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论共转录的重要性。

On the importance of being co-transcriptional.

作者信息

Neugebauer Karla M

机构信息

Max Planck Institute for Molecular Cell Biology and Genetics, Pfotenhauerstrasse 108, 01307 Dresden, Germany.

出版信息

J Cell Sci. 2002 Oct 15;115(Pt 20):3865-71. doi: 10.1242/jcs.00073.

Abstract

Intense research in recent years has shown that many pre-mRNA processing events are co-transcriptional or at least begin during RNA synthesis by RNA polymerase II (Pol II). But is it important that pre-mRNA processing occurs co-transcriptionally? Whereas Pol II directs 5' capping of mRNA by binding to and recruiting all three capping activities to transcription units, co-transcriptional splicing is not obligatory. In some cases, such as alternative splicing, splicing may occur post-transcriptionally owing to the slower kinetics of splicing unfavorable introns. Despite recent models in which splicing factors are bound directly to the C-terminal domain (CTD) of Pol II, little evidence supports that view. Instead, interactions between snRNPs and transcription elongation factors provide the strongest molecular evidence for a physical link between transcription and splicing. Transcription termination depends on polyadenylation signals, but, like splicing, polyadenylation per se probably begins co-transcriptionally and continues post-transcriptionally. Nascent RNA plays an important role in determining which transcripts are polyadenylated and which alternative terminal exon is used. A recent addition to co-transcriptional RNA processing is a possible RNA surveillance step prior to release of the mRNP from the transcription unit, which appears to coordinate nuclear transport with mRNA processing and may be mediated by components of the nuclear exosome.

摘要

近年来的深入研究表明,许多前体mRNA加工事件是共转录的,或者至少在RNA聚合酶II(Pol II)进行RNA合成期间就开始了。但是前体mRNA加工共转录发生很重要吗?虽然Pol II通过与转录单元结合并招募所有三种加帽活性来指导mRNA的5'端加帽,但共转录剪接并非必需。在某些情况下,如可变剪接,由于不利内含子剪接的动力学较慢,剪接可能在转录后发生。尽管最近有模型认为剪接因子直接与Pol II的C端结构域(CTD)结合,但几乎没有证据支持这一观点。相反,核小核糖核蛋白(snRNP)与转录延伸因子之间的相互作用为转录和剪接之间的物理联系提供了最有力的分子证据。转录终止取决于聚腺苷酸化信号,但是,与剪接一样,聚腺苷酸化本身可能在共转录时开始,并在转录后继续。新生RNA在决定哪些转录本进行聚腺苷酸化以及使用哪个可变末端外显子方面起着重要作用。共转录RNA加工的一个最新进展是,在mRNP从转录单元释放之前可能存在一个RNA监测步骤,这似乎将核转运与mRNA加工协调起来,并且可能由核外泌体的成分介导。

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