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Histone modification pattern evolution after yeast gene duplication

BACKGROUND: Gene duplication and subsequent functional divergence especially expression divergence have been widely considered as main sources for evolutionary innovations. Many studies evidenced that genetic regulatory network evolved rapidly shortly after gene duplication, thus leading to accelera...

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Autores principales: Zou, Yangyun, Su, Zhixi, Huang, Wei, Gu, Xun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3495647/
https://www.ncbi.nlm.nih.gov/pubmed/22776110
http://dx.doi.org/10.1186/1471-2148-12-111
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author Zou, Yangyun
Su, Zhixi
Huang, Wei
Gu, Xun
author_facet Zou, Yangyun
Su, Zhixi
Huang, Wei
Gu, Xun
author_sort Zou, Yangyun
collection PubMed
description BACKGROUND: Gene duplication and subsequent functional divergence especially expression divergence have been widely considered as main sources for evolutionary innovations. Many studies evidenced that genetic regulatory network evolved rapidly shortly after gene duplication, thus leading to accelerated expression divergence and diversification. However, little is known whether epigenetic factors have mediated the evolution of expression regulation since gene duplication. In this study, we conducted detailed analyses on yeast histone modification (HM), the major epigenetics type in this organism, as well as other available functional genomics data to address this issue. RESULTS: Duplicate genes, on average, share more common HM-code patterns than random singleton pairs in their promoters and open reading frames (ORF). Though HM-code divergence between duplicates in both promoter and ORF regions increase with their sequence divergence, the HM-code in ORF region evolves slower than that in promoter region, probably owing to the functional constraints imposed on protein sequences. After excluding the confounding effect of sequence divergence (or evolutionary time), we found the evidence supporting the notion that in yeast, the HM-code may co-evolve with cis- and trans-regulatory factors. Moreover, we observed that deletion of some yeast HM-related enzymes increases the expression divergence between duplicate genes, yet the effect is lower than the case of transcription factor (TF) deletion or environmental stresses. CONCLUSIONS: Our analyses demonstrate that after gene duplication, yeast histone modification profile between duplicates diverged with evolutionary time, similar to genetic regulatory elements. Moreover, we found the evidence of the co-evolution between genetic and epigenetic elements since gene duplication, together contributing to the expression divergence between duplicate genes.
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spelling pubmed-34956472012-11-19 Histone modification pattern evolution after yeast gene duplication Zou, Yangyun Su, Zhixi Huang, Wei Gu, Xun BMC Evol Biol Research Article BACKGROUND: Gene duplication and subsequent functional divergence especially expression divergence have been widely considered as main sources for evolutionary innovations. Many studies evidenced that genetic regulatory network evolved rapidly shortly after gene duplication, thus leading to accelerated expression divergence and diversification. However, little is known whether epigenetic factors have mediated the evolution of expression regulation since gene duplication. In this study, we conducted detailed analyses on yeast histone modification (HM), the major epigenetics type in this organism, as well as other available functional genomics data to address this issue. RESULTS: Duplicate genes, on average, share more common HM-code patterns than random singleton pairs in their promoters and open reading frames (ORF). Though HM-code divergence between duplicates in both promoter and ORF regions increase with their sequence divergence, the HM-code in ORF region evolves slower than that in promoter region, probably owing to the functional constraints imposed on protein sequences. After excluding the confounding effect of sequence divergence (or evolutionary time), we found the evidence supporting the notion that in yeast, the HM-code may co-evolve with cis- and trans-regulatory factors. Moreover, we observed that deletion of some yeast HM-related enzymes increases the expression divergence between duplicate genes, yet the effect is lower than the case of transcription factor (TF) deletion or environmental stresses. CONCLUSIONS: Our analyses demonstrate that after gene duplication, yeast histone modification profile between duplicates diverged with evolutionary time, similar to genetic regulatory elements. Moreover, we found the evidence of the co-evolution between genetic and epigenetic elements since gene duplication, together contributing to the expression divergence between duplicate genes. BioMed Central 2012-07-09 /pmc/articles/PMC3495647/ /pubmed/22776110 http://dx.doi.org/10.1186/1471-2148-12-111 Text en Copyright ©2012 2012 Zou et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zou, Yangyun
Su, Zhixi
Huang, Wei
Gu, Xun
Histone modification pattern evolution after yeast gene duplication
title Histone modification pattern evolution after yeast gene duplication
title_full Histone modification pattern evolution after yeast gene duplication
title_fullStr Histone modification pattern evolution after yeast gene duplication
title_full_unstemmed Histone modification pattern evolution after yeast gene duplication
title_short Histone modification pattern evolution after yeast gene duplication
title_sort histone modification pattern evolution after yeast gene duplication
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3495647/
https://www.ncbi.nlm.nih.gov/pubmed/22776110
http://dx.doi.org/10.1186/1471-2148-12-111
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