Soybean CCA1-like MYB transcription factor GmMYB133 modulates isoflavonoid biosynthesis

被引:39
作者
Bian, Shaomin [1 ]
Li, Ruihua [1 ]
Xia, Siqi [1 ]
Liu, Yajing [1 ]
Jin, Donghao [1 ]
Xie, Xin [1 ]
Dhaubhadel, Sangeeta [2 ,3 ]
Zhai, Lulu [1 ]
Wang, Jingying [1 ]
Li, Xuyan [1 ]
机构
[1] Jilin Univ, Coll Plant Sci, Changchun 130062, Jilin, Peoples R China
[2] Agr & Agri Food Canada, London Res & Dev Ctr, London, ON N5V 4T3, Canada
[3] Western Univ, Dept Biol, London, ON N6A 3K7, Canada
基金
中国国家自然科学基金;
关键词
CCA1-like protein; GmMYB133; lsoflavonoids; Soybean; INTRACELLULAR-LOCALIZATION; CIRCADIAN CLOCK; EXPRESSION; PROTEINS; ACCUMULATION; EVOLUTIONARY;
D O I
10.1016/j.bbrc.2018.11.033
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MYB transcription factors play important roles in the regulation of phenylpropanoid biosynthesis. However, the knowledge regarding the roles of CCA1-like MYBs in phenylpropanoid pathway is limited in plants. Previously, we identified 54 CCA1-like proteins in soybean. In the study, a CCA1-like MYB (GmMYB133) was functionally characterized as a positive regulator in isoflavonoid synthesis. GmMYB133 encodes a 330 aa protein featured with one CCA1 conserved motif. Further analysis indicated that the expression pattern of GmMYB133 was near-perfectly correlated with isoflavonoid accumulation as soybean embryos develop. GmMYB133 over-expression promoted the expression of two key isoflavonoid biosynthetic genes (GmCHS8 and GmlFS2) and increased total isoflavonoid content in hairy roots. Protein-protein interaction assays indicated that GmMYB133 might form hetero- and homodimers with an isoflavonoid regulator GmMYB176 and itself, respectively, while the subcellular localization of GmMYB133 can be altered by its interaction with 14-3-3 protein. These findings provided new insights into the functional roles of CCA1-like MYB proteins in the regulation of phenylpropanoid pathway, and will contribute to the future genetic engineering in the improvement of soybean seed quality. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:324 / 329
页数:6
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