| Literature DB >> 32786181 |
Melissa A Walker1, Caleb A Lareau1, Leif S Ludwig1, Amel Karaa1, Vijay G Sankaran1, Aviv Regev1, Vamsi K Mootha1.
Abstract
Many mitochondrial diseases are caused by mutations in mitochondrial DNA (mtDNA). Patients' cells contain a mixture of mutant and nonmutant mtDNA (a phenomenon called heteroplasmy). The proportion of mutant mtDNA varies across patients and among tissues within a patient. We simultaneously assayed single-cell heteroplasmy and cell state in thousands of blood cells obtained from three unrelated patients who had A3243G-associated mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes. We observed a broad range of heteroplasmy across all cell types but also found markedly reduced heteroplasmy in T cells, a finding consistent with purifying selection within this lineage. We observed this pattern in six additional patients who had heteroplasmic A3243G without strokelike episodes. (Funded by the Marriott Foundation and others.).Entities:
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Year: 2020 PMID: 32786181 PMCID: PMC7593775 DOI: 10.1056/NEJMoa2001265
Source DB: PubMed Journal: N Engl J Med ISSN: 0028-4793 Impact factor: 91.245