| Literature DB >> 26549459 |
Jitesh Neupane1, Sabitri Ghimire2, Mado Vandewoestyne3, Yuechao Lu2, Jan Gerris2, Rudy Van Coster4, Tom Deroo2, Dieter Deforce3, Stijn Vansteelandt5, Petra De Sutter2, Björn Heindryckx6.
Abstract
Variation in the level of mtDNA heteroplasmy in adult tissues is commonly seen in patients with a mixture of wild-type and mutant mtDNA. A mixture of different mtDNA variants may influence such variation and cause mtDNA segregation bias. We analyzed cellular heterogeneity in embryonic stem cells (ESCs) derived from a polymorphic mouse model containing NZB and BALB mtDNA genotypes. In ESCs, inter-colony heterogeneity varied up to 61%, whereas intra-colony heterogeneity varied up to 100%. Three out of five cell lines displayed nearly homoplasmic BALB and NZB mtDNA haplotypes in differentiated single cells. The proportion of NZB mtDNA genotype increased with progressive passaging (0.39%; p = 0.002). These results demonstrate the bimodal segregation of mtDNA haplotypes, indicating the occurrence of tissues with variable levels of heteroplasmies in individuals with mtDNA mutations. Furthermore, proliferation of one mtDNA genotype over another may pose the risk of accumulating mutant mtDNAs during subsequent cell divisions.Entities:
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Year: 2015 PMID: 26549459 DOI: 10.1016/j.celrep.2015.10.019
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423