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Evolution of Spatial and Temporal cis-Regulatory Divergence in Sticklebacks

Cis-regulatory changes are thought to play a major role in adaptation. Threespine sticklebacks have repeatedly colonized freshwater habitats in the Northern Hemisphere, where they have evolved a suite of phenotypes that distinguish them from marine populations, including changes in physiology, behav...

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Autores principales: Mack, Katya L, Square, Tyler A, Zhao, Bin, Miller, Craig T, Fraser, Hunter B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10015619/
https://www.ncbi.nlm.nih.gov/pubmed/36805962
http://dx.doi.org/10.1093/molbev/msad034
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author Mack, Katya L
Square, Tyler A
Zhao, Bin
Miller, Craig T
Fraser, Hunter B
author_facet Mack, Katya L
Square, Tyler A
Zhao, Bin
Miller, Craig T
Fraser, Hunter B
author_sort Mack, Katya L
collection PubMed
description Cis-regulatory changes are thought to play a major role in adaptation. Threespine sticklebacks have repeatedly colonized freshwater habitats in the Northern Hemisphere, where they have evolved a suite of phenotypes that distinguish them from marine populations, including changes in physiology, behavior, and morphology. To understand the role of gene regulatory evolution in adaptive divergence, here we investigate cis-regulatory changes in gene expression between marine and freshwater ecotypes through allele-specific expression (ASE) in F1 hybrids. Surveying seven ecologically relevant tissues, including three sampled across two developmental stages, we identified cis-regulatory divergence affecting a third of genes, nearly half of which were tissue-specific. Next, we compared allele-specific expression in dental tissues at two timepoints to characterize cis-regulatory changes during development between marine and freshwater fish. Applying a genome-wide test for selection on cis-regulatory changes, we find evidence for lineage-specific selection on several processes between ecotypes, including the Wnt signaling pathway in dental tissues. Finally, we show that genes with ASE, particularly those that are tissue-specific, are strongly enriched in genomic regions of repeated marine-freshwater divergence, supporting an important role for these cis-regulatory differences in parallel adaptive evolution of sticklebacks to freshwater habitats. Altogether, our results provide insight into the cis-regulatory landscape of divergence between stickleback ecotypes across tissues and during development, and support a fundamental role for tissue-specific cis-regulatory changes in rapid adaptation to new environments.
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spelling pubmed-100156192023-03-16 Evolution of Spatial and Temporal cis-Regulatory Divergence in Sticklebacks Mack, Katya L Square, Tyler A Zhao, Bin Miller, Craig T Fraser, Hunter B Mol Biol Evol Discoveries Cis-regulatory changes are thought to play a major role in adaptation. Threespine sticklebacks have repeatedly colonized freshwater habitats in the Northern Hemisphere, where they have evolved a suite of phenotypes that distinguish them from marine populations, including changes in physiology, behavior, and morphology. To understand the role of gene regulatory evolution in adaptive divergence, here we investigate cis-regulatory changes in gene expression between marine and freshwater ecotypes through allele-specific expression (ASE) in F1 hybrids. Surveying seven ecologically relevant tissues, including three sampled across two developmental stages, we identified cis-regulatory divergence affecting a third of genes, nearly half of which were tissue-specific. Next, we compared allele-specific expression in dental tissues at two timepoints to characterize cis-regulatory changes during development between marine and freshwater fish. Applying a genome-wide test for selection on cis-regulatory changes, we find evidence for lineage-specific selection on several processes between ecotypes, including the Wnt signaling pathway in dental tissues. Finally, we show that genes with ASE, particularly those that are tissue-specific, are strongly enriched in genomic regions of repeated marine-freshwater divergence, supporting an important role for these cis-regulatory differences in parallel adaptive evolution of sticklebacks to freshwater habitats. Altogether, our results provide insight into the cis-regulatory landscape of divergence between stickleback ecotypes across tissues and during development, and support a fundamental role for tissue-specific cis-regulatory changes in rapid adaptation to new environments. Oxford University Press 2023-02-20 /pmc/articles/PMC10015619/ /pubmed/36805962 http://dx.doi.org/10.1093/molbev/msad034 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Discoveries
Mack, Katya L
Square, Tyler A
Zhao, Bin
Miller, Craig T
Fraser, Hunter B
Evolution of Spatial and Temporal cis-Regulatory Divergence in Sticklebacks
title Evolution of Spatial and Temporal cis-Regulatory Divergence in Sticklebacks
title_full Evolution of Spatial and Temporal cis-Regulatory Divergence in Sticklebacks
title_fullStr Evolution of Spatial and Temporal cis-Regulatory Divergence in Sticklebacks
title_full_unstemmed Evolution of Spatial and Temporal cis-Regulatory Divergence in Sticklebacks
title_short Evolution of Spatial and Temporal cis-Regulatory Divergence in Sticklebacks
title_sort evolution of spatial and temporal cis-regulatory divergence in sticklebacks
topic Discoveries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10015619/
https://www.ncbi.nlm.nih.gov/pubmed/36805962
http://dx.doi.org/10.1093/molbev/msad034
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