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首页> 外文期刊>Molecular and Cellular Biology >Uridylate Addition and RNA Ligation Contribute to the Specificity of Kinetoplastid Insertion RNA Editing
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Uridylate Addition and RNA Ligation Contribute to the Specificity of Kinetoplastid Insertion RNA Editing

机译:Uridylate添加和RNA连接有助于动素体插入RNA编辑的特异性。

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摘要

RNA editing in Trypanosoma brucei inserts and deletes uridylates (U's) in mitochondrial pre-mRNAs under the direction of guide RNAs (gRNAs). We report here the development of a novel in vitro precleaved editing assay and its use to study the gRNA specificity of the U addition and RNA ligation steps in insertion RNA editing. The 5′ fragment of substrate RNA accumulated with the number of added U's specified by gRNA, and U addition products with more than the specified number of U's were rare. U addition up to the number specified occurred in the absence of ligation, but accumulation of U addition products was slowed. The 5′ fragments with the correct number of added U's were preferentially ligated, apparently by adenylylated RNA ligase since exogenously added ATP was not required and since ligation was eliminated by treatment with pyrophosphate. gRNA-specified U addition was apparent in the absence of ligation when the pre-mRNA immediately upstream of the editing site was single stranded and more so when it was base paired with gRNA. These results suggest that both the U addition and RNA ligation steps contributed to the precision of RNA editing.
机译:在y> Trypanosoma brucei 中的RNA编辑可在指导RNA(gRNA)的指导下插入和删除线粒体前mRNA中的尿苷(U)。我们在这里报告了一种新型的体外预切割编辑测定法的开发及其在研究插入的RNA编辑中U添加的gRNA特异性和RNA连接步骤中的用途。底物RNA的5'片段积累有由gRNA指定的添加U数量,而U添加数量超过指定数量的U添加产物很少。在没有连接的情况下,U的添加达到指定的数量,但是U的添加产物的积累变慢了。由于不需要外源添加的ATP,并且由于通过焦磷酸盐处理消除了连接,因此显然通过腺苷酸化的RNA连接酶优先连接了具有正确数量的U's的5'片段。当紧邻编辑位点上游的pre-mRNA是单链时,在没有连接的情况下,gRNA特定的U添加是明显的,当与gRNA碱基配对时,尤为如此。这些结果表明U添加和RNA连接步骤均有助于RNA编辑的精度。

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