Literature DB >> 33505781

In situ dissecting the evolution of gene duplication with different histone modification patterns based on high-throughput data analysis in Arabidopsis thaliana.

Jingjing Wang1,2,3,4, Yuriy L Orlov5,6,7, Xue Li3,8, Yincong Zhou2,3, Yongjing Liu2,3, Chunhui Yuan4,9, Ming Chen1,2,3.   

Abstract

BACKGROUND: Genetic regulation is known to contribute to the divergent expression of duplicate genes; however, little is known about how epigenetic modifications regulate the expression of duplicate genes in plants.
METHODS: The histone modification (HM) profile patterns of different modes of gene duplication, including the whole genome duplication, proximal duplication, tandem duplication and transposed duplication were characterized based on ChIP-chip or ChIP-seq datasets. In this study, 10 distinct HM marks including H2Bub, H3K4me1, H3K4me2, H3K4me3, H3K9ac, H3K9me2, H3K27me1, H3K27me3, H3K36me3 and H3K14ac were analyzed. Moreover, the features of gene duplication with different HM patterns were characterized based on 88 RNA-seq datasets of Arabidopsis thaliana.
RESULTS: This study showed that duplicate genes in Arabidopsis have a more similar HM pattern than single-copy genes in both their promoters and protein-coding regions. The evolution of HM marks is found to be coupled with coding sequence divergence and expression divergence after gene duplication. We found that functionally selective constraints may impose on epigenetic evolution after gene duplication. Furthermore, duplicate genes with distinct functions have more divergence in histone modification compared with the ones with the same function, while higher expression divergence is found with mutations of chromatin modifiers. This study shows the role of epigenetic marks in regulating gene expression and functional divergence after gene duplication in plants based on sequencing data.
© 2021 Wang et al.

Entities:  

Keywords:  A. thaliana; Bioinformatics; ChIP-chip; Epigenetic pattern evolution; Gene duplication; Histone modifications; Plant genome; RNA-seq

Year:  2021        PMID: 33505781      PMCID: PMC7792519          DOI: 10.7717/peerj.10426

Source DB:  PubMed          Journal:  PeerJ        ISSN: 2167-8359            Impact factor:   2.984


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