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Rtf1是Paf1复合物的一个多功能组分,它通过指导共转录组蛋白修饰来调节基因表达。

Rtf1 is a multifunctional component of the Paf1 complex that regulates gene expression by directing cotranscriptional histone modification.

作者信息

Warner Marcie H, Roinick Kelli L, Arndt Karen M

机构信息

Department of Biological Sciences, University of Pittsburgh, 269 Crawford Hall, 4249 Fifth Avenue, Pittsburgh, PA 15260, USA.

出版信息

Mol Cell Biol. 2007 Sep;27(17):6103-15. doi: 10.1128/MCB.00772-07. Epub 2007 Jun 18.

Abstract

Numerous transcription accessory proteins cause alterations in chromatin structure that promote the progression of RNA polymerase II (Pol II) along open reading frames (ORFs). The Saccharomyces cerevisiae Paf1 complex colocalizes with actively transcribing Pol II and orchestrates modifications to the chromatin template during transcription elongation. To better understand the function of the Rtf1 subunit of the Paf1 complex, we created a series of sequential deletions along the length of the protein. Genetic and biochemical assays were performed on these mutants to identify residues required for the various activities of Rtf1. Our results establish that discrete nonoverlapping segments of Rtf1 are necessary for interaction with the ATP-dependent chromatin-remodeling protein Chd1, promoting covalent modification of histones H2B and H3, recruitment to active ORFs, and association with other Paf1 complex subunits. We observed transcription-related defects when regions of Rtf1 that mediate histone modification or association with active genes were deleted, but disruption of the physical association between Rtf1 and other Paf1 complex subunits caused only subtle mutant phenotypes. Together, our results indicate that Rtf1 influences transcription and chromatin structure through several independent functional domains and that Rtf1 may function independently of its association with other members of the Paf1 complex.

摘要

许多转录辅助蛋白会引起染色质结构的改变,从而促进RNA聚合酶II(Pol II)沿着开放阅读框(ORF)前进。酿酒酵母Paf1复合物与活跃转录的Pol II共定位,并在转录延伸过程中协调对染色质模板的修饰。为了更好地理解Paf1复合物的Rtf1亚基的功能,我们沿着该蛋白质的长度创建了一系列连续缺失。对这些突变体进行了遗传和生化分析,以确定Rtf1各种活性所需的残基。我们的结果表明,Rtf1离散的非重叠片段对于与ATP依赖性染色质重塑蛋白Chd1相互作用、促进组蛋白H2B和H3的共价修饰、募集到活跃的ORF以及与其他Paf1复合物亚基结合是必需的。当Rtf1中介导组蛋白修饰或与活跃基因结合的区域被删除时,我们观察到了与转录相关的缺陷,但Rtf1与其他Paf1复合物亚基之间物理结合的破坏仅导致了轻微的突变表型。总之,我们的结果表明,Rtf1通过几个独立的功能域影响转录和染色质结构,并且Rtf1可能独立于其与Paf1复合物其他成员的结合而发挥作用。

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