caa a22 4500 397575734 CHVBK 20180308164855.0 cr unu---uuuuu 161202e199602 xx s 000 0 eng 10.1093/hmg/5.2.197 doi (NATIONALLICENCE)oxford-10.1093/hmg/5.2.197 Relationship of Genotype to Phenotype in Fibroblast-derived Transmitochondrial Cell Lines Carrying the 3243 Mutation Associated with the Melas Encephalomyopathy: Shift towards Mutant Genotype and Role of mtDNA Copy Number [Elektronische Daten] [Herman A. C. M. Bentlage, Giuseppe Attardi] Transmitochondrial cell lines were isolated by fusing mtDNA-less ρ°206 cells with enucleated fibroblasts derived from four members of a pedigree carrying in their muscle varying proportions of the mutation at position 3243 in the tRNALeu(UUR) gene associated with the MELAS encephalomyopathy. The mitochondrial transformants derived from an asymptomatic individual were all homoplasmic for wild-type mtDNA. The proportion of wild-type transformants derived from clinically affected members of the pedigree appeared to decrease in correspondence with an increase in severity of the clinical symptoms of the cell donor. Furthermore, the average proportion of wild-type mtDNA in the transformants derived from each member of the pedigree was very similar to that found in mtDNA from the fibroblasts of that individual, suggesting that the distribution of genotypes in the transformants reflected fairly closely that in the fibroblasts. The genotype and phenotype of ten transformants derived from one severely affected individual were investigated during continuous culture up to 17-24 weeks after the transformation step. Six heteroplasmic clones showed a progressive increase in the proportion of mutant mtDNA, whereas the mitochondrial genotype remained constant in four clones apparently homoplasmic for wild-type mtDNA or nearly homoplasmic for mutant mtDNA. An analysis of the rate of repopulation of ρ°206 cells with fibroblast-derived mtDNA revealed a large variability among different transformants, with the full re-establishment of the control ratio of mtDNA to nuclear DNA being observed between ∼6 weeks and more than 22 weeks after the transformation step. An increase in rate of O2 consumption generally accompanied the increase in mtDNA copy number of the transformants, pointing to the important role of the mtDNA copy number in determining the phenotype of a cell. The observation that a very small amount of wild-type mtDNA (2 to 5% of the control level), coexisting with strongly predominant mutant mtDNA, conferred upon the transformants a substantial respiratory capacity (50% or more) and the evidence of proportionality between O2 consumption rate and mtDNA copy number, which occurred at widely different mutant to wild-type mtDNA ratios, strongly suggest a contribution of the mutant mtDNA to the cell respiratory competence. © 1996 Oxford University Press Bentlage Herman A. C. M. Division of Biology, California Institute of Technology, Pasadena, CA 91125, USA aut Attardi Giuseppe Division of Biology, California Institute of Technology, Pasadena, CA 91125, USA aut Human Molecular Genetics Oxford University Press 5/2(1996-02), 197-205 0964-6906 5:2<197 1996 5 hmg https://doi.org/10.1093/hmg/5.2.197 text/html Onlinezugriff via DOI 1 research-article jats NATIONALLICENCE 856 40 https://doi.org/10.1093/hmg/5.2.197 text/html Onlinezugriff via DOI NATIONALLICENCE 700 1- Bentlage Herman A. C. M. Division of Biology, California Institute of Technology, Pasadena, CA 91125, USA aut NATIONALLICENCE 700 1- Attardi Giuseppe Division of Biology, California Institute of Technology, Pasadena, CA 91125, USA aut NATIONALLICENCE 773 0- Human Molecular Genetics Oxford University Press 5/2(1996-02), 197-205 0964-6906 5:2<197 1996 5 hmg Metadata rights reserved CC BY-NC-4.0 http://creativecommons.org/licenses/by-nc/4.0 nationallicence BK010053 XK010053 XK010000 NATIONALLICENCE NATIONALLICENCE NL-oxford