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Complementary Activities of TELOMERE REPEAT BINDING Proteins and Polycomb Group Complexes in Transcriptional Regulation of Target Genes

机译:端粒重复结合蛋白和多梳基复合物在靶基因转录调控中的互补活性。

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摘要

In multicellular organisms, Polycomb Repressive Complex 1 (PRC1) and PRC2 repress target genes through histone modification and chromatin compaction. Arabidopsis thaliana mutants strongly compromised in the pathway cannot develop differentiated organs. LIKE HETEROCHROMATIN PROTEIN1 (LHP1) is so far the only known plant PRC1 component that directly binds to H3K27me3, the histone modification set by PRC2, and also associates genome-wide with trimethylation of lysine 27 of histone H3 (H3K27me3). Surprisingly, lhp1 mutants show relatively mild phenotypic alterations. To explain this paradox, we screened for genetic enhancers of lhp1 mutants to identify novel components repressing target genes together with, or in parallel to, LHP1. Two enhancing mutations were mapped to TELOMERE REPEAT BINDING PROTEIN1 (TRB1) and its paralog TRB3. We show that TRB1 binds to thousands of genomic sites containing telobox or related cis-elements with a significant increase of sites and strength of binding in the lhp1 background. Furthermore, in combination with lhp1, but not alone, trb1 mutants show increased transcription of LHP1 targets, such as floral meristem identity genes, which are more likely to be bound by TRB1 in the lhp1 background. By contrast, expression of a subset of LHP1-independent TRB1 target genes, many involved in primary metabolism, is decreased in the absence of TRB1 alone. Thus, TRB1 is a bivalent transcriptional modulator that maintains downregulation of Polycomb Group (PcG) target genes in lhp1 mutants, while it sustains high expression of targets that are regulated independently of PcG.
机译:在多细胞生物中,Polycomb Repressive Complex 1(PRC1)和PRC2通过组蛋白修饰和染色质紧缩来抑制靶基因。在该途径中严重受损的拟南芥突变体不能发育分化器官。到目前为止,类似杂色质蛋白1(LHP1)是唯一已知的植物PRC1成分,它直接结合PRC2设置的组蛋白修饰H3K27me3,并且使全基因组与组蛋白H3(H3K27me3)赖氨酸27的三甲基化相关。令人惊讶的是,lhp1突变体表现出相对温和的表型改变。为了解释这一悖论,我们筛选了lhp1突变体的遗传增强子,以确定与LHP1一起或与LHP1平行的新成分抑制目标基因。两个增强突变被映射到端粒重复结合蛋白1(TRB1)及其旁系同源蛋白TRB3。我们显示TRB1结合成千上万个含有端粒盒或相关顺式元件的基因组位点,并且在lhp1背景中结合位点和结合强度显着增加。此外,与lhp1(但不是单独使用)结合使用时,trb1突变体显示LHP1靶标(例如花分生组织同一性基因)的转录增加,这些靶标更可能在lhp1背景中与TRB1结合。相比之下,在没有单独的TRB1的情况下,许多LHP1依赖性TRB1靶基因的子集的表达减少,许多参与初级代谢。因此,TRB1是一种二价转录调节剂,可在lhp1突变体中维持Polycomb Group(PcG)靶基因的下调,同时维持独立于PcG调控的靶标的高表达。

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