Systematic analysis of the R2R3-MYB transcription factor gene family in Stevia rebaudiana

被引:2
|
作者
Xu, Xiaoyang [1 ,2 ]
Yang, Yongheng [1 ,2 ]
Zhang, Ting [1 ,2 ]
Zhang, Yongxia [1 ,3 ]
Tong, Haiying [1 ,3 ]
Yuan, Haiyan [1 ,2 ]
机构
[1] Jiangsu Prov & Chinese Acad Sci, Inst Bot, Nanjing 210014, Jiangsu, Peoples R China
[2] Jiangsu Key Lab Res & Utilizat Plant Resources, Nanjing 210014, Jiangsu, Peoples R China
[3] Nanjing Bot Garden Mem Sun Yat Sen, Nanjing 210014, Peoples R China
基金
中国国家自然科学基金;
关键词
Expression profiles; Phylogenetic analysis; Stevia; Synteny investigation; ARABIDOPSIS; MYB; BIOSYNTHESIS; EXPRESSION; EVOLUTION; METABOLISM; PATHWAY; DIVERSIFICATION; OVEREXPRESSION; TANSHINONE;
D O I
10.1016/j.indcrop.2024.118123
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
MYB transcription factor (TF) genes are crucial for modulating secondary metabolite biosynthesis in plants. Stevia is a valuable economic crop, and the steviol glycosides produced in its leaves are the most prevalent natural sweeteners. The present research offers a thorough genomic examination of Stevia's MYB TF gene superfamily. We identified 310 genes as putative MYB genes, out of which 176 R2R3-MYB genes were chosen for subsequent analysis. A comparative phylogenetic analysis classified these Stevia R2R3-MYB genes into nine subfamilies, with exon-intron structures and motif compositions strongly supporting this classification. Furthermore, due to its significant expansion, subfamily VIII was divided into 17 clades, and clade VIII -E was unique to Stevia. Synteny analysis revealed that the expansion of members in each subfamily, or each clade within subfamily VIII, was mainly facilitated by whole-genome duplication (WGD) as well as dispersed duplication events. Promoter detection identified multiple classes of cis-regulatory elements that are associated with responses to light, phytohormones, and environmental stressors. Expression analysis revealed that different subfamilies or clades of R2R3-MYB genes exhibited diverse expression profiles across multiple tissue types and at various phases of leaf growth. Meanwhile, SrMYB32, 15, 114/168, 163, 125/126, 33, 153/154 showed significant expression differences in two Stevia varieties with different steviol glycosides content. The present research lays a firm basis for future functional analysis of R2R3-MYBs that play important roles in the biosynthesis of steviol glycosides.
引用
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页数:13
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