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Independent evolution of transcript abundance and gene regulatory dynamics
Changes in gene expression drive novel phenotypes, raising interest in how gene expression evolves. In contrast to the static genome, cells modulate gene expression in response to changing environments. Previous comparative studies focused on specific conditions, describing interspecies variation in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7397873/ https://www.ncbi.nlm.nih.gov/pubmed/32699020 http://dx.doi.org/10.1101/gr.261537.120 |
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author | Krieger, Gat Lupo, Offir Levy, Avraham A. Barkai, Naama |
author_facet | Krieger, Gat Lupo, Offir Levy, Avraham A. Barkai, Naama |
author_sort | Krieger, Gat |
collection | PubMed |
description | Changes in gene expression drive novel phenotypes, raising interest in how gene expression evolves. In contrast to the static genome, cells modulate gene expression in response to changing environments. Previous comparative studies focused on specific conditions, describing interspecies variation in expression levels, but providing limited information about variation across different conditions. To close this gap, we profiled mRNA levels of two related yeast species in hundreds of conditions and used coexpression analysis to distinguish variation in the dynamic pattern of gene expression from variation in expression levels. The majority of genes whose expression varied between the species maintained a conserved dynamic pattern. Cases of diverged dynamic pattern correspond to genes that were induced under distinct subsets of conditions in the two species. Profiling the interspecific hybrid allowed us to distinguish between genes with predominantly cis- or trans-regulatory variation. We find that trans-varying alleles are dominantly inherited, and that cis-variations are often complemented by variations in trans. Based on these results, we suggest that gene expression diverges primarily through changes in expression levels, but does not alter the pattern by which these levels are dynamically regulated. |
format | Online Article Text |
id | pubmed-7397873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-73978732021-01-01 Independent evolution of transcript abundance and gene regulatory dynamics Krieger, Gat Lupo, Offir Levy, Avraham A. Barkai, Naama Genome Res Research Changes in gene expression drive novel phenotypes, raising interest in how gene expression evolves. In contrast to the static genome, cells modulate gene expression in response to changing environments. Previous comparative studies focused on specific conditions, describing interspecies variation in expression levels, but providing limited information about variation across different conditions. To close this gap, we profiled mRNA levels of two related yeast species in hundreds of conditions and used coexpression analysis to distinguish variation in the dynamic pattern of gene expression from variation in expression levels. The majority of genes whose expression varied between the species maintained a conserved dynamic pattern. Cases of diverged dynamic pattern correspond to genes that were induced under distinct subsets of conditions in the two species. Profiling the interspecific hybrid allowed us to distinguish between genes with predominantly cis- or trans-regulatory variation. We find that trans-varying alleles are dominantly inherited, and that cis-variations are often complemented by variations in trans. Based on these results, we suggest that gene expression diverges primarily through changes in expression levels, but does not alter the pattern by which these levels are dynamically regulated. Cold Spring Harbor Laboratory Press 2020-07 /pmc/articles/PMC7397873/ /pubmed/32699020 http://dx.doi.org/10.1101/gr.261537.120 Text en © 2020 Krieger et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Research Krieger, Gat Lupo, Offir Levy, Avraham A. Barkai, Naama Independent evolution of transcript abundance and gene regulatory dynamics |
title | Independent evolution of transcript abundance and gene regulatory dynamics |
title_full | Independent evolution of transcript abundance and gene regulatory dynamics |
title_fullStr | Independent evolution of transcript abundance and gene regulatory dynamics |
title_full_unstemmed | Independent evolution of transcript abundance and gene regulatory dynamics |
title_short | Independent evolution of transcript abundance and gene regulatory dynamics |
title_sort | independent evolution of transcript abundance and gene regulatory dynamics |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7397873/ https://www.ncbi.nlm.nih.gov/pubmed/32699020 http://dx.doi.org/10.1101/gr.261537.120 |
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