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WRKY41通过直接调控ABI3转录水平而非在脱落酸下游来控制拟南芥种子休眠。

WRKY41 controls Arabidopsis seed dormancy via direct regulation of ABI3 transcript levels not downstream of ABA.

作者信息

Ding Zhong Jie, Yan Jing Ying, Li Gui Xin, Wu Zhong Chang, Zhang Shu Qun, Zheng Shao Jian

机构信息

State Key Laboratory of Plant Physiology and Biochemistry, College of Life Sciences, Zhejiang University, Hangzhou, 310058, China.

出版信息

Plant J. 2014 Sep;79(5):810-23. doi: 10.1111/tpj.12597. Epub 2014 Jul 28.

Abstract

Although seed dormancy is an important agronomic trait, its molecular basis is poorly understood. ABSCISIC ACID INSENSITIVE 3 (ABI3) plays an essential role in the establishment of seed dormancy. Here, we show that the lack of a seed-expressed WRKY transcription factor, WRKY41, confers reduced primary seed dormancy and thermoinhibition, phenotypes resembling those for a lack of ABI3. Loss-of-function abi3-17 and wrky41 alleles also both confer reduced sensitivity to ABA during germination and early seedling growth. Absence of WRKY41 decreases ABI3 transcript abundance in maturing and imbibed seeds, whereas transgenically overexpressing WRKY41 increases ABI3 expression. Moreover, transgenic overexpression of ABI3 completely restores seed dormancy phenotypes on wrky41. ChIP-qPCR and EMSA reveal that WRKY41 binds directly to the ABI3 promoter through three adjacent W-boxes, and a transactivation assay indicates that these W-boxes are essential for ABI3 expression. Whilst RT-qPCR analysis shows that the regulation of ABI3 by WRKY41 is not through ABA and other factors known to promote ABI3 transcription during seed maturation and germination, we also show that high concentrations of ABA might promote negative feedback regulation of WRKY41 expression. Finally, analysis of the wrky41 aba2 double mutant confirms that WRKY41 and ABA collaboratively regulate ABI3 expression and seed dormancy. In summary, our results demonstrate that WRKY41 is an important regulator of ABI3 expression, and hence of seed dormancy.

摘要

尽管种子休眠是一个重要的农艺性状,但其分子基础仍知之甚少。脱落酸不敏感3(ABI3)在种子休眠的建立中起关键作用。在此,我们表明,种子中表达的WRKY转录因子WRKY41的缺失导致初级种子休眠和热抑制降低,其表型与缺乏ABI3时相似。功能缺失的abi3-17和wrky41等位基因在种子萌发和幼苗早期生长过程中对脱落酸(ABA)的敏感性也均降低。WRKY41的缺失降低了成熟种子和吸胀种子中ABI3的转录丰度,而转基因过量表达WRKY41则增加了ABI3的表达。此外,ABI3的转基因过量表达完全恢复了wrky41的种子休眠表型。染色质免疫沉淀定量PCR(ChIP-qPCR)和电泳迁移率变动分析(EMSA)表明,WRKY41通过三个相邻的W盒直接结合到ABI3启动子上,并且反式激活分析表明这些W盒对ABI3的表达至关重要。虽然逆转录定量PCR(RT-qPCR)分析表明WRKY41对ABI3的调控不是通过ABA以及其他已知在种子成熟和萌发过程中促进ABI3转录的因子,但我们也表明高浓度的ABA可能促进WRKY41表达的负反馈调节。最后,对wrky41 aba2双突变体的分析证实,WRKY41和ABA协同调节ABI3的表达和种子休眠。总之,我们的结果表明WRKY41是ABI3表达的重要调节因子,因此也是种子休眠的重要调节因子。

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