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首页> 外文期刊>PLoS Genetics >Arabidopsis TFL2/LHP1 Specifically Associates with Genes Marked by Trimethylation of Histone H3 Lysine 27
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Arabidopsis TFL2/LHP1 Specifically Associates with Genes Marked by Trimethylation of Histone H3 Lysine 27

机译:拟南芥TFL2 / LHP1与组蛋白H3赖氨酸三甲基化标记的基因特别相关27

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TERMINAL FLOWER 2/LIKE HETEROCHROMATIN PROTEIN 1 (TFL2/LHP1) is the only Arabidopsis protein with overall sequence similarity to the HETEROCHROMATIN PROTEIN 1 (HP1) family of metazoans and S. pombe. TFL2/LHP1 represses transcription of numerous genes, including the flowering-time genes FLOWERING LOCUS T (FT) and FLOWERING LOCUS C (FLC), as well as the floral organ identity genes AGAMOUS (AG) and APETALA 3 (AP3). These genes are also regulated by proteins of the Polycomb repressive complex 2 (PRC2), and it has been proposed that TFL2/LHP1 represents a potential stabilizing factor of PRC2 activity. Here we show by chromatin immunoprecipitation and hybridization to an Arabidopsis Chromosome 4 tiling array (ChIP-chip) that TFL2/LHP1 associates with hundreds of small domains, almost all of which correspond to genes located within euchromatin. We investigated the chromatin marks to which TFL2/LHP1 binds and show that, in vitro, TFL2/LHP1 binds to histone H3 di- or tri-methylated at lysine 9 (H3K9me2 or H3K9me3), the marks recognized by HP1, and to histone H3 trimethylated at lysine 27 (H3K27me3), the mark deposited by PRC2. However, in vivo TFL2/LHP1 association with chromatin occurs almost exclusively and co-extensively with domains marked by H3K27me3, but not H3K9me2 or -3. Moreover, the distribution of H3K27me3 is unaffected in lhp1 mutant plants, indicating that unlike PRC2 components, TFL2/LHP1 is not involved in the deposition of this mark. Rather, our data suggest that TFL2/LHP1 recognizes specifically H3K27me3 in vivo as part of a mechanism that represses the expression of many genes targeted by PRC2.
机译:TERMINAL FLOWER 2 / LIKE CHROMOCROMATIN PROTININ 1(TFL2 / LHP1)是唯一具有与后生动物和粟酒裂殖酵母HETEROCHROMATIN蛋白1(HP1)家族总体序列相似的拟南芥蛋白。 TFL2 / LHP1抑制许多基因的转录,包括开花期基因FLOWERING LOCUS T(FT)和FLOWERING LOCUS C(FLC),以及花器官同一性基因AGAMOUS(AG)和APETALA 3(AP3)。这些基因也受Polycomb抑制复合物2(PRC2)的蛋白质调控,并且有人提出TFL2 / LHP1代表PRC2活性的潜在稳定因子。在这里,我们通过染色质免疫沉淀和与拟南芥染色体4切片阵列(ChIP-chip)的杂交显示,TFL2 / LHP1与数百个小域相关,几乎所有小域都对应于常染色质中的基因。我们研究了TFL2 / LHP1结合的染色质标记,并显示了TFL2 / LHP1在体外与赖氨酸9(H3K9me2或H3K9me3)的二甲基或三甲基化的组蛋白H3结合,HP1识别的标记以及与组蛋白H3的结合在赖氨酸27(H3K27me3)处三甲基化,该标记由PRC2保藏。但是,体内TFL2 / LHP1与染色质的缔合几乎仅与H3K27me3标记的结构域共同发生,而与H3K9me2或-3无关。此外,H3K27me3的分布在lhp1突变植物中不受影响,表明与PRC2组件不同,TFL2 / LHP1不参与该标记的沉积。而是,我们的数据表明,TFL2 / LHP1在体内特异性识别H3K27me3,这是抑制PRC2靶向的许多基因表达的机制的一部分。

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