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Functional interactions between the transcription and mRNA 3′ end processing machineries mediated by Ssu72 and Sub1

机译:Ssu72和Sub1介导的转录与mRNA 3末端加工机器之间的功能相互作用

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摘要

Transcription and processing of pre-mRNA are coupled events. By using a combination of biochemical, molecular, and genetic methods, we have found that the phylogenetically conserved transcription factor Ssu72 is a component of the cleavage/polyadenylation factor (CPF) of Saccharomyces cerevisiae. Our results demonstrate that Ssu72 is required for 3′ end cleavage of pre-mRNA but is dispensable for poly(A) addition and RNAP II termination. The in vitro cleavage defect caused by depletion of Ssu72 from cells can be rescued by addition of recombinant Ssu72. Ssu72 interacts physically and genetically with the Pta1 subunit of CPF. Overexpression of PTA1 causes synthetic lethality in an ssu72-3 mutant. Moreover, Sub1, which has been implicated in transcription initiation and termination, also interacts with Pta1, and overexpression of SUB1 suppresses the growth and processing defect of a pta1 mutation. Physical interactions of Ssu72 and Sub1 with Pta1 are mutually exclusive. Based on the interactions of Ssu72 and Sub1 with both the Pta1 of CPF and the TFIIB component of the initiation complex, we present a model describing how these novel connections between the transcription and 3′ end processing machineries might facilitate transitions in the RNAP II transcription cycle.
机译:前mRNA的转录和加工是偶发事件。通过结合使用生物化学,分子和遗传方法,我们发现系统发育上保守的转录因子Ssu72是酿酒酵母的裂解/聚腺苷酸化因子(CPF)的组成部分。我们的结果表明,Ssu72是pre-mRNA 3'末端切割所必需的,但对于poly(A)添加和RNAP II终止是必不可少的。可以通过添加重组Ssu72来挽救由细胞中Ssu72耗尽引起的体外切割缺陷。 Ssu72与CPF的Pta1亚基发生物理和遗传相互作用。 PTA1的过表达导致ssu72-3突变体的合成致死性。此外,已参与转录起始和终止的Sub1也与Pta1相互作用,SUB1的过表达抑制了pta1突变的生长和加工缺陷。 Ssu72和Sub1与Pta1的物理相互作用是互斥的。基于Ssu72和Sub1与CPF的Pta1和起始复合物的TFIIB组分的相互作用,我们提出了一个模型,描述了转录和3'末端加工机械之间的这些新颖连接如何促进RNAP II转录周期的过渡。

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