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MOC1 和 MOC3 分蘖芽形成调节剂通过激活水稻 FON1 表达协同促进分蘖芽生长。

Tiller Bud Formation Regulators MOC1 and MOC3 Cooperatively Promote Tiller Bud Outgrowth by Activating FON1 Expression in Rice.

机构信息

State Key Laboratory of Plant Genomics and National Center for Plant Gene Research (Beijing), Institute of Genetics and Developmental Biology, The Innovative Academy of Seed Design, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China; State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou 310006, China.

State Key Laboratory of Plant Genomics and National Center for Plant Gene Research (Beijing), Institute of Genetics and Developmental Biology, The Innovative Academy of Seed Design, Chinese Academy of Sciences, Beijing 100101, China.

出版信息

Mol Plant. 2019 Aug 5;12(8):1090-1102. doi: 10.1016/j.molp.2019.04.008. Epub 2019 Apr 29.

Abstract

Tillering in rice is one of the most important agronomic traits. Rice tiller development can be divided into two main processes: the formation of the axillary bud and its subsequent outgrowth. Several genes critical for bud formation in rice have been identified by genetic studies; however, their molecular functions and relationships are still largely unknown. Here, we report that MONOCULM 1 (MOC1) and MONOCULM 3/TILLERS ABSENT 1/STERILE AND REDUCED TILLERING 1 (MOC3/TAB1/SRT1), two vital regulators for tiller formation in rice, physically interact to regulate tiller bud outgrowth through upregulating the expression of FLORAL ORGAN NUMBER1 (FON1), the homolog of CLAVATA1 in rice. We found that MOC3 is able to directly bind the promoter of FON1 and subsequently activate FON1 expression. MOC1 functions as a co-activator of MOC3, whereas it could not directly bind the FON1 promoter, and further activated FON1 expression in the presence of MOC3. Accordingly, FON1 is highly expressed at axillary meristems and shows remarkably decreased expression levels in moc1 and moc3 mutants. Loss-of-function mutants of FON1 exhibit normal bud formation but defective bud outgrowth and reduced tiller number. Collectively, these results shed light on a joint transcriptional regulatory mechanim by MOC1 and MOC3, and establish a new framework for the control of tiller bud formation and outgrowth.

摘要

分蘖是水稻最重要的农艺性状之一。水稻分蘖的发育可以分为两个主要过程:腋芽的形成和随后的生长。通过遗传研究已经鉴定出几个对水稻芽形成至关重要的基因;然而,它们的分子功能和关系在很大程度上仍然未知。在这里,我们报告 MONOCULM 1(MOC1)和 MONOCULM 3/TILLERS ABSENT 1/STERILE AND REDUCED TILLERING 1(MOC3/TAB1/SRT1),这两个是水稻分蘖形成的重要调节剂,通过上调同源物 CLAVATA1 的表达 FLORAL ORGAN NUMBER1(FON1),物理相互作用来调节分蘖芽的生长。我们发现 MOC3 能够直接结合 FON1 的启动子,随后激活 FON1 的表达。MOC1 作为 MOC3 的共激活因子,而它不能直接结合 FON1 启动子,并且在存在 MOC3 的情况下进一步激活 FON1 的表达。因此,FON1 在腋芽分生组织中高度表达,并且在 moc1 和 moc3 突变体中表达水平显著降低。FON1 的功能丧失突变体表现出正常的芽形成,但芽生长缺陷和分蘖数减少。总之,这些结果揭示了 MOC1 和 MOC3 的联合转录调控机制,并为分蘖芽形成和生长的控制建立了一个新的框架。

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