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Histones are required for transcription of yeast rRNA genes by RNA polymerase I

机译:RNA聚合酶I转录酵母rRNA基因需要组蛋白

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Nucleosomes and their histone components have generally been recognized to act negatively on transcription. However, purified upstream activating factor (UAF), a transcription initiation factor required for RNA polymerase (Pol) I transcription in Saccharomyces cerevisiae, contains histones H3 and H4 and four nonhistone protein subunits. Other studies have shown that histones H3 and H4 are associated with actively transcribed rRNA genes. To examine their functional role in Pol I transcription, we constructed yeast strains in which synthesis of H3 is achieved from the glucose-repressible GAL10 promoter. We found that partial depletion of H3 (≈50% depletion) resulted in a strong inhibition (>80%) of Pol I transcription. A combination of biochemical analysis and electron microscopic (EM) analysis of Miller chromatin spreads indicated that initiation and elongation steps and rRNA processing were compromised upon histone depletion. A clear decrease in relative amounts of UAF, presumably caused by reduced stability, was also observed under the conditions of H3 depletion. Therefore, the observed inhibition of initiation can be explained, in part, by the decrease in UAF concentration. In addition, the EM results suggested that the defects in rRNA transcript elongation and processing may be a result of loss of histones from rRNA genes rather than (or in addition to) an indirect consequence of effects of histone depletion on expression of other genes. Thus, these results show functional importance of histones associated with actively transcribed rRNA genes.
机译:通常已经认识到核小体及其组蛋白成分对转录起负面作用。但是,纯化的上游激活因子(UAF)是酿酒酵母中RNA聚合酶(Pol)I转录所需的转录起始因子,它包含组蛋白H3和H4和四个非组蛋白蛋白质亚基。其他研究表明,组蛋白H3和H4与活跃转录的rRNA基因有关。为了检查其在Pol I转录中的功能,我们构建了酵母菌株,其中可通过葡萄糖可抑制的GAL10启动子合成H3。我们发现H3的部分耗竭(≈50%耗竭)导致对Pol I转录的强烈抑制(> 80%)。米勒染色质散布的生化分析和电子显微镜(EM)分析的组合表明,组蛋白耗尽会损害起始和延伸步骤以及rRNA加工。在H3耗尽的条件下,还观察到UAF相对量的明显下降,这可能是由于稳定性降低所致。因此,观察到的对启动的抑制可以部分通过UAF浓度的降低来解释。另外,EM结果表明rRNA转录物延伸和加工中的缺陷可能是rRNA基因损失组蛋白的结果,而不是(或除了)组蛋白耗竭对其他基因表达的间接影响。因此,这些结果显示了与活性转录的rRNA基因相关的组蛋白的功能重要性。

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