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Pervasive Correlated Evolution in Gene Expression Shapes Cell and Tissue Type Transcriptomes

The evolution and diversification of cell types is a key means by which animal complexity evolves. Recently, hierarchical clustering and phylogenetic methods have been applied to RNA-seq data to infer cell type evolutionary history and homology. A major challenge for interpreting this data is that c...

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Autores principales: Liang, Cong, Musser, Jacob M, Cloutier, Alison, Prum, Richard O, Wagner, Günter P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5800078/
https://www.ncbi.nlm.nih.gov/pubmed/29373668
http://dx.doi.org/10.1093/gbe/evy016
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author Liang, Cong
Musser, Jacob M
Cloutier, Alison
Prum, Richard O
Wagner, Günter P
author_facet Liang, Cong
Musser, Jacob M
Cloutier, Alison
Prum, Richard O
Wagner, Günter P
author_sort Liang, Cong
collection PubMed
description The evolution and diversification of cell types is a key means by which animal complexity evolves. Recently, hierarchical clustering and phylogenetic methods have been applied to RNA-seq data to infer cell type evolutionary history and homology. A major challenge for interpreting this data is that cell type transcriptomes may not evolve independently due to correlated changes in gene expression. This nonindependence can arise for several reasons, such as common regulatory sequences for genes expressed in multiple tissues, that is, pleiotropic effects of mutations. We develop a model to estimate the level of correlated transcriptome evolution (LCE) and apply it to different data sets. The results reveal pervasive correlated transcriptome evolution among different cell and tissue types. In general, tissues related by morphology or developmental lineage exhibit higher LCE than more distantly related tissues. Analyzing new data collected from bird skin appendages suggests that LCE decreases with the phylogenetic age of tissues compared, with recently evolved tissues exhibiting the highest LCE. Furthermore, we show correlated evolution can alter patterns of hierarchical clustering, causing different tissue types from the same species to cluster together. To identify genes that most strongly contribute to the correlated evolution signal, we performed a gene-wise estimation of LCE on a data set with ten species. Removing genes with high LCE allows for accurate reconstruction of evolutionary relationships among tissue types. Our study provides a statistical method to measure and account for correlated gene expression evolution when interpreting comparative transcriptome data.
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spelling pubmed-58000782018-02-12 Pervasive Correlated Evolution in Gene Expression Shapes Cell and Tissue Type Transcriptomes Liang, Cong Musser, Jacob M Cloutier, Alison Prum, Richard O Wagner, Günter P Genome Biol Evol Research Article The evolution and diversification of cell types is a key means by which animal complexity evolves. Recently, hierarchical clustering and phylogenetic methods have been applied to RNA-seq data to infer cell type evolutionary history and homology. A major challenge for interpreting this data is that cell type transcriptomes may not evolve independently due to correlated changes in gene expression. This nonindependence can arise for several reasons, such as common regulatory sequences for genes expressed in multiple tissues, that is, pleiotropic effects of mutations. We develop a model to estimate the level of correlated transcriptome evolution (LCE) and apply it to different data sets. The results reveal pervasive correlated transcriptome evolution among different cell and tissue types. In general, tissues related by morphology or developmental lineage exhibit higher LCE than more distantly related tissues. Analyzing new data collected from bird skin appendages suggests that LCE decreases with the phylogenetic age of tissues compared, with recently evolved tissues exhibiting the highest LCE. Furthermore, we show correlated evolution can alter patterns of hierarchical clustering, causing different tissue types from the same species to cluster together. To identify genes that most strongly contribute to the correlated evolution signal, we performed a gene-wise estimation of LCE on a data set with ten species. Removing genes with high LCE allows for accurate reconstruction of evolutionary relationships among tissue types. Our study provides a statistical method to measure and account for correlated gene expression evolution when interpreting comparative transcriptome data. Oxford University Press 2018-01-23 /pmc/articles/PMC5800078/ /pubmed/29373668 http://dx.doi.org/10.1093/gbe/evy016 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Liang, Cong
Musser, Jacob M
Cloutier, Alison
Prum, Richard O
Wagner, Günter P
Pervasive Correlated Evolution in Gene Expression Shapes Cell and Tissue Type Transcriptomes
title Pervasive Correlated Evolution in Gene Expression Shapes Cell and Tissue Type Transcriptomes
title_full Pervasive Correlated Evolution in Gene Expression Shapes Cell and Tissue Type Transcriptomes
title_fullStr Pervasive Correlated Evolution in Gene Expression Shapes Cell and Tissue Type Transcriptomes
title_full_unstemmed Pervasive Correlated Evolution in Gene Expression Shapes Cell and Tissue Type Transcriptomes
title_short Pervasive Correlated Evolution in Gene Expression Shapes Cell and Tissue Type Transcriptomes
title_sort pervasive correlated evolution in gene expression shapes cell and tissue type transcriptomes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5800078/
https://www.ncbi.nlm.nih.gov/pubmed/29373668
http://dx.doi.org/10.1093/gbe/evy016
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