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在纤细短膜虫线粒体提取物中,引导RNA的U尾作为引导RNA-信使RNA嵌合体形成中特异性决定因素的一种可能作用。

A possible role for the guide RNA U-tail as a specificity determinant in formation of guide RNA-messenger RNA chimeras in mitochondrial extracts of Crithidia fasciculata.

作者信息

Arts G J, Sloof P, Benne R

机构信息

E.C. Slater Institute, University of Amsterdam, Academic Medical Centre, The Netherlands.

出版信息

Mol Biochem Parasitol. 1995 Jul;73(1-2):211-22. doi: 10.1016/0166-6851(95)00119-l.

DOI:10.1016/0166-6851(95)00119-l
PMID:8577329
Abstract

Chimeric g(uide) RNA:pre-mRNA molecules are potential intermediates of the RNA editing process in kinetoplastid mitochondria. We have studied the characteristics of chimeric molecules formed in mitochondrial extracts of the insect trypanosomatid Crithidia fasciculata which had been supplied with synthetic NADH dehydrogenase (ND) subunit-7 gRNA and pre-mRNA variants. The ability of a gRNA to participate in chimera formation in this system depends on the possibility of base pairing with the pre-mRNA via the anchor sequence, but not on the presence of a U-tail or a full-length informational part. Chimeras formed with a specific gRNA:pre-mRNA pair displayed a large variation in length, due to variably sized 3' end truncations of the gRNA moieties and variation in the sites in the pre-mRNA to which the gRNAs were attached. Surprisingly, the presence of a U-tail in the gRNA for a large part determined the specificity of the linkage. In 60% of the cases gRNAs possessing a U-tail of at least one residue were attached to an editing site, whereas 75% of the gRNAs without Us were attached to non-editing sites. Furthermore, the chimera forming activity was greatly stimulated by the addition of ATP but not by AMP-CPP, an ATP-analogue with a non-hydrolyzable alpha-beta phosphate bond. This suggests the involvement in the chimera formation of an RNA ligase.

摘要

嵌合g(uide)RNA:前体mRNA分子是动基体线粒体中RNA编辑过程的潜在中间体。我们研究了在已提供合成烟酰胺腺嘌呤二核苷酸脱氢酶(ND)亚基7 gRNA和前体mRNA变体的昆虫锥虫克氏锥虫线粒体提取物中形成的嵌合分子的特性。在该系统中,gRNA参与嵌合体形成的能力取决于通过锚定序列与前体mRNA碱基配对的可能性,而不取决于U尾或全长信息部分的存在。由特定gRNA:前体mRNA对形成的嵌合体在长度上表现出很大差异,这是由于gRNA部分3'端截短大小可变以及gRNA连接到前体mRNA的位点不同所致。令人惊讶的是,gRNA中U尾的存在在很大程度上决定了连接的特异性。在60%的情况下,具有至少一个残基U尾的gRNA连接到编辑位点,而75%没有U的gRNA连接到非编辑位点。此外,添加ATP可极大地刺激嵌合体形成活性,但添加AMP-CPP(一种具有不可水解α-β磷酸键的ATP类似物)则不会。这表明RNA连接酶参与了嵌合体的形成。

相似文献

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A possible role for the guide RNA U-tail as a specificity determinant in formation of guide RNA-messenger RNA chimeras in mitochondrial extracts of Crithidia fasciculata.在纤细短膜虫线粒体提取物中,引导RNA的U尾作为引导RNA-信使RNA嵌合体形成中特异性决定因素的一种可能作用。
Mol Biochem Parasitol. 1995 Jul;73(1-2):211-22. doi: 10.1016/0166-6851(95)00119-l.
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RNA editing: a mechanism for gRNA-specified uridylate insertion into precursor mRNA.RNA编辑:一种将gRNA指定的尿苷酸插入前体mRNA的机制。
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Implications of novel guide RNA features for the mechanism of RNA editing in Crithidia fasciculata.新型向导RNA特征对纤细短膜虫RNA编辑机制的影响
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Guide RNA-mRNA chimeras, which are potential RNA editing intermediates, are formed by endonuclease and RNA ligase in a trypanosome mitochondrial extract.向导RNA-信使核糖核酸嵌合体是潜在的RNA编辑中间体,由锥虫线粒体提取物中的核酸内切酶和RNA连接酶形成。
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The 5'-terminal region of the apocytochrome b transcript in Crithidia fasciculata is successively edited by two guide RNAs in the 3' to 5' direction.在纤细短膜虫中,脱辅基细胞色素b转录本的5'末端区域在3'到5'方向上先后被两个引导RNA编辑。
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Formation of guide RNA/messenger RNA chimeric molecules in vitro, the initial step of RNA editing, is dependent on an anchor sequence.体外向导RNA/信使RNA嵌合分子的形成是RNA编辑的起始步骤,该过程依赖于一个锚定序列。
Proc Natl Acad Sci U S A. 1992 Dec 15;89(24):11944-8. doi: 10.1073/pnas.89.24.11944.
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Native mRNA editing complexes from Trypanosoma brucei mitochondria.来自布氏锥虫线粒体的天然信使核糖核酸编辑复合体。
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Trypanosome U-deletional RNA editing involves guide RNA-directed endonuclease cleavage, terminal U exonuclease, and RNA ligase activities.锥虫U缺失型RNA编辑涉及引导RNA指导的内切核酸酶切割、末端U核酸外切酶和RNA连接酶活性。
Proc Natl Acad Sci U S A. 1996 Aug 20;93(17):8901-6. doi: 10.1073/pnas.93.17.8901.

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RNA editing in kinetoplastid protozoa.动质体原生动物中的RNA编辑。
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