首页> 美国卫生研究院文献>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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摘要

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 (pta1-Δ75) causes thermosensitive growth, while the deletion of an additional 25 amino acids is lethal. The pta1-Δ75 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是切割/聚腺苷酸化因子(CPF)3'-末端加工复合物的组成部分,在mRNA前切割,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-Δ75)会引起热敏性生长,而删除另外25个氨基酸则是致命的。 pta1-Δ75突变体在snoRNA终止,RNA聚合酶II C末端结构域Ser5-P脱磷酸作用和基因环化方面存在缺陷,但在mRNA 3'末端加工中具有完整功能。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的损失,但令人惊讶的是,体外裂解和聚腺苷酸化仍然有效。此外,含有1至300位氨基酸的片段可抑制野生型提取物中的3'末端加工。这些发现表明,Pta1的氨基末端具有抑制作用,并且可以通过与Ssu72的相互作用来中和该作用。

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