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Recurrent Tissue-Specific mtDNA Mutations Are Common in Humans
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نویسنده
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samuels d.c. ,li c. ,li b. ,song z. ,torstenson e. ,boyd clay h. ,rokas a. ,thornton-wells t.a. ,moore j.h. ,hughes t.m. ,hoffman r.d. ,haines j.l. ,murdock d.g. ,mortlock d.p. ,williams s.m.
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منبع
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plos genetics - 2013 - دوره : 9 - شماره : 11
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چکیده
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Mitochondrial dna (mtdna) variation can affect phenotypic variation; therefore,knowing its distribution within and among individuals is of importance to understanding many human diseases. intra-individual mtdna variation (heteroplasmy) has been generally assumed to be random. we used massively parallel sequencing to assess heteroplasmy across ten tissues and demonstrate that in unrelated individuals there are tissue-specific,recurrent mutations. certain tissues,notably kidney,liver and skeletal muscle,displayed the identical recurrent mutations that were undetectable in other tissues in the same individuals. using rflp analyses we validated one of the tissue-specific mutations in the two sequenced individuals and replicated the patterns in two additional individuals. these recurrent mutations all occur within or in very close proximity to sites that regulate mtdna replication,strongly implying that these variations alter the replication dynamics of the mutated mtdna genome. these recurrent variants are all independent of each other and do not occur in the mtdna coding regions. the most parsimonious explanation of the data is that these frequently repeated mutations experience tissue-specific positive selection,probably through replication advantage. © 2013 samuels et al.
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آدرس
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center for human genetics research,department of molecular physiology and biophysics,vanderbilt university school of medicine,nashville,tn, United States, center for human genetics research,department of biostatistics,vanderbilt university school of medicine,nashville,tn, United States, center for human genetics research,department of molecular physiology and biophysics,vanderbilt university school of medicine,nashville,tn, United States, center for human genetics research,vanderbilt university school of medicine,nashville,tn, United States, center for human genetics research,vanderbilt university school of medicine,nashville,tn, United States, center for human genetics research,department of molecular physiology and biophysics,vanderbilt university school of medicine,nashville,tn, United States, department of biological sciences,vanderbilt university school of medicine,nashville,tn, United States, center for human genetics research,department of molecular physiology and biophysics,vanderbilt university school of medicine,nashville,tn, United States, dartmouth medical school,department of genetics,computational genetics lab,lebanon,nh, United States, center for human genetics research,vanderbilt university school of medicine,nashville,tn, United States, department of pathology,vanderbilt university school of medicine,nashville,tn, United States, center for human genetics research,department of molecular physiology and biophysics,vanderbilt university school of medicine,nashville,tn, United States, center for human genetics research,department of molecular physiology and biophysics,vanderbilt university school of medicine,nashville,tn, United States, center for human genetics research,department of molecular physiology and biophysics,vanderbilt university school of medicine,nashville,tn, United States, center for human genetics research,department of molecular physiology and biophysics,vanderbilt university school of medicine,nashville,tn,united states,dartmouth medical school,department of genetics,computational genetics lab,lebanon,nh, United States
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Authors
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