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A Feed-Forward Repression Mechanism Anchors the Sin3/Histone Deacetylase and N-CoR/SMRT Corepressors on Chromatin

机译:前馈抑制机制将染色质上的Sin3 /组蛋白脱乙酰基酶和N-CoR / SMRT共抑制因子锚定

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摘要

Transcription in eukaryotes is governed in part by histone acetyltransferase (HAT)- and histone deacetylase (HDAC)-containing complexes that are recruited via activators and repressors, respectively. Here, we show that the Sin3/HDAC and N-CoR/SMRT corepressor complexes repress transcription from histone H3- and/or H4-acetylated nucleosomal templates in vitro. Repression of histone H3-acetylated templates was completely dependent on the histone deacetylase activity of the corepressor complexes, whereas this activity was not required to repress H4-acetylated templates. Following deacetylation, both complexes become stably anchored in a repressor-independent manner to nucleosomal templates containing hypoacetylated histone H3, but not H4, resulting in dominance of repression over activation. The observed stable anchoring of corepressor complexes casts doubt on the view of a dynamic balance between readily exchangeable HAT and HDAC activities regulating transcription and implies that pathways need to be in place to actively remove HDAC complexes from hypoacetylated promoters to switch on silent genes.
机译:真核生物中的转录部分受含组蛋白乙酰转移酶(HAT)和含组蛋白脱乙酰基酶(HDAC)的复合物支配,这些复合物分别通过激活剂和阻遏剂募集。在这里,我们显示Sin3 / HDAC和N-CoR / SMRT核心复合物在体外抑制组蛋白H3和/或H4乙酰化的核小体模板的转录。组蛋白H3乙酰化模板的抑制完全依赖于共加压复合物的组蛋白脱乙酰基酶活性,而抑制H4乙酰化模板不需要此活性。脱乙酰基作用后,两种复合物都以阻遏物独立的方式稳定地锚定在含有低乙酰化组蛋白H3而不是H4的核小体模板上,从而导致抑制作用高于激活作用。观察到的稳定的心脏加压因子复合物锚定,使人们对容易交换的HAT和调节转录的HDAC活性之间的动态平衡观点持怀疑态度,并暗示需要建立通路以从低乙酰化启动子中主动除去HDAC复合物以开启沉默基因。

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