Department of Plant Developmental Biology, Max Planck Institute for Plant Breeding Research, Carl-von-Linne Weg 10, 50829 Köln, Germany.
Department of Plant Developmental Biology, Max Planck Institute for Plant Breeding Research, Carl-von-Linne Weg 10, 50829 Köln, Germany.
Dev Cell. 2016 May 9;37(3):254-66. doi: 10.1016/j.devcel.2016.04.001. Epub 2016 Apr 28.
Flowering is initiated in response to environmental and internal cues that are integrated at the shoot apical meristem (SAM). We show that SPL15 coordinates the basal floral promotion pathways required for flowering of Arabidopsis in non-inductive environments. SPL15 directly activates transcription of the floral regulators FUL and miR172b in the SAM during floral induction, whereas its paralog SPL9 is expressed later on the flanks of the SAM. The capacity of SPL15 to promote flowering is regulated by age through miR156, which targets SPL15 mRNA, and gibberellin (GA), which releases SPL15 from DELLAs. Furthermore, SPL15 and the MADS-box protein SOC1 cooperate to promote transcription of their target genes. SPL15 recruits RNAPII and MED18, a Mediator complex component, in a GA-dependent manner, while SOC1 facilitates active chromatin formation with the histone demethylase REF6. Thus, we present a molecular basis for assimilation of flowering signals and transcriptional control at the SAM during flowering.
开花是对环境和内部信号的响应,这些信号在茎尖分生组织(SAM)中整合。我们表明,SPL15 协调了在非诱导环境中开花所需的基本花促进途径。SPL15 在花诱导过程中直接激活 SAM 中花调节因子 FUL 和 miR172b 的转录,而其同源物 SPL9 在 SAM 的侧翼上表达得更晚。SPL15 通过 miR156 靶向 SPL15 mRNA 以及赤霉素(GA)调节其开花能力,GA 可将 SPL15 从 DELLAs 中释放出来。此外,SPL15 和 MADS 盒蛋白 SOC1 合作促进其靶基因的转录。SPL15 以 GA 依赖的方式招募 RNA 聚合酶 II 和 MED18,一种中介复合物成分,而 SOC1 与组蛋白去甲基酶 REF6 一起促进活性染色质的形成。因此,我们提出了在开花过程中 SAM 中开花信号同化和转录控制的分子基础。