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克氏锥虫和西氏利什曼原虫的反式剪接体U6 RNA:偏离保守的ACAGAG序列以及与剪接前导RNA的潜在碱基配对

trans-spliceosomal U6 RNAs of Crithidia fasciculata and Leptomonas seymouri: deviation from the conserved ACAGAG sequence and potential base pairing with spliced leader RNA.

作者信息

Xu G L, Wieland B, Bindereif A

机构信息

Max-Planck-Institut für Molekulare Genetik, Otto-Warburg-Laboratorium, Berlin (Dahlem), Germany.

出版信息

Mol Cell Biol. 1994 Jul;14(7):4565-70. doi: 10.1128/mcb.14.7.4565-4570.1994.

DOI:10.1128/mcb.14.7.4565-4570.1994
PMID:8007960
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC358828/
Abstract

U6 RNA genes from the trypanosomatids Crithidia fasciculata and Leptomonas seymouri have been isolated and sequenced. As in Trypanosoma brucei, the U6 RNA genes in both C. fasciculata and L. seymouri are arranged in close linkage with upstream tRNA genes. The U6 RNA sequences from C. fasciculata and L. seymouri deviate in five and three positions, respectively, from the published T. brucei sequence. Interestingly, both C. fasciculata U6 RNA genes carry a C-->T change at the second position of the ACAGAG hexanucleotide sequence, which is important for splicing function and has been considered phylogenetically invariable. A compensatory base change of the C. fasciculata spliced leader RNA at the highly conserved 5' splice site position +5, G-->A, suggests that an interaction between the 5' splice site region and U6 RNA recently proposed for the yeast cis-splicing system may also occur in trans splicing.

摘要

已经分离并测序了来自锥虫科的克氏锥虫和西氏利什曼原虫的U6 RNA基因。与布氏锥虫一样,克氏锥虫和西氏利什曼原虫中的U6 RNA基因都与上游tRNA基因紧密连锁排列。克氏锥虫和西氏利什曼原虫的U6 RNA序列分别与已发表的布氏锥虫序列在五个和三个位置上存在差异。有趣的是,克氏锥虫的两个U6 RNA基因在ACAGAG六核苷酸序列的第二个位置都发生了C→T变化,这对剪接功能很重要,并且在系统发育上被认为是不变的。克氏锥虫剪接前导RNA在高度保守的5'剪接位点位置+5处发生的G→A补偿性碱基变化表明,最近在酵母顺式剪接系统中提出的5'剪接位点区域与U6 RNA之间的相互作用也可能发生在反式剪接中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed96/358828/e2354eab1ba3/molcellb00007-0244-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed96/358828/5c90d3d14cee/molcellb00007-0242-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed96/358828/e2354eab1ba3/molcellb00007-0244-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed96/358828/5c90d3d14cee/molcellb00007-0242-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed96/358828/e2354eab1ba3/molcellb00007-0244-a.jpg

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trans-spliceosomal U6 RNAs of Crithidia fasciculata and Leptomonas seymouri: deviation from the conserved ACAGAG sequence and potential base pairing with spliced leader RNA.克氏锥虫和西氏利什曼原虫的反式剪接体U6 RNA:偏离保守的ACAGAG序列以及与剪接前导RNA的潜在碱基配对
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本文引用的文献

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The trans-spliceosomal U2 snRNP protein 40K of Trypanosoma brucei: cloning and analysis of functional domains reveals homology to a mammalian snRNP protein.布氏锥虫的跨剪接体U2小核核糖核蛋白40K:功能域的克隆与分析揭示其与哺乳动物小核核糖核蛋白的同源性
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In vivo structural analysis of spliced leader RNAs in Trypanosoma brucei and Leptomonas collosoma: a flexible structure that is independent of cap4 methylations.布氏锥虫和粗线细滴虫中剪接前导RNA的体内结构分析:一种独立于帽4甲基化的灵活结构。
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Conformational changes of U6 RNA during the spliceosome cycle: an intramolecular helix is essential both for initiating the U4-U6 interaction and for the first step of slicing.剪接体循环过程中U6 RNA的构象变化:一个分子内螺旋对于启动U4-U6相互作用以及剪接的第一步至关重要。
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Functional reconstitution of U6 snRNA in nematode cis- and trans-splicing: U6 can serve as both a branch acceptor and a 5' exon.线虫顺式和反式剪接中U6 snRNA的功能重建:U6既可以作为分支受体,也可以作为5'外显子。
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