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Regulation of Arabidopsis Flowering by the Histone Mark Readers MRG1/2 via Interaction with CONSTANS to Modulate FT Expression

机译:组蛋白标记阅读器MRG1 / 2通过与CONSTANS相互作用调节FT表达来调节拟南芥开花。

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摘要

Day-length is important for regulating the transition to reproductive development (flowering) in plants. In the model plant Arabidopsis thaliana, the transcription factor CONSTANS (CO) promotes expression of the florigen FLOWERING LOCUS T (FT), constituting a key flowering pathway under long-day photoperiods. Recent studies have revealed that FT expression is regulated by changes of histone modification marks of the FT chromatin, but the epigenetic regulators that directly interact with the CO protein have not been identified. Here, we show that the Arabidopsis Morf Related Gene (MRG) group proteins MRG1 and MRG2 act as H3K4me3/H3K36me3 readers and physically interact with CO to activate FT expression. In vitro binding analyses indicated that the chromodomains of MRG1 and MRG2 preferentially bind H3K4me3/H3K36me3 peptides. The mrg1 mrg2 double mutant exhibits reduced mRNA levels of FT, but not of CO, and shows a late-flowering phenotype under the long-day but not short-day photoperiod growth conditions. MRG2 associates with the chromatin of FT promoter in a way dependent of both CO and H3K4me3/H3K36me3. Vice versa, loss of MRG1 and MRG2 also impairs CO binding at the FT promoter. Crystal structure analyses of MRG2 bound with H3K4me3/H3K36me3 peptides together with mutagenesis analysis in planta further demonstrated that MRG2 function relies on its H3K4me3/H3K36me3-binding activity. Collectively, our results unravel a novel chromatin regulatory mechanism, linking functions of MRG1 and MRG2 proteins, H3K4/H3K36 methylations, and CO in FT activation in the photoperiodic regulation of flowering time in plants.
机译:日长对于调节植物向生殖发育(开花)的过渡很重要。在模型植物拟南芥中,转录因子CONSTANS(CO)促进了荧光素FLOWERING LOCUS T(FT)的表达,构成了长期光周期下的关键开花途径。最近的研究表明,FT表达受FT染色质的组蛋白修饰标记变化的调控,但是尚未发现与CO蛋白直接相互作用的表观遗传调控因子。在这里,我们显示拟南芥Morf相关基因(MRG)组蛋白MRG1和MRG2充当H3K4me3 / H3K36me3读者,并与CO物理相互作用以激活FT表达。体外结合分析表明,MRG1和MRG2的染色体结构域优先结合H3K4me3 / H3K36me3肽。 mrg1 mrg2双重突变体表现出降低的FT mRNA水平,但不降低CO的mRNA水平,并且在长日而不是短日光周期生长条件下显示出迟开花表型。 MRG2以依赖CO和H3K4me3 / H3K36me3的方式与FT启动子的染色质缔合。反之亦然,MRG1和MRG2的丢失也会损害FT启动子上的CO结合。与H3K4me3 / H3K36me3肽结合的MRG2的晶体结构分析以及在植物中的诱变分析 进一步证明MRG2的功能依赖于其H3K4me3 / H3K36me3结合活性。总的来说,我们的结果揭示了一种新颖的染色质调节机制,将MRG1和MRG2蛋白,H3K4 / H3K36甲基化和CO在 FT 激活中的功能联系起来,从而周期性地调节植物的开花时间。

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