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Weak gene–gene interaction facilitates the evolution of gene expression plasticity

BACKGROUND: Individual organisms may exhibit phenotypic plasticity when they acclimate to different conditions. Such plastic responses may facilitate or constrain the adaptation of their descendant populations to new environments, complicating their evolutionary trajectories beyond the genetic bluep...

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Autores principales: Kuo, Hao-Chih, Yao, Cheng-Te, Liao, Ben-Yang, Weng, Meng-Pin, Dong, Feng, Hsu, Yu-Cheng, Hung, Chih-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10029303/
https://www.ncbi.nlm.nih.gov/pubmed/36941675
http://dx.doi.org/10.1186/s12915-023-01558-6
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author Kuo, Hao-Chih
Yao, Cheng-Te
Liao, Ben-Yang
Weng, Meng-Pin
Dong, Feng
Hsu, Yu-Cheng
Hung, Chih-Ming
author_facet Kuo, Hao-Chih
Yao, Cheng-Te
Liao, Ben-Yang
Weng, Meng-Pin
Dong, Feng
Hsu, Yu-Cheng
Hung, Chih-Ming
author_sort Kuo, Hao-Chih
collection PubMed
description BACKGROUND: Individual organisms may exhibit phenotypic plasticity when they acclimate to different conditions. Such plastic responses may facilitate or constrain the adaptation of their descendant populations to new environments, complicating their evolutionary trajectories beyond the genetic blueprint. Intriguingly, phenotypic plasticity itself can evolve in terms of its direction and magnitude during adaptation. However, we know little about what determines the evolution of phenotypic plasticity, including gene expression plasticity. Recent laboratory-based studies suggest dominance of reversing gene expression plasticity—plastic responses that move the levels of gene expression away from the new optima. Nevertheless, evidence from natural populations is still limited. RESULTS: Here, we studied gene expression plasticity and its evolution in the montane and lowland populations of an elevationally widespread songbird—the Rufous-capped Babbler (Cyanoderma ruficeps)—with reciprocal transplant experiments and transcriptomic analyses; we set common gardens at altitudes close to these populations’ native ranges. We confirmed the prevalence of reversing plasticity in genes associated with altitudinal adaptation. Interestingly, we found a positive relationship between magnitude and degree of evolution in gene expression plasticity, which was pertinent to not only adaptation-associated genes but also the whole transcriptomes from multiple tissues. Furthermore, we revealed that genes with weaker expressional interactions with other genes tended to exhibit stronger plasticity and higher degree of plasticity evolution, which explains the positive magnitude-evolution relationship. CONCLUSIONS: Our experimental evidence demonstrates that species may initiate their adaptation to new habitats with genes exhibiting strong expression plasticity. We also highlight the role of expression interdependence among genes in regulating the magnitude and evolution of expression plasticity. This study illuminates how the evolution of phenotypic plasticity in gene expression facilitates the adaptation of species to challenging environments in nature. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-023-01558-6.
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spelling pubmed-100293032023-03-22 Weak gene–gene interaction facilitates the evolution of gene expression plasticity Kuo, Hao-Chih Yao, Cheng-Te Liao, Ben-Yang Weng, Meng-Pin Dong, Feng Hsu, Yu-Cheng Hung, Chih-Ming BMC Biol Research Article BACKGROUND: Individual organisms may exhibit phenotypic plasticity when they acclimate to different conditions. Such plastic responses may facilitate or constrain the adaptation of their descendant populations to new environments, complicating their evolutionary trajectories beyond the genetic blueprint. Intriguingly, phenotypic plasticity itself can evolve in terms of its direction and magnitude during adaptation. However, we know little about what determines the evolution of phenotypic plasticity, including gene expression plasticity. Recent laboratory-based studies suggest dominance of reversing gene expression plasticity—plastic responses that move the levels of gene expression away from the new optima. Nevertheless, evidence from natural populations is still limited. RESULTS: Here, we studied gene expression plasticity and its evolution in the montane and lowland populations of an elevationally widespread songbird—the Rufous-capped Babbler (Cyanoderma ruficeps)—with reciprocal transplant experiments and transcriptomic analyses; we set common gardens at altitudes close to these populations’ native ranges. We confirmed the prevalence of reversing plasticity in genes associated with altitudinal adaptation. Interestingly, we found a positive relationship between magnitude and degree of evolution in gene expression plasticity, which was pertinent to not only adaptation-associated genes but also the whole transcriptomes from multiple tissues. Furthermore, we revealed that genes with weaker expressional interactions with other genes tended to exhibit stronger plasticity and higher degree of plasticity evolution, which explains the positive magnitude-evolution relationship. CONCLUSIONS: Our experimental evidence demonstrates that species may initiate their adaptation to new habitats with genes exhibiting strong expression plasticity. We also highlight the role of expression interdependence among genes in regulating the magnitude and evolution of expression plasticity. This study illuminates how the evolution of phenotypic plasticity in gene expression facilitates the adaptation of species to challenging environments in nature. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-023-01558-6. BioMed Central 2023-03-20 /pmc/articles/PMC10029303/ /pubmed/36941675 http://dx.doi.org/10.1186/s12915-023-01558-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Kuo, Hao-Chih
Yao, Cheng-Te
Liao, Ben-Yang
Weng, Meng-Pin
Dong, Feng
Hsu, Yu-Cheng
Hung, Chih-Ming
Weak gene–gene interaction facilitates the evolution of gene expression plasticity
title Weak gene–gene interaction facilitates the evolution of gene expression plasticity
title_full Weak gene–gene interaction facilitates the evolution of gene expression plasticity
title_fullStr Weak gene–gene interaction facilitates the evolution of gene expression plasticity
title_full_unstemmed Weak gene–gene interaction facilitates the evolution of gene expression plasticity
title_short Weak gene–gene interaction facilitates the evolution of gene expression plasticity
title_sort weak gene–gene interaction facilitates the evolution of gene expression plasticity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10029303/
https://www.ncbi.nlm.nih.gov/pubmed/36941675
http://dx.doi.org/10.1186/s12915-023-01558-6
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