Document Detail


Nuclear DNA-encoded tRNAs targeted into mitochondria can rescue a mitochondrial DNA mutation associated with the MERRF syndrome in cultured human cells.
MedLine Citation:
PMID:  15317755     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Mitochondrial DNA (mtDNA) mutations are an important cause of human disease for which there is no efficient treatment. Our aim was to determine whether the A8344G mitochondrial tRNA(Lys) mutation, which can cause the MERRF (myoclonic epilepsy with ragged-red fibers) syndrome, could be complemented by targeting tRNAs into mitochondria from the cytosol. Import of small RNAs into mitochondria has been demonstrated in many organisms, including protozoans, plants, fungi and animals. Although human mitochondria do not import tRNAs in vivo, we previously demonstrated that some yeast tRNA derivatives can be imported into isolated human mitochondria. We show here that yeast tRNALys derivatives expressed in immortalized human cells and in primary human fibroblasts are partially imported into mitochondria. Imported tRNAs are correctly aminoacylated and are able to participate in mitochondrial translation. In transmitochondrial cybrid cells and in patient-derived fibroblasts bearing the MERRF mutation, import of tRNALys is accompanied by a partial rescue of mitochondrial functions affected by the mutation such as mitochondrial translation, activity of respiratory complexes, electrochemical potential across the mitochondrial membrane and respiration rate. Import of a tRNALys with a mutation in the anticodon preventing recognition of the lysine codons does not lead to any rescue, whereas downregulation of the transgenic tRNAs by small interfering RNA (siRNA) transiently abolishes the functional rescue, showing that this rescue is due to the import. These findings prove for the first time the functionality of imported tRNAs in human mitochondria in vivo and highlight the potential for exploiting the RNA import pathway to treat patients with mtDNA diseases.
Authors:
Olga A Kolesnikova; Nina S Entelis; Clarisse Jacquin-Becker; Francine Goltzene; Zofia M Chrzanowska-Lightowlers; Robert N Lightowlers; Robert P Martin; Ivan Tarassov
Related Documents :
16829155 - Leber's hereditary optic neuropathy: a multifactorial disease.
11854175 - Differentiation-specific effects of lhon mutations introduced into neuronal nt2 cells.
1719915 - Mitochondrial dna polymorphisms among hindus: a comparison with the tharus of nepal.
12013805 - Animal models for mitochondrial disease.
15881685 - The genetic basis of adaptation: lessons from concealing coloration in pocket mice.
21658325 - Adenosine a2a receptor polymorphisms in korean patients with systemic sclerosis.
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2004-08-18
Journal Detail:
Title:  Human molecular genetics     Volume:  13     ISSN:  0964-6906     ISO Abbreviation:  Hum. Mol. Genet.     Publication Date:  2004 Oct 
Date Detail:
Created Date:  2004-09-24     Completed Date:  2005-04-25     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  9208958     Medline TA:  Hum Mol Genet     Country:  England    
Other Details:
Languages:  eng     Pagination:  2519-34     Citation Subset:  IM    
Affiliation:
CNRS-FRE 2375, Institute of Physiology and Biological Chemistry, Université Louis Pasteur, 21 René Descartes, 67084 Strasbourg, France.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Anticodon / genetics
Cell Nucleus / genetics,  metabolism
Cells, Cultured
Cytoplasm / metabolism
DNA / genetics
DNA, Mitochondrial / genetics*
Electron Transport Complex IV / analysis
Fibroblasts / chemistry,  metabolism
Humans
MERRF Syndrome / genetics*,  metabolism
Mitochondria / chemistry,  metabolism*
Mutation / genetics*
Protein Biosynthesis
RNA Transport
RNA, Small Interfering / genetics
RNA, Transfer, Lys / analysis,  genetics*,  metabolism*
Saccharomyces cerevisiae / genetics
Chemical
Reg. No./Substance:
0/Anticodon; 0/DNA, Mitochondrial; 0/RNA, Small Interfering; 0/RNA, Transfer, Lys; 9007-49-2/DNA; EC 1.9.3.1/Electron Transport Complex IV

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Transgenic overexpression of human DMPK accumulates into hypertrophic cardiomyopathy, myotonic myopa...
Next Document:  Gene profiling links SCA1 pathophysiology to glutamate signaling in Purkinje cells of transgenic mic...