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RNA聚合酶II转录的电子显微镜观察:下游终止需要聚腺苷酸化信号,但不需要转录本切割。

EM visualization of transcription by RNA polymerase II: downstream termination requires a poly(A) signal but not transcript cleavage.

作者信息

Osheim Y N, Proudfoot N J, Beyer A L

机构信息

University of Virginia Health Sciences Center, Department of Microbiology, Charlottesville 22908, USA.

出版信息

Mol Cell. 1999 Mar;3(3):379-87. doi: 10.1016/s1097-2765(00)80465-7.

Abstract

We have used EM visualization of active genes on plasmid vectors in Xenopus oocyte nuclei to investigate the relationship between poly(A) signals and RNA polymerase II transcription termination. Although a functional poly(A) signal is required for efficient termination, cotranscriptional RNA cleavage at the poly(A) site is not. Furthermore, the phenomena of termination and cotranscriptional RNA cleavage can be uncoupled, and the efficiency of both varies independently on different copies of the same plasmid template in the same oocyte nucleus. The combined observations are consistent with a scenario in which there is template-specific addition to Pol II (presumably at the promoter) of elongation and/or RNA processing factors, which are altered upon passage through a poly(A) signal, resulting in termination and, in some cases, cotranscriptional RNA cleavage.

摘要

我们利用电子显微镜对非洲爪蟾卵母细胞核中质粒载体上的活性基因进行可视化,以研究聚腺苷酸化信号与RNA聚合酶II转录终止之间的关系。虽然有效的终止需要功能性聚腺苷酸化信号,但在聚腺苷酸化位点的共转录RNA切割并非如此。此外,终止和共转录RNA切割现象可以解偶联,并且在同一卵母细胞核中同一质粒模板的不同拷贝上,两者的效率独立变化。这些综合观察结果与一种情况相符,即存在向Pol II(可能在启动子处)特异性添加延伸和/或RNA加工因子的模板,这些因子在通过聚腺苷酸化信号时会发生改变,从而导致终止,在某些情况下还会导致共转录RNA切割。

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