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Genome architecture and selective signals compensatorily shape plastic response to a new environment
Transcriptional plasticity interacts with natural selection in complex ways and is crucial for the survival of species under rapid climate change. How 3D genome architecture affects transcriptional plasticity and its interaction with genetic adaptation are unclear. We transplanted estuarine oysters...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10362523/ https://www.ncbi.nlm.nih.gov/pubmed/37485076 http://dx.doi.org/10.1016/j.xinn.2023.100464 |
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author | Li, Ao Zhao, Mingjie Zhang, Ziyan Wang, Chaogang Zhang, Kexin Zhang, Xu De Wit, Pierre Raoul Wang, Wei Gao, Juntao Guo, Ximing Zhang, Guofan Li, Li |
author_facet | Li, Ao Zhao, Mingjie Zhang, Ziyan Wang, Chaogang Zhang, Kexin Zhang, Xu De Wit, Pierre Raoul Wang, Wei Gao, Juntao Guo, Ximing Zhang, Guofan Li, Li |
author_sort | Li, Ao |
collection | PubMed |
description | Transcriptional plasticity interacts with natural selection in complex ways and is crucial for the survival of species under rapid climate change. How 3D genome architecture affects transcriptional plasticity and its interaction with genetic adaptation are unclear. We transplanted estuarine oysters to a new environment and found that genes located in active chromatin regions exhibited greater transcriptional plasticity, and changes in these regions were negatively correlated with selective signals. This indicates a trade-off between 3D active regions and selective signals in shaping plastic responses to a new environment. Specifically, a mutation, lincRNA, and changes in the accessibility of a distal enhancer potentially affect its interaction with the ManⅡa gene, which regulates the muscle function and survival of oysters. Our findings reveal that 3D genome architecture compensates for the role of genetic adaptation in environmental response to new environments and provide insights into synergetic genetic and epigenetic interactions critical for fitness-related trait and survival in a model marine species. |
format | Online Article Text |
id | pubmed-10362523 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-103625232023-07-23 Genome architecture and selective signals compensatorily shape plastic response to a new environment Li, Ao Zhao, Mingjie Zhang, Ziyan Wang, Chaogang Zhang, Kexin Zhang, Xu De Wit, Pierre Raoul Wang, Wei Gao, Juntao Guo, Ximing Zhang, Guofan Li, Li Innovation (Camb) Article Transcriptional plasticity interacts with natural selection in complex ways and is crucial for the survival of species under rapid climate change. How 3D genome architecture affects transcriptional plasticity and its interaction with genetic adaptation are unclear. We transplanted estuarine oysters to a new environment and found that genes located in active chromatin regions exhibited greater transcriptional plasticity, and changes in these regions were negatively correlated with selective signals. This indicates a trade-off between 3D active regions and selective signals in shaping plastic responses to a new environment. Specifically, a mutation, lincRNA, and changes in the accessibility of a distal enhancer potentially affect its interaction with the ManⅡa gene, which regulates the muscle function and survival of oysters. Our findings reveal that 3D genome architecture compensates for the role of genetic adaptation in environmental response to new environments and provide insights into synergetic genetic and epigenetic interactions critical for fitness-related trait and survival in a model marine species. Elsevier 2023-06-21 /pmc/articles/PMC10362523/ /pubmed/37485076 http://dx.doi.org/10.1016/j.xinn.2023.100464 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Li, Ao Zhao, Mingjie Zhang, Ziyan Wang, Chaogang Zhang, Kexin Zhang, Xu De Wit, Pierre Raoul Wang, Wei Gao, Juntao Guo, Ximing Zhang, Guofan Li, Li Genome architecture and selective signals compensatorily shape plastic response to a new environment |
title | Genome architecture and selective signals compensatorily shape plastic response to a new environment |
title_full | Genome architecture and selective signals compensatorily shape plastic response to a new environment |
title_fullStr | Genome architecture and selective signals compensatorily shape plastic response to a new environment |
title_full_unstemmed | Genome architecture and selective signals compensatorily shape plastic response to a new environment |
title_short | Genome architecture and selective signals compensatorily shape plastic response to a new environment |
title_sort | genome architecture and selective signals compensatorily shape plastic response to a new environment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10362523/ https://www.ncbi.nlm.nih.gov/pubmed/37485076 http://dx.doi.org/10.1016/j.xinn.2023.100464 |
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