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Functional analysis of the U5 snRNA loop 1 in the second catalytic step of yeast pre-mRNA splicing.

机译:U5 snRNA loop 1在酵母预mRNA剪接的第二个催化步骤中的功能分析。

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摘要

The U5 snRNA loop 1 interacts with the 5' exon before the first step of pre-mRNA splicing and with the 5' and 3' exons following the first step. These U5-exon interactions are proposed to hold the exons in the correct orientation for the second step of splicing. Reconstitution of U5 snRNPs in vitro indicated that U5 loop 1-5' exon interactions are not necessary for the first catalytic step of splicing but are critical for the second step in yeast spliceosomes. We systematically made deletion and insertion mutations in loop 1 then monitored splicing activity and loop-exon interactions by cross-linking. Single nucleotide deletions or insertions in loop 1 permitted both steps of splicing. Larger insertions or deletions allowed the first step but progressively inhibited the second step. Analysis of selected loop 1 insertions and deletions by cross-linking revealed that inhibition of the second catalytic step resulted from misalignment of the 5' and 3' exons. These data indicate that the size of loop 1 is critical for proper alignment of the exons for the second catalytic step of splicing and that the 3' exon is positioned on loop 1 independently of the 5' exon.
机译:U5 snRNA环1在mRNA前剪接的第一步之前与5'外显子相互作用,而在第一步之后与5'和3'外显子相互作用。建议这些U5-外显子相互作用将外显子保持在正确的方向,以便进行第二步拼接。 U5 snRNPs的体外重组表明,U5环1-5'外显子相互作用对于剪接的第一步催化步骤不是必需的,但对于酵母剪接体的第二步至关重要。我们系统地在环1中进行了缺失和插入突变,然后通过交联监控了剪接活性和环-外显子相互作用。环1中单核苷酸的缺失或插入允许两个剪接步骤。较大的插入或删除允许第一步,但逐渐抑制了第二步。通过交联对所选环1插入和缺失的分析表明,第二催化步骤的抑制是由5'和3'外显子的未对准引起的。这些数据表明,环1的大小对于用于剪接的第二催化步骤的外显子的正确排列至关重要,并且3'外显子独立于5'外显子而位于环1上。

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