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布氏锥虫活性反式剪接体中存在小U5样RNA的证据。

Evidence for the presence of a small U5-like RNA in active trans-spliceosomes of Trypanosoma brucei.

作者信息

Dungan J M, Watkins K P, Agabian N

机构信息

Intercampus Program in Molecular Parasitology, University of California, San Francisco, 94143-0422, USA.

出版信息

EMBO J. 1996 Aug 1;15(15):4016-29.

Abstract

The existence of the Trypanosoma brucei 5' splice site on a small RNA of uniform sequence (the spliced leader or SL RNA) has allowed us to characterize the RNAs with which it interacts in vivo by psoralen crosslinking treatment. Analysis of the most abundant crosslinks formed by the SL RNA allowed us previously to identify the spliced leader-associated (SLA) RNA. The role of this RNA in trans-splicing, as well as the possible existence of an analogous RNA interaction in cis-splicing, is unknown. We show here that the 5' splice site region of the SL RNA is also crosslinked in vivo to a second small RNA. Although it is very small and lacks a 5' trimethylguanosine (TMG) cap, the SLA2RNA possesses counterparts of the conserved U5 snRNA stem-loop 1 and internal loop 1 sequence elements, as well as a potential trypanosome snRNA core protein binding site; these combined features meet the phylogenetic definition of U5 snRNA. Like U5, the SLA2 RNA forms an RNP complex with the U4 and U6 RNAs, and interacts with the 5' splice site region via its putative loop 1 sequence. In a final analogy with U5, the SLA2 RNA is found crosslinked to a molecule identical to the free 5' exon splicing intermediate. These data present a compelling case for the SLA2 RNA not only as an active trans-spliceosomal component, but also for its identification as the trypanosome U5 structural homolog. The presence of a U5-like RNA in this ancient eukaryote establishes the universality of the spliceosomal RNA core components.

摘要

布氏锥虫5'剪接位点存在于具有一致序列的小RNA(剪接前导序列或SL RNA)上,这使我们能够通过补骨脂素交联处理来表征其在体内相互作用的RNA。对SL RNA形成的最丰富交联的分析使我们先前能够鉴定出与剪接前导序列相关的(SLA)RNA。该RNA在反式剪接中的作用以及在顺式剪接中类似RNA相互作用的可能存在尚不清楚。我们在此表明,SL RNA的5'剪接位点区域在体内也与第二种小RNA交联。尽管SLA2RNA非常小且缺乏5'三甲基鸟苷(TMG)帽,但它具有保守的U5 snRNA茎环1和内环1序列元件的对应物,以及潜在的锥虫snRNA核心蛋白结合位点;这些综合特征符合U5 snRNA的系统发育定义。与U5一样,SLA2 RNA与U4和U6 RNA形成RNP复合物,并通过其假定的环1序列与5'剪接位点区域相互作用。与U5的最后一个相似之处在于,发现SLA2 RNA与一个与游离5'外显子剪接中间体相同的分子交联。这些数据有力地证明了SLA2 RNA不仅是一种活跃的反式剪接体成分,而且还证明了它可被鉴定为锥虫U5结构同源物。在这种古老的真核生物中存在类似U5的RNA,确立了剪接体RNA核心成分的普遍性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f27/452122/afe4b341eeec/emboj00015-0253-a.jpg

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