Literature DB >> 33552724

Genome-wide identification, evolution, expression, and alternative splicing profiles of peroxiredoxin genes in cotton.

Yulong Feng1, Renhui Wei2, Aiying Liu2, Senmiao Fan2, JinCan Che1, Zhen Zhang2, Baoming Tian1, Youlu Yuan2, Gongyao Shi1, Haihong Shang1,2.   

Abstract

Peroxiredoxin (PRX) is a ubiquitous thioredoxin-dependent peroxidase that can eliminate excessive free radicals produced by stress and protect cells from oxidative damage. PRXs are also involved in reactive oxygen species (ROS)- and redox-dependent signaling by performing redox interactions with other proteins and modify their redox status. At present, PRX family identification, evolution and regulation research has been conducted in some plants; however, systematic research about this family is lacking in cotton. In this study, a total of 44 PRXs were identified in the cotton genome. Phylogenetic and conserved active site analyses showed that the PRXs were divided into six subfamilies according to the conserved site (PxxxTxxC…S…W/F) and conserved cysteinyl residues positions. Segmental duplication and polyploid events were the main methods for PRX family expansion, and the PRXs of diploid G. arboreum were the donors of PRXs in the D subgenomes of allotetraploid G. hirsutum and G. barbadense during the evolution of the PRX family. qRT-PCR analysis confirmed that cis-acting elements play important roles in regulating the expression of PRXs. Alternative splicing events occurred in GhPRX14-D that can increased the complexity of transcripts in G. hirsutum. Subcellular localization showed that most PRX members were located in chloroplasts, the cytoplasmic membrane and the nucleus. Our results provide systematic support for a better understanding of PRXs in cotton and a starting point for further studies of the specific functions of PRXs in cotton. ©2021 Feng et al.

Entities:  

Keywords:  Alternative; Evolution; Expression; Localization; Peroxiredoxin

Year:  2021        PMID: 33552724      PMCID: PMC7819121          DOI: 10.7717/peerj.10685

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


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