生物
拟南芥
MYB公司
转录因子
基因
融合蛋白
细胞生物学
遗传学
原花青素
基因表达
位置克隆
异位表达
突变体
生物化学
抗氧化剂
重组DNA
多酚
作者
Nathalie Nési,Clarisse Jond,Isabelle Debeaujon,Michel Caboche,Loı̈c Lepiniec
出处
期刊:The Plant Cell
[Oxford University Press]
日期:2001-09-01
卷期号:13 (9): 2099-2114
被引量:757
摘要
In Arabidopsis, proanthocyanidins specifically accumulate in the endothelium during early seed development. At least three TRANSPARENT TESTA (TT) genes, TT2, TT8, and TTG1, are necessary for the normal expression of several flavonoid structural genes in immature seed, such as DIHYDROFLAVONOL-4-REDUCTASE and BANYULS (BAN). TT8 and TTG1 were characterized recently and found to code for a basic helix-loop-helix domain transcription factor and a WD-repeat–containing protein, respectively. Here the molecular cloning of the TT2 gene was achieved by T-DNA tagging. TT2 encoded an R2R3 MYB domain protein with high similarity to the rice OsMYB3 protein and the maize COLORLESS1 factor. A TT2–green fluorescent protein fusion protein was located mostly in the nucleus, in agreement with the regulatory function of the native TT2 protein. TT2 expression was restricted to the seed during early embryogenesis, consistent with BAN expression and the proanthocyanidin deposition profile. Finally, in gain-of-function experiments, TT2 was able to induce ectopic expression of BAN in young seedlings and roots in the presence of a functional TT8 protein. Therefore, our results strongly suggest that stringent spatial and temporal BAN expression, and thus proanthocyanidin accumulation, are determined at least partially by TT2.
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