Abstract
Mitochondrial DNA (mtDNA) sequence variants segregate in mutation and tissue-specific manners, but the mechanisms remain unknown. The segregation pattern of pathogenic mtDNA mutations is a major determinant of the onset and severity of disease. Using a heteroplasmic mouse model, we demonstrate that Gimap3, an outer mitochondrial membrane GTPase, is a critical regulator of this process in leukocytes. Gimap3 is important for T cell development and survival, suggesting that leukocyte survival may be a key factor in the genetic regulation of mtDNA sequence variants and in modulating human mitochondrial diseases.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Sequence
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Animals
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Base Sequence
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DNA, Mitochondrial / genetics*
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Embryo, Mammalian / cytology
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Female
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Fibroblasts / cytology
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Fibroblasts / metabolism
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GTP Phosphohydrolases / genetics
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GTP Phosphohydrolases / metabolism*
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GTP-Binding Proteins / genetics
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GTP-Binding Proteins / metabolism*
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Haplotypes / genetics*
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Hematopoietic System / metabolism
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Humans
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Kidney / metabolism
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Leukocytes / cytology
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Leukocytes / metabolism
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Liver / metabolism
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Male
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Membrane Proteins / genetics
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Membrane Proteins / metabolism*
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Mice
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Mice, Inbred BALB C
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Mice, Inbred C57BL
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Mice, Inbred Strains
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Mitochondrial Proteins / genetics
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Mitochondrial Proteins / metabolism*
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Molecular Sequence Data
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Sequence Homology, Amino Acid
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Sequence Homology, Nucleic Acid
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Spleen / metabolism
Substances
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DNA, Mitochondrial
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Ian4 protein, mouse
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Membrane Proteins
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Mitochondrial Proteins
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GTP Phosphohydrolases
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GTP-Binding Proteins