ASSEMBLY OF MITOCHONDRIAL RIBONUCLEOPROTEIN COMPLEXES INVOLVES SPECIFIC GUIDE RNA (GRNA)-BINDING PROTEINS AND GRNA DOMAINS BUT DOES NOT REQUIRE PREEDITED MESSENGER-RNA

被引:60
作者
READ, LK
GORINGER, HU
STUART, K
机构
[1] SEATTLE BIOMED RES INST,4 NICKERSON ST,SEATTLE,WA 98109
[2] UNIV MUNICH,GENZENTRUM,MOLEK BIOL LAB,D-82152 MARTINSRIED,GERMANY
[3] UNIV WASHINGTON,DEPT PATHOBIOL,SEATTLE,WA 98195
关键词
D O I
10.1128/MCB.14.4.2629
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. Goringer, 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.
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页码:2629 / 2639
页数:11
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