RNA interference analyses suggest a transcript-specific regulatory role for mitochondrial RNA-binding proteins MRP1 and MRP2 in RNA editing and other RNA processing in Trypanosoma brucei
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.
Grant support
AI14102
NIAID NIH HHS - United States
PubMed
15504736
DOI
10.1074/jbc.m405933200
PII: S0021-9258(20)76285-X
Knihovny.cz E-resources
- MeSH
- Time Factors MeSH
- DNA Primers chemistry MeSH
- RNA Editing MeSH
- Glycerol chemistry MeSH
- Immunoprecipitation MeSH
- Cloning, Molecular MeSH
- RNA, Messenger metabolism MeSH
- Mitochondrial Proteins metabolism physiology MeSH
- Blotting, Northern MeSH
- Plasmids metabolism MeSH
- RNA-Binding Proteins metabolism physiology MeSH
- Protozoan Proteins metabolism physiology MeSH
- RNA Interference * MeSH
- RNA, Protozoan MeSH
- RNA, Ribosomal metabolism MeSH
- RNA chemistry metabolism MeSH
- Blotting, Southern MeSH
- Transfection MeSH
- Trypanosoma brucei brucei metabolism MeSH
- Protein Binding MeSH
- Blotting, Western MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, U.S. Gov't, P.H.S. MeSH
- Names of Substances
- DNA Primers MeSH
- gBP21 protein, Trypanosoma brucei MeSH Browser
- gBP25 protein, Trypanosoma brucei MeSH Browser
- Glycerol MeSH
- RNA, Messenger MeSH
- Mitochondrial Proteins MeSH
- RNA-Binding Proteins MeSH
- Protozoan Proteins MeSH
- RNA, Protozoan MeSH
- RNA, Ribosomal MeSH
- RNA, ribosomal, 12S MeSH Browser
- RNA MeSH
Mitochondrial RNA-binding proteins MRP1 and MRP2 occur in a heteromeric complex that appears to play a role in U-insertion/deletion editing in trypanosomes. Reduction in the levels of MRP1 (gBP21) and/or MRP2 (gBP25) mRNA by RNA interference in procyclic Trypanosoma brucei resulted in severe growth inhibition. It also resulted in the loss of both proteins, even when only one of the MRP mRNAs was reduced, indicating a mutual dependence for stability. Elimination of the MRPs gave rise to substantially reduced levels of edited CyB and RPS12 mRNAs but little or no reduction of the level of edited Cox2, Cox3, and A6 mRNAs as measured by poisoned primer extension analyses. In contrast, edited NADH-dehydrogenase (ND) subunit 7 mRNA was increased 5-fold in MRP1+2 double knock-down cells. Furthermore, MRP elimination resulted in reduced levels of Cox1, ND4, and ND5 mRNAs, which are never edited, whereas mitoribosomal 12 S rRNA levels were not affected. These data indicate that MRP1 and MRP2 are not essential for RNA editing per se but, rather, play a regulatory role in the editing of specific transcripts and other RNA processing activities.
References provided by Crossref.org
Lexis and Grammar of Mitochondrial RNA Processing in Trypanosomes
Combinatorial interplay of RNA-binding proteins tunes levels of mitochondrial mRNA in trypanosomes
TbUTP10, a protein involved in early stages of pre-18S rRNA processing in Trypanosoma brucei
A leucine aminopeptidase is involved in kinetoplast DNA segregation in Trypanosoma brucei
Trypanosome RNA editing: the complexity of getting U in and taking U out
The Fe/S cluster assembly protein Isd11 is essential for tRNA thiolation in Trypanosoma brucei
Flavodiiron protein from Trichomonas vaginalis hydrogenosomes: the terminal oxygen reductase