期刊
PLANT MOLECULAR BIOLOGY
卷 98, 期 1-2, 页码 169-183出版社
SPRINGER
DOI: 10.1007/s11103-018-0773-2
关键词
Prunus; Anthocyanin coloration; R2R3-MYB TF; bHLH gene; DNA-binding affinity; Site-directed mutation
资金
- National Natural Science Foundation of China [31672134]
- China Agriculture Research System [CARS-30]
- Overseas Construction Plan for Science and Education Base, China-Africa Center for Research and Education, Chinese Academy of Sciences [SAJC201327]
R2R3-MYB genes play a pivotal role in regulating anthocyanin accumulation. Here, we report two tandemly duplicated R2R3-MYB genes in peach, PpMYB10.1 and PpMYB10.2, with the latter showing lower ability to induce anthocyanin accumulation than the former. Site-directed mutation assay revealed two amino acid changes in the R3 repeat, Arg/Lys(66) and Gly/Arg(93), responsible for functional divergence between these two PpMYB10 genes. Anthocyanin-promoting activity of PpMYB10.2 was significantly increased by a single amino acid replacement of Arg(93) with Gly(93). However, either the Gly(93) Arg(93) or Arg(66) Lys(66) substitutions alone showed little impact on anthocyanin-promoting activity of PpMYB10.1, but simultaneous substitutions caused a significant decrease. Reciprocal substitution of Arg/Gly(93) could significantly alter binding affinity to PpbHLH3, while the Arg(66) Lys(66) substitution is predicted to affect the folding of the MYB DNA-binding domain, instead of PpbHLH3-binding affinity. Overall, the change of anthocyanin-promoting activity was accompanied with that of bHLH-binding affinity, suggesting that DNA-binding affinity of R2R3-MYBs depends on their bHLH partners. Our study is helpful for understanding of functional evolution of R2R3-MYBs and their interaction with DNA targets.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据