Genome-wide identification and characterization of R2R3MYB family in Cucumis sativus.

<h4>Background</h4>The R2R3MYB proteins comprise one of the largest families of transcription factors in plants. Although genome-wide analysis of this family has been carried out in some species, little is known about R2R3MYB genes in cucumber (Cucumis sativus L.).<h4>Principal fin...

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Main Authors: Qiang Li, Cunjia Zhang, Jing Li, Lina Wang, Zhonghai Ren
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23110079/pdf/?tool=EBI
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spelling doaj-53748af72c8141b9b283088856ed0bf02021-03-04T00:09:33ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01710e4757610.1371/journal.pone.0047576Genome-wide identification and characterization of R2R3MYB family in Cucumis sativus.Qiang LiCunjia ZhangJing LiLina WangZhonghai Ren<h4>Background</h4>The R2R3MYB proteins comprise one of the largest families of transcription factors in plants. Although genome-wide analysis of this family has been carried out in some species, little is known about R2R3MYB genes in cucumber (Cucumis sativus L.).<h4>Principal findings</h4>This study has identified 55 R2R3MYB genes in the latest cucumber genome and the CsR2R3MYB family contained the smallest number of identified genes compared to other species that have been studied due to the absence of recent gene duplication events. These results were also supported by genome distribution and gene duplication analysis. Phylogenetic analysis showed that they could be classified into 11 subgroups. The evolutionary relationships and the intron-exon organizations that showed similarities with Arabidopsis, Vitis and Glycine R2R3MYB proteins were also analyzed and suggested strong gene conservation but also the expansions of particular functional genes during the evolution of the plant species. In addition, we found that 8 out of 55 (∼14.54%) cucumber R2R3MYB genes underwent alternative splicing events, producing a variety of transcripts from a single gene, which illustrated the extremely high complexity of transcriptome regulation. Tissue-specific expression profiles showed that 50 cucumber R2R3MYB genes were expressed in at least one of the tissues and the other 5 genes showed very low expression in all tissues tested, which suggested that cucumber R2R3MYB genes took part in many cellular processes. The transcript abundance level analysis during abiotic conditions (NaCl, ABA and low temperature treatments) identified a group of R2R3MYB genes that responded to one or more treatments.<h4>Conclusions</h4>This study has produced a comparative genomics analysis of the cucumber R2R3MYB gene family and has provided the first steps towards the selection of CsR2R3MYB genes for cloning and functional dissection that can be used in further studies to uncover their roles in cucumber growth and development.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23110079/pdf/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Qiang Li
Cunjia Zhang
Jing Li
Lina Wang
Zhonghai Ren
spellingShingle Qiang Li
Cunjia Zhang
Jing Li
Lina Wang
Zhonghai Ren
Genome-wide identification and characterization of R2R3MYB family in Cucumis sativus.
PLoS ONE
author_facet Qiang Li
Cunjia Zhang
Jing Li
Lina Wang
Zhonghai Ren
author_sort Qiang Li
title Genome-wide identification and characterization of R2R3MYB family in Cucumis sativus.
title_short Genome-wide identification and characterization of R2R3MYB family in Cucumis sativus.
title_full Genome-wide identification and characterization of R2R3MYB family in Cucumis sativus.
title_fullStr Genome-wide identification and characterization of R2R3MYB family in Cucumis sativus.
title_full_unstemmed Genome-wide identification and characterization of R2R3MYB family in Cucumis sativus.
title_sort genome-wide identification and characterization of r2r3myb family in cucumis sativus.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description <h4>Background</h4>The R2R3MYB proteins comprise one of the largest families of transcription factors in plants. Although genome-wide analysis of this family has been carried out in some species, little is known about R2R3MYB genes in cucumber (Cucumis sativus L.).<h4>Principal findings</h4>This study has identified 55 R2R3MYB genes in the latest cucumber genome and the CsR2R3MYB family contained the smallest number of identified genes compared to other species that have been studied due to the absence of recent gene duplication events. These results were also supported by genome distribution and gene duplication analysis. Phylogenetic analysis showed that they could be classified into 11 subgroups. The evolutionary relationships and the intron-exon organizations that showed similarities with Arabidopsis, Vitis and Glycine R2R3MYB proteins were also analyzed and suggested strong gene conservation but also the expansions of particular functional genes during the evolution of the plant species. In addition, we found that 8 out of 55 (∼14.54%) cucumber R2R3MYB genes underwent alternative splicing events, producing a variety of transcripts from a single gene, which illustrated the extremely high complexity of transcriptome regulation. Tissue-specific expression profiles showed that 50 cucumber R2R3MYB genes were expressed in at least one of the tissues and the other 5 genes showed very low expression in all tissues tested, which suggested that cucumber R2R3MYB genes took part in many cellular processes. The transcript abundance level analysis during abiotic conditions (NaCl, ABA and low temperature treatments) identified a group of R2R3MYB genes that responded to one or more treatments.<h4>Conclusions</h4>This study has produced a comparative genomics analysis of the cucumber R2R3MYB gene family and has provided the first steps towards the selection of CsR2R3MYB genes for cloning and functional dissection that can be used in further studies to uncover their roles in cucumber growth and development.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23110079/pdf/?tool=EBI
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