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ATP-dependent interaction of yeast U5 snRNA loop 1 with the 5' splice site.

机译:酵母U5 snRNA环1与5'剪接位点的ATP依赖性相互作用。

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摘要

Pre-messenger RNA splicing is a two-step process by which introns are removed and exons joined together. In yeast, the U5 snRNA loop 1 interacts with the 5' exon before the first step of splicing and with the 5' and 3' exons before the second step. In vitro studies revealed that yeast U5 loop 1 is not required for the first step of splicing but is essential for holding the 5' and 3' exons for ligation during the second step. It is critical, therefore, that loop 1 contacts the 5' exon before the first step of splicing to hold this exon following cleavage from the pre-mRNA. At present it is not known how U5 loop 1 is positioned on the 5' exon prior to the first step of splicing. To address this question, we have used site-specific photoactivated crosslinking in yeast spliceosomes to investigate the interaction of U5 loop 1 with the pre-mRNA prior to the first step of splicing. We have found that the highly conserved uridines in loop 1 make ATP-dependent contacts with an approximately 8-nt region at the 5' splice site that includes the invariant GU. These interactions are dependent on functional U2 and U6 snRNAs. Our results support a model where U5 snRNA loop 1 interacts with the 5' exon in two steps during its targeting to the 5' splice site.
机译:信使前RNA剪接是一个两步过程,通过该过程可以去除内含子并将外显子连接在一起。在酵母中,U5 snRNA环1在第一步剪接之前与5'外显子相互作用,在第二步之前与5'和3'外显子相互作用。体外研究表明,第一步剪接不需要酵母U5环1,但对于第二步保持5'和3'外显子进行连接至关重要。因此,至关重要的是,在进行剪接的第一步之前,环1必须与5'外显子接触,以在从前mRNA切割下来后保持该外显子。目前尚不知道在第一步剪接之前如何将U5环1定位在5'外显子上。为了解决这个问题,我们在酵母剪接体中使用了位点特异性的光活化交联来研究在第一步剪接之前,U5 loop 1与pre-mRNA的相互作用。我们已经发现,环1中高度保守的尿苷与包括不变的GU在内的5'剪接位点处的大约8-nt区域形成ATP依赖性接触。这些相互作用取决于功能性U2和U6 snRNA。我们的结果支持了一个模型,其中U5 snRNA环1在靶向5'剪接位点的过程中分两个步骤与5'外显子相互作用。

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