| Literature DB >> 33854830 |
Mengyao Li1, Qi He1, Ying Huang2, Ya Luo1, Yong Zhang1, Qing Chen1, Yan Wang1,3, Yuanxiu Lin1,3, Yunting Zhang1,3, Zejing Liu1, Xiao-Rong Wang1,3, Haoru Tang1,3.
Abstract
Sucrose synthase (SUS) plays an important role in sucrose metabolism and plant development. The SUS gene family has been identified in many plants, however, there is no definitive study of SUS gene in Brassica juncea. In this study, 14 SUS family genes were identified and comprehensively analyzed using bioinformatics tools. The analyzed parameters included their family member characteristics, chromosomal locations, gene structures and phylogenetic as well as transcript expression profiles. Phylogenetic analysis revealed that the 14 members could be allocated into three groups: SUS I, SUS II and SUS III. Comparisons of the exon/intron structure of the mustard SUS gene indicated that its structure is highly conserved. The conserved structure is attributed to purification selection during evolution. Expansion of the SUS gene family is associated with fragment and tandem duplications of the mustard SUS gene family. Collinearity analysis among species revealed that the SUS gene family could be lost or mutated to varying degrees after the genome was doubled, or when Brassica rapa and Brassica nigra hybridized to form Brassica juncea. The expression patterns of BjuSUSs vary among different stages of mustard stem swelling. Transcriptomics revealed that the BjuSUS01-04 expression levels were the most elevated. It has been hypothesized that they play an important role in sucrose metabolism during stem development. The expression levels of some BjuSUSs were significantly up-regulated when they were treated with plant hormones. However, when subjected to abiotic stress factors, their expression levels were suppressed. This study establishes SUS gene functions during mustard stem development and stress.Entities:
Keywords: Brassica juncea; Gene expression; Phylogenetic analysis; Sucrose synthase; Syntenic analysis
Year: 2021 PMID: 33854830 PMCID: PMC7953879 DOI: 10.7717/peerj.10878
Source DB: PubMed Journal: PeerJ ISSN: 2167-8359 Impact factor: 2.984