Recent studies have shown that in some cases,
fathers also pass on mitochondrial DNA. It began with studies of a 4-year-old boy who
presented with fatigue, muscle pain and
muscle weakness. Suspecting there might be some defects in the
child’s maternal mitochondria, researchers looked for abnormalities, which they
did not find. They did find that the child had mitochondria from both parents. Subsequently,
they also found biparental mitochondria in four other family members in several
generations. They found that at least four people across multiple generations
in the boy’s family have significant levels of biparental mitochondrial DNA. They
also found multiple members in two other families who also had biparental mitochondrial
DNA. According to the authors of the study published recently in PNAS, this discovery may help the development of new treatments for devastating mitochondrial disorders, which currently
can be treated but not “cured” per se. More tomorrow.
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