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PMID: 12139607 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

RNA editing: complexity and complications.

Molecular microbiology ·Vol. 45 ·No. 3 ·2002-08-00 ·Pages 591-6

Stuart K, Panigrahi AK

Abstract

RNA editing in Trypanosomatids creates functional mitochondrial mRNAs by extensive uridylate (U) insertion and deletion as specified by small guide RNAs (gRNAs). Editing is catalysed by the multiprotein editosome. Over 20 of its protein components have been identified and additional proteins are likely to function in editing and its regulation. The functions of only a few editosome proteins have been determined. Surprisingly, there are related pairs or sets of editosome proteins, and insertion and deletion editing appear to be functionally and perhaps spatially separate. A model for the editosome is proposed, which has a catalysis domain with separate sectors for insertion and deletion editing. It also contains domains for anchor duplex and upstream RNA binding, which position the sequence to be edited in the catalysis domain.

MeSH Terms
Animals RNA Editing/physiology RNA, Protozoan/chemistry,metabolism Trypanosoma brucei brucei/genetics,physiology
Chemicals
RNA, Protozoan
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Stuart Kenneth
Seattle Biomedical Research Institute, WA 98109, USA. [email protected]
Panigrahi Aswini K
Article Info
Journal
Molecular microbiology
Abbr.
Mol Microbiol
ISSN
0950-382X
Published
2002-08-00
Pages
591-6
Language
English
Region
England
NLM ID
8712028
Subset
IM
Grants
NIAID NIH HHS · AI14102 · United States
NIGMS NIH HHS · GM42188 · United States
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