomic variation and population structure in marine bivalves are heavily influenced by climate history and physical forces, and gene expansion and selection may enhance phenotypic plasticity that is critical for the adaptation to rapidly changing environments. Nature Publishing Group UK 2021-11-12 /pmc/articles/PMC8590024/ /pubmed/34773106 http://dx.doi.org/10.1038/s42003-021-02823-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Li, Ao
Dai, He
Guo, Ximing
Zhang, Ziyan
Zhang, Kexin
Wang, Chaogang
Wang, Xinxing
Wang, Wei
Chen, Hongju
Li, Xumin
Zheng, Hongkun
Li, Li
Zhang, Guofan
Genome of the estuarine oyster provides insights into climate impact and adaptive plasticity
title Genome of the estuarine oyster provides insights into climate impact and adaptive plasticity
title_full Genome of the estuarine oyster provides insights into climate impact and adaptive plasticity
title_fullStr Genome of the estuarine oyster provides insights into climate impact and adaptive plasticity
title_full_unstemmed Genome of the estuarine oyster provides insights into climate impact and adaptive plasticity
title_short Genome of the estuarine oyster provides insights into climate impact and adaptive plasticity
title_sort genome of the estuarine oyster provides insights into climate impact and adaptive plasticity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8590024/
https://www.ncbi.nlm.nih.gov/pubmed/34773106
http://dx.doi.org/10.1038/s42003-021-02823-6
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