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来自单基因锥虫Leptomonas collosoma的反式剪接体U4 RNA。控制其表达的转录tRNA样元件的克隆与鉴定。

The trans-spliceosomal U4 RNA from the monogenetic trypanosomatid Leptomonas collosoma. Cloning and identification of a transcribed trna-like element that controls its expression.

作者信息

Li L, Otake L R, Xu Y x, Michaeli S

机构信息

Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan 52900, Israel.

出版信息

J Biol Chem. 2000 Jan 28;275(4):2259-64. doi: 10.1074/jbc.275.4.2259.

Abstract

U4 small nuclear RNA is essential for trans-splicing. Here we report the cloning of U4 snRNA gene from Leptomonas collosoma and analysis of elements controlling its expression. The trypanosome U4 RNA is the smallest known, it carries an Sm-like site, and has the potential for extensive intermolecular base pairing with the U6 RNA. Sequence analysis of the U4 locus indicates the presence of a tRNA-like element 86 base pairs upstream of the gene that is divergently transcribed to yield a stable small tRNA-like RNA. Two additional tRNA genes, tRNA(Pro) and tRNA(Gly), were found upstream of this element. By stable expression of a tagged U4 RNA, we demonstrate that the tRNA-like gene, but not the upstream tRNA genes, is essential for U4 expression and that the B box but not the A Box of the tRNA-like gene is crucial for expression in vivo. Mapping the 2'-O-methyl groups on U4 and U6 small nuclear RNAs suggests the presence of modifications in canonical positions. However, the number of modified nucleotides is fewer than in mammalian homologues. The U4 genomic organization including both tRNA-like and tRNA genes may represent a relic whereby trypanosomatids "hired" tRNA genes to provide extragenic promoter elements. The close proximity of tRNA genes to the tRNA-like molecule in the U4 locus further suggests that the tRNA-like gene may have evolved from a tRNA member of this cluster.

摘要

U4小核RNA对于反式剪接至关重要。在此我们报道了从粗粘细滴虫中克隆U4 snRNA基因并分析控制其表达的元件。锥虫U4 RNA是已知最小的,它带有一个类Sm位点,并且有可能与U6 RNA广泛进行分子间碱基配对。U4基因座的序列分析表明,在该基因上游86个碱基对处存在一个类似tRNA的元件,它以相反方向转录产生一种稳定的小tRNA样RNA。在这个元件上游还发现了另外两个tRNA基因,即tRNA(Pro)和tRNA(Gly)。通过稳定表达带标签的U4 RNA,我们证明类似tRNA的基因而非上游tRNA基因对于U4表达至关重要,并且类似tRNA基因的B框而非A框对于体内表达至关重要。对U4和U6小核RNA上的2'-O-甲基基团进行定位表明在典型位置存在修饰。然而,修饰核苷酸的数量比哺乳动物同源物中的少。包括类似tRNA和tRNA基因的U4基因组组织可能代表一种遗迹,即锥虫“征用”tRNA基因来提供基因外启动子元件。U4基因座中tRNA基因与类似tRNA分子的紧密相邻进一步表明类似tRNA的基因可能是从该簇的一个tRNA成员进化而来。

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