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线粒体核糖核蛋白复合体的组装涉及特定的指导RNA(gRNA)结合蛋白和gRNA结构域,但不需要经过编辑前的mRNA。

Assembly of mitochondrial ribonucleoprotein complexes involves specific guide RNA (gRNA)-binding proteins and gRNA domains but does not require preedited mRNA.

作者信息

Read L K, Göringer H U, Stuart K

机构信息

Seattle Biomedical Research Institute, Washington 98109-1651.

出版信息

Mol Cell Biol. 1994 Apr;14(4):2629-39. doi: 10.1128/mcb.14.4.2629-2639.1994.

DOI:10.1128/mcb.14.4.2629-2639.1994
PMID:8139563
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC358630/
Abstract

RNA editing in kinetoplastids probably employs a macromolecular complex, the editosome, that is likely to include the guide RNAs (gRNAs) which specify the edited sequence. Specific ribonucleoprotein (RNP) complexes which form in vitro with gRNAs (H. U. Göringer, D. J. Koslowsky, T. H. Morales, and K. D. Stuart, Proc. Natl. Acad. Sci. USA, in press) are potential editosomes or their precursors. We find that several factors are important for in vitro formation of these RNP complexes and identify specific gRNA-binding proteins present in the complexes. Preedited mRNA promotes the in vitro formation of the four major gRNA-containing RNP complexes under some conditions but is required for the formation of only a subcomponent of one complex. The 5' gRNA sequence encompassing the RYAYA and anchor regions and the 3' gRNA oligo(U) tail are both important in complex formation, since their deletion results in a dramatic decrease of some complexes and the absence of others. UV cross-linking experiments identify several proteins which are in contact with gRNA and preedited mRNA in mitochondrial extracts. Proteins of 25 and 90 kDa are highly specific for gRNAs, and the 90-kDa protein binds specifically to gRNA oligo(U) tails. The gRNA-binding proteins exhibit a differential distribution between the four in vitro-formed complexes. These experiments reveal several proteins potentially involved in RNA editing and indicate that multiple recognition elements in gRNAs are used for complex formation.

摘要

动质体中的RNA编辑可能利用一种大分子复合物——编辑体,它可能包含指定编辑序列的引导RNA(gRNA)。在体外与gRNA形成的特定核糖核蛋白(RNP)复合物(H. U. 戈林格、D. J. 科斯洛夫斯基、T. H. 莫拉莱斯和K. D. 斯图尔特,《美国国家科学院院刊》,即将发表)是潜在的编辑体或其前体。我们发现几个因素对这些RNP复合物的体外形成很重要,并鉴定出复合物中存在的特定gRNA结合蛋白。在某些条件下,预编辑的mRNA促进了四种主要含gRNA的RNP复合物的体外形成,但仅对其中一种复合物的一个亚组分的形成是必需的。包含RYAYA和锚定区域的5' gRNA序列以及3' gRNA寡聚(U)尾在复合物形成中都很重要,因为它们的缺失会导致一些复合物显著减少,而其他复合物则不存在。紫外线交联实验鉴定出线粒体提取物中与gRNA和预编辑的mRNA接触的几种蛋白质。25 kDa和90 kDa的蛋白质对gRNA具有高度特异性,并且90 kDa的蛋白质特异性结合gRNA寡聚(U)尾。gRNA结合蛋白在四种体外形成的复合物之间表现出差异分布。这些实验揭示了几种可能参与RNA编辑的蛋白质,并表明gRNA中的多个识别元件用于复合物形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cdf/358630/754923f5821f/molcellb00004-0426-a.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cdf/358630/c573cfe53d50/molcellb00004-0425-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cdf/358630/713226319aa6/molcellb00004-0425-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cdf/358630/754923f5821f/molcellb00004-0426-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cdf/358630/750f90588dc0/molcellb00004-0419-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cdf/358630/802400f43a67/molcellb00004-0420-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cdf/358630/a088d2a71936/molcellb00004-0420-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cdf/358630/485542e4afd3/molcellb00004-0421-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cdf/358630/d8f782d731a3/molcellb00004-0422-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cdf/358630/f6d1caeaf13f/molcellb00004-0423-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cdf/358630/fa1349031bcc/molcellb00004-0424-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cdf/358630/c573cfe53d50/molcellb00004-0425-a.jpg
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