| Literature DB >> 32778975 |
Qingnan Hao1,2, Yanyan Yang1,2, Zhihui Shan1,2, Haifeng Chen1,2, Chanjuan Zhang1,2, Limiao Chen1,2, Songli Yuan1,2, Xiaojuan Zhang1,2, Shuilian Chen1,2, Zhonglu Yang1,2, Dezhen Qiu1,2, Xinan Zhou3,4.
Abstract
Cystathionine-β-synthase (CBS) domain-containing proteins (CDCPs) constitute a large family in plants, and members of this family have been implicated in a variety of biological processes. However, the precise functions and the underlying mechanisms of most members of this family in plants remain to be elucidated. CBSDUF proteins belong to the CDCP superfamily, which contains one domain of unknown function (DUF21) and an N terminus that is adjacent to two intracellular CBS domains. In this study, a comprehensive genome database analysis of soybean was performed to investigate the role(s) of these CBSDUFs and to explore their nomenclature, classification, chromosomal distribution, exon-intron organization, protein structure, and phylogenetic relationships; the analysis identified a total of 18 putative CBSDUF genes. Using specific protein domains and phylogenetic analysis, the CBSDUF gene family was subdivided into eight groups. The soybean CBSDUF genes showed an uneven distribution on 12 chromosomes of Glycine max. RNA-seq transcriptome data from different tissues in public databases revealed tissue-specific and differential expression profiles of the GmCBSDUFs, and qPCR analysis revealed that certain groups of soybean CBSDUFs are likely involved in specific stress responses. In addition, GmCBSDUF3 transgenic Arabidopsis was subjected to phenotypic analysis under NaCl, PEG, and ABA stress treatments. The overexpression of GmCBSDUF3 could enhance tolerance to drought and salt stress in Arabidopsis. This study presents a first comprehensive look at soybean CBSDUF proteins and provides valuable resources for functionally elucidating this protein subgroup within the CBS domain-containing protein family.Entities:
Keywords: Abiotic stress; CBS domain; CBSDUF genes; Soybean
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Year: 2020 PMID: 32778975 PMCID: PMC7846513 DOI: 10.1007/s10528-020-09991-w
Source DB: PubMed Journal: Biochem Genet ISSN: 0006-2928 Impact factor: 1.890