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TRRAP and GCN5 are used by c-Myc to activate RNA polymerase Ⅲ transcription

机译:c-Myc使用TRRAP和GCN5激活RNA聚合酶Ⅲ转录

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Activation of RNA polymerase (pol) Ⅱ transcription by c-Myc generally involves recruitment of histone acetyltransferases and acet-ylation of histones H3 and H4. Here, we describe the mechanism used by c-Myc to activate pol Ⅲ transcription of tRNA and 5S rRNA genes. Within 2 h of its induction, c-Myc appears at these genes along with the histone acetyltransferase GCN5 and the cofactor TRRAP. At the same time, occupancy of the pol Ⅲ-specific factor TFⅢB increases and histone H3 becomes hyperacetylated, but increased histone H4 acetylation is not detected at these genes. The rapid acetylation of histone H3 and promoter assembly of TFⅢB, c-Myc, GCN5, and TRRAP are followed by recruitment of pol Ⅲ and transcriptional induction. The selective acetylation of histone H3 distinguishes pol Ⅲ activation by c-Myc from mechanisms observed in other systems.
机译:c-Myc激活RNA聚合酶(pol)Ⅱ转录通常涉及组蛋白乙酰转移酶的募集和组蛋白H3和H4的乙酰化。在这里,我们描述了c-Myc激活tRNA和5S rRNA基因的polⅢ转录的机制。在诱导的2小时内,c-Myc与组蛋白乙酰转移酶GCN5和辅因子TRRAP一起出现在这些基因上。同时,polⅢ特异性因子TFⅢB的占有率增加,组蛋白H3变得高度乙酰化,但在这些基因上未检测到组蛋白H4乙酰化增加。组蛋白H3的快速乙酰化和TFⅢB,c-Myc,GCN5和TRRAP的启动子装配,随后是polⅢ的募集和转录诱导。组蛋白H3的选择性乙酰化将c-Myc的polⅢ激活与其他系统中观察到的机制区分开。

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