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拟南芥开花时间调控中多种组蛋白甲基化的组合功能。

Combinatorial functions of diverse histone methylations in Arabidopsis thaliana flowering time regulation.

机构信息

Institut de Biologie Moléculaire des Plantes du CNRS, Université de Strasbourg, 12 rue du Général Zimmer, Strasbourg, 67084, France.

出版信息

New Phytol. 2014 Jan;201(1):312-322. doi: 10.1111/nph.12493. Epub 2013 Sep 18.

DOI:10.1111/nph.12493
PMID:24102415
Abstract

Previous studies in Arabidopsis thaliana have identified several histone methylation enzymes, including Arabidopsis trithorax1 (ATX1)/set domain group 27 (SDG27), ATX2/SDG30, LSD1-LIKE1 (LDL1), LDL2, SDG8, SDG25, and curly leaf (CLF)/SDG1, as regulators of the key flowering repressor flowering locus C (FLC) and the florigen flowering locus T (FT). However, the combinatorial functions of these enzymes remain largely uninvestigated. Here, we investigated functional interplays of different histone methylation enzymes by studying higher order combinations of their corresponding gene mutants. We showed that H3K4me2/me3 and H3K36me3 depositions occur largely independently and that SDG8-mediated H3K36me3 overrides ATX1/ATX2-mediated H3K4me2/me3 or LDL1/LDL2-mediated H3K4 demethylation in regulating FLC expression and flowering time. By contrast, a reciprocal inhibition was observed between deposition of the active mark H3K4me2/me3 and/or H3K36me3 and deposition of the repressive mark H3K27me3 at both FLC and FT chromatin; and the double mutants sdg8 clf and sdg25 clf displayed enhanced early-flowering phenotypes of the respective single mutants. Collectively, our results provide important insights into the interactions of different types of histone methylation and enzymes in the regulation of FLC and FT expression in flowering time control.

摘要

先前在拟南芥中的研究已经鉴定出几种组蛋白甲基化酶,包括拟南芥 trithorax1(ATX1)/SET 结构域组 27(SDG27)、ATX2/SDG30、LSD1-LIKE1(LDL1)、LDL2、SDG8、SDG25 和卷叶(CLF)/SDG1,它们作为关键开花抑制因子 FLOWERING LOCUS C(FLC)和开花诱导因子 FT 的调节剂。然而,这些酶的组合功能在很大程度上仍未得到研究。在这里,我们通过研究它们相应基因突变体的更高阶组合来研究不同组蛋白甲基化酶的功能相互作用。我们表明 H3K4me2/me3 和 H3K36me3 的沉积在很大程度上是独立发生的,并且 SDG8 介导的 H3K36me3 可以覆盖 ATX1/ATX2 介导的 H3K4me2/me3 或 LDL1/LDL2 介导的 H3K4 去甲基化,从而调节 FLC 的表达和开花时间。相比之下,在 FLC 和 FT 染色质上,活性标记 H3K4me2/me3 和/或 H3K36me3 的沉积和抑制性标记 H3K27me3 的沉积之间观察到相互抑制;并且 sdg8 clf 和 sdg25 clf 的双突变体表现出各自单突变体的早花表型增强。总的来说,我们的研究结果为不同类型的组蛋白甲基化和酶在调节 FLC 和 FT 表达以及开花时间控制中的相互作用提供了重要的见解。

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