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通过抑制开花时间基因来确定拟南芥花分生组织的特性。

Specification of Arabidopsis floral meristem identity by repression of flowering time genes.

作者信息

Liu Chang, Zhou Jing, Bracha-Drori Keren, Yalovsky Shaul, Ito Toshiro, Yu Hao

机构信息

Department of Biological Sciences and Temasek Life Sciences Laboratory, National University of Singapore, Singapore 117543, Singapore.

出版信息

Development. 2007 May;134(10):1901-10. doi: 10.1242/dev.003103. Epub 2007 Apr 11.

DOI:10.1242/dev.003103
PMID:17428825
Abstract

Flowering plants produce floral meristems in response to intrinsic and extrinsic flowering inductive signals. In Arabidopsis, the floral meristem identity genes LEAFY (LFY) and APETALA1 (AP1) are activated to play a pivotal role in specifying floral meristems during floral transition. We show here that the emerging floral meristems require AP1 to partly specify their floral identities by directly repressing a group of flowering time genes, including SHORT VEGETATIVE PHASE (SVP), AGAMOUS-LIKE 24 (AGL24) and SUPPRESSOR OF OVEREXPRESSION OF CO1 (SOC1). In wild-type plants, these flowering time genes are normally downregulated in emerging floral meristems. In the absence of AP1, these genes are ectopically expressed, transforming floral meristems into shoot meristems. By post-translational activation of an AP1-GR fusion protein and chromatin immunoprecipitation assays, we further demonstrate the repression of these flowering time genes by induced AP1 activity and in vivo AP1 binding to the cis-regulatory regions of these genes. These findings indicate that once AP1 is activated during the floral transition, it acts partly as a master repressor in floral meristems by directly suppressing the expression of flowering time genes, thus preventing the continuation of the shoot developmental program.

摘要

开花植物会根据内在和外在的开花诱导信号产生花分生组织。在拟南芥中,花分生组织特性基因LEAFY(LFY)和APETALA1(AP1)被激活,在花期转换过程中确定花分生组织时发挥关键作用。我们在此表明,新出现的花分生组织需要AP1通过直接抑制一组开花时间基因,包括SHORT VEGETATIVE PHASE(SVP)、AGAMOUS-LIKE 24(AGL24)和SUPPRESSOR OF OVEREXPRESSION OF CO1(SOC1),来部分确定其花的特性。在野生型植物中,这些开花时间基因在新出现的花分生组织中通常会下调。在没有AP1的情况下,这些基因会异位表达,将花分生组织转化为茎分生组织。通过对AP1-GR融合蛋白的翻译后激活和染色质免疫沉淀分析,我们进一步证明了诱导的AP1活性以及体内AP1与这些基因的顺式调控区域结合对这些开花时间基因的抑制作用。这些发现表明,一旦在花期转换过程中AP1被激活,它在花分生组织中部分地作为一个主要抑制因子,通过直接抑制开花时间基因的表达,从而阻止茎发育程序的继续。

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