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首页> 外文期刊>Molecular and Cellular Biology >The Essential N Terminus of the Pta1 Scaffold Protein Is Required for snoRNA Transcription Termination and Ssu72 Function but Is Dispensable for Pre-mRNA 3′-End Processing
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The Essential N Terminus of the Pta1 Scaffold Protein Is Required for snoRNA Transcription Termination and Ssu72 Function but Is Dispensable for Pre-mRNA 3′-End Processing

机译:Pta1支架蛋白的必需N末端是snoRNA转录终止和Ssu72功能所必需的,但对于pre-mRNA 3'-末端加工是必不可少的

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Saccharomyces cerevisiae Pta1 is a component of the cleavage/polyadenylation factor (CPF) 3′-end processing complex and functions in pre-mRNA cleavage, poly(A) addition, and transcription termination. In this study, we investigated the role of the N-terminal region of Pta1 in transcription and processing. We report that a deletion of the first 75 amino acids (pta175) causes thermosensitive growth, while the deletion of an additional 25 amino acids is lethal. The pta175 mutant is defective for snoRNA termination, RNA polymerase II C-terminal domain Ser5-P dephosphorylation, and gene looping but is fully functional for mRNA 3′-end processing. Furthermore, different regions of Pta1 interact with the CPF subunits Ssu72, Pti1, and Ysh1, supporting the idea that Pta1 acts as a scaffold to organize CPF. The first 300 amino acids of Pta1 are sufficient for interactions with Ssu72, which is needed for pre-mRNA cleavage. By the degron-mediated depletion of Pta1, we show that the removal of this essential region leads to a loss of Ssu72, yet surprisingly, in vitro cleavage and polyadenylation remain efficient. In addition, a fragment containing amino acids 1 to 300 suppresses 3′-end processing in wild-type extracts. These findings suggest that the amino terminus of Pta1 has an inhibitory effect and that this effect can be neutralized through the interaction with Ssu72.
机译:酿酒酵母 Pta1是裂解/聚腺苷酸化因子(CPF)3'-末端加工复合物的组成部分,在前mRNA裂解,poly(A)添加和转录终止中起作用。在这项研究中,我们调查了Pta1 N末端区域在转录和加工中的作用。我们报告说,删除前75个氨基酸( pta1 75 )会引起热敏性生长,而删除另外25个氨基酸则是致命的。 pta1 75 突变体在snoRNA终止,RNA聚合酶II C末端结构域Ser5-P磷酸去磷酸化和基因环化方面存在缺陷,但对mRNA 3'-具有完全功能结束处理。此外,Pta1的不同区域与CPF亚基Ssu72,Pti1和Ysh1相互作用,支持Pta1充当组织CPF的支架的想法。 Pta1的前300个氨基酸足以与Ssu72相互作用,这是前mRNA切割所必需的。通过地格隆介导的Pta1耗竭,我们表明该基本区域的去除导致Ssu72的丢失,但令人惊讶的是,体外裂解和聚腺苷酸化仍然有效。另外,含有氨基酸1至300的片段抑制了野生型提取物中的3'末端加工。这些发现表明,Pta1的氨基末端具有抑制作用,并且该作用可以通过与Ssu72的相互作用来中和。

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