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Mechanisms of fidelity in pre-mRNA splicing.

机译:mRNA前剪接中的保真机制。

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摘要

The pre-mRNA splicing machinery consists of five small nuclear RNAs (U1, U2, U4, U5 and U6) and more than fifty proteins. Over the past year, important advances have been made in understanding how these factors function to achieve fidelity in splicing. Of particular note were the discoveries that the splicing factor U2AF(35) recognizes the AG dinucleotide at the 3' splice site early in spliceosome assembly, that a DEAD-box ATPase, Prp28, triggers specific rearrangements of the spliceosome, and that the splicing factor hSlu7 functions in the fidelity of AG choice during catalytic step II of splicing.
机译:mRNA之前的剪接机制由五个小核RNA(U1,U2,U4,U5和U6)和五十多个蛋白质组成。在过去的一年中,在理解这些因素如何发挥作用以实现保真度方面取得了重要进展。特别值得注意的发现是,剪接因子U2AF(35)在剪接体组装的早期识别了3'剪接位点的AG二核苷酸,DEAD-box ATPase Prp28触发了剪接体的特定重排,并且剪接因子hSlu7在剪接的催化步骤II中发挥AG选择的保真作用。

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