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Nrd1 interacts with the nuclear exosome for 3' processing of RNA polymerase II transcripts.

机译:Nrd1与核外泌体相互作用以进行RNA聚合酶II转录本的3'加工。

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The exosome complex is involved in multiple RNA processing and degradation pathways. How exosome is recruited to particular RNA substrates and then chooses between RNA processing and degradation modes remains unclear. We find that the RNA binding protein Nrd1, complexed with its partners Nab3, Sen1, and cap binding complex, physically interacts with the nuclear form of exosome. Nrd1 stimulates the RNA degradation activity of the exosome in vitro. However, Nrd1 can also block 3' to 5' degradation by the exosome at some Nrd1 binding sites. Nrd1 mutations share some phenotypes with exosome mutants, including increased readthrough transcription from several mRNA and sn/snoRNA genes. Therefore, Nrd1 may recruit exosome to RNA and influence the choice between processing and degradation. Since Nrd1 is known to bind RNA polymerase II and be important for sn/snoRNA 3' end processing, Nrd1 may link transcription and RNA 3' end formation with surveillance by the exosome.
机译:外泌体复合物参与多种RNA加工和降解途径。仍然不清楚外泌体如何募集到特定的RNA底物,然后在RNA加工和降解模式之间进行选择。我们发现RNA结合蛋白Nrd1,与其伙伴Nab3,Sen1和帽结合复合物复合,与外泌体的核形式发生物理相互作用。 Nrd1在体外刺激外泌体的RNA降解活性。但是,Nrd1还可以通过外泌体在某些Nrd1结合位点阻止3'至5'降解。 Nrd1突变与外来体突变体共有一些表型,包括来自多个mRNA和sn / snoRNA基因的通读转录增加。因此,Nrd1可能募集外来体到RNA,并影响加工和降解之间的选择。由于已知Nrd1结合RNA聚合酶II,并且对于sn / snoRNA 3'末端加工很重要,因此Nrd1可以将转录和RNA 3'末端形成与外来体的监视联系起来。

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