Differential control of seed primary dormancy in Arabidopsis ecotypes by the transcription factor SPATULA

脱落酸 休眠 赤霉素 拟南芥 生物 发芽 种子休眠 转录因子 生态型 赤霉素 细胞生物学 植物 遗传学 基因 突变体
作者
Fabián E. Vaistij,Yinbo Gan,Steven Penfield,Alison D. Gilday,Anuja Dave,Zhesi He,Eve‐Marie Josse,Giltsu Choi,Karen Halliday,Ian A. Graham
出处
期刊:Proceedings of the National Academy of Sciences of the United States of America [Proceedings of the National Academy of Sciences]
卷期号:110 (26): 10866-10871 被引量:114
标识
DOI:10.1073/pnas.1301647110
摘要

Freshly matured seeds exhibit primary dormancy, which prevents germination until environmental conditions are favorable. The establishment of dormancy occurs during seed development and involves both genetic and environmental factors that impact on the ratio of two antagonistic phytohormones: abscisic acid (ABA), which promotes dormancy, and gibberellic acid, which promotes germination. Although our understanding of dormancy breakage in mature seeds is well advanced, relatively little is known about the mechanisms involved in establishing dormancy during seed maturation. We previously showed that the SPATULA (SPT) transcription factor plays a key role in regulating seed germination. Here we investigate its role during seed development and find that, surprisingly, it has opposite roles in setting dormancy in Landsberg erecta and Columbia Arabidopsis ecotypes. We also find that SPT regulates expression of five transcription factor encoding genes: ABA-INSENSITIVE4 ( ABI4 ) and ABI5 , which mediate ABA signaling; REPRESSOR-OF-GA ( RGA ) and RGA-LIKE3 involved in gibberellic acid signaling; and MOTHER-OF-FT-AND-TFL1 ( MFT ) that we show here promotes Arabidopsis seed dormancy. Although ABI4 , RGA , and MFT are repressed by SPT, ABI5 and RGL3 are induced. Furthermore, we show that RGA , MFT , and ABI5 are direct targets of SPT in vivo. We present a model in which SPT drives two antagonistic “dormancy-repressing” and “dormancy-promoting” routes that operate simultaneously in freshly matured seeds. Each of these routes has different impacts and this in turn explains the opposite effect of SPT on seed dormancy of the two ecotypes analyzed here.

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