首页> 外文期刊>Genes and Development: a Journal Devoted to the Molecular Analysis of Gene Expression in Eukaryotes, Prokaryotes, and Viruses >The Prp18 protein stabilizes the interaction of both exons with the U5 snRNA during the second step of pre-mRNA splicing.
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The Prp18 protein stabilizes the interaction of both exons with the U5 snRNA during the second step of pre-mRNA splicing.

机译:在mRNA前剪接的第二步中,Prp18蛋白稳定了两个外显子与U5 snRNA的相互作用。

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摘要

Interaction of the ends of the exons with loop 1 of the U5 snRNA aligns the exons for ligation in the second step of pre-mRNA splicing. To study the effect of Prp18 on the exons' interactions, we analyzed the splicing of pre-mRNAs with random sequences in the exon bases at the splice junctions. The exon mutations had large effects on splicing in yeast with a Prp18 protein lacking its most conserved region, but not in wild-type yeast. Analysis of splicing kinetics demonstrated that only the second step was affected in vivo and in vitro, showing that Prp18 - and specifically its conserved region - plays a key role in stabilizing the interaction of the exons with the spliceosome at the time of exon joining. Superior exon sequences defined by the prp18 results accelerated the second step of splicing by wild-type spliceosomes with inefficient AT-AC pre-mRNAs, implying that normal exon interactions follow the rules we discerned for prp18 splicing. Our results show that As are preferred at the ends of both exons and support a revised model of the interactions of the exons with U5 in which the exons are arranged in a continuous double helix that facilitates the second reaction.
机译:外显子末端与U5 snRNA的环1的相互作用使外显子比对,以便在mRNA前剪接的第二步进行连接。为了研究Prp18对外显子相互作用的影响,我们分析了前mRNA的剪接处外显子碱基中具有随机序列的剪接。外显子突变对缺乏最保守区域的Prp18蛋白的酵母的剪接有很大影响,而在野生型酵母中则没有。剪接动力学分析表明,体内和体外仅影响第二步,表明Prp18-特别是其保守区-在稳定外显子连接时外显子与剪接体的相互作用中起关键作用。由prp18定义的优良外显子序列加快了野生型剪接体与低效率AT-AC pre-mRNA剪接的第二步,这意味着正常的外显子相互作用遵循我们为prp18剪接所识别的规则。我们的结果表明,As在两个外显子的末端都是优选的,并支持外显子与U5相互作用的修正模型,其中外显子以连续的双螺旋排列,这有助于第二反应。

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