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
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem, Research Support, U.S. Gov't, P.H.S.
Grantová podpora
AI14102
NIAID NIH HHS - United States
PubMed
15504736
DOI
10.1074/jbc.m405933200
PII: S0021-9258(20)76285-X
Knihovny.cz E-zdroje
- MeSH
- časové faktory MeSH
- DNA primery chemie MeSH
- editace RNA MeSH
- glycerol chemie MeSH
- imunoprecipitace MeSH
- klonování DNA MeSH
- messenger RNA metabolismus MeSH
- mitochondriální proteiny metabolismus fyziologie MeSH
- northern blotting MeSH
- plazmidy metabolismus MeSH
- proteiny vázající RNA metabolismus fyziologie MeSH
- protozoální proteiny metabolismus fyziologie MeSH
- RNA interference * MeSH
- RNA protozoální MeSH
- RNA ribozomální metabolismus MeSH
- RNA chemie metabolismus MeSH
- Southernův blotting MeSH
- transfekce MeSH
- Trypanosoma brucei brucei metabolismus MeSH
- vazba proteinů MeSH
- western blotting MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, U.S. Gov't, P.H.S. MeSH
- Názvy látek
- DNA primery MeSH
- gBP21 protein, Trypanosoma brucei MeSH Prohlížeč
- gBP25 protein, Trypanosoma brucei MeSH Prohlížeč
- glycerol MeSH
- messenger RNA MeSH
- mitochondriální proteiny MeSH
- proteiny vázající RNA MeSH
- protozoální proteiny MeSH
- RNA protozoální MeSH
- RNA ribozomální MeSH
- RNA, ribosomal, 12S MeSH Prohlížeč
- 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.
Citace poskytuje Crossref.org
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