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真核生物THO/TREX复合物是高效转录延伸所必需的分子证据。

Molecular evidence that the eukaryotic THO/TREX complex is required for efficient transcription elongation.

作者信息

Rondón Ana G, Jimeno Sonia, García-Rubio María, Aguilera Andrés

机构信息

Departamento de Genética, Facultad de Biología, Universidad de Sevilla, Avenida Reina Mercedes 6, 41012 Sevilla, Spain.

出版信息

J Biol Chem. 2003 Oct 3;278(40):39037-43. doi: 10.1074/jbc.M305718200. Epub 2003 Jul 18.

Abstract

THO/TREX is a conserved eukaryotic complex formed by the core THO complex plus proteins involved in mRNA metabolism and export such as Sub2 and Yra1. Mutations in any of the THO/TREX structural genes cause pleiotropic phenotypes such as transcription impairment, increased transcription-associated recombination, and mRNA export defects. To assay the relevance of THO/TREX complex in transcription, we performed in vitro transcription elongation assays in mutant cell extracts using supercoiled DNA templates containing two G-less cassettes. With these assays, we demonstrate that hpr1delta, tho2delta, and mft1delta mutants of the THO complex and sub2 mutants show significant reductions in the efficiency of transcription elongation. The mRNA expression defect of hpr1delta mutants was not due to an increase in mRNA decay, as determined by mRNA half-life measurements and mRNA time course accumulation experiments in the absence of Rrp6p exoribonuclease. This work demonstrates that THO and Sub2 are required for efficient transcription elongation, providing further evidence for the coupling between transcription and mRNA metabolism and export.

摘要

THO/TREX是一种保守的真核生物复合物,由核心THO复合物加上参与mRNA代谢和输出的蛋白质(如Sub2和Yra1)组成。THO/TREX任何结构基因的突变都会导致多效性表型,如转录受损、转录相关重组增加以及mRNA输出缺陷。为了测定THO/TREX复合物在转录中的相关性,我们使用含有两个无G盒的超螺旋DNA模板,在突变细胞提取物中进行了体外转录延伸测定。通过这些测定,我们证明THO复合物的hpr1δ、tho2δ和mft1δ突变体以及sub2突变体在转录延伸效率上有显著降低。hpr1δ突变体的mRNA表达缺陷并非由于mRNA降解增加,这是通过在没有Rrp6p外切核糖核酸酶的情况下进行的mRNA半衰期测量和mRNA时间进程积累实验确定的。这项工作表明THO和Sub2是高效转录延伸所必需的,为转录与mRNA代谢和输出之间的偶联提供了进一步的证据。

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