SummaryRapid changes in mtDNA variants between generations have led to the bottleneck theory, which proposes a dramatic reduction in mtDNA numbers during early oo-genesis. We studied oocytes from a woman with hetero-plasmic expression of the mtDNA nt 8993 (TrG) mutation. Of seven oocytes analyzed, one showed no evidence of the mutation, and the remaining six had a mutant load ú95%. This skewed expression of the mutation in oocytes is not compatible with the conventional bottleneck theory. A possible explanation is that, during amplification of mtDNA in the developing oocyte, mtDNA from one mitochondrion is preferentially amplified. Thus, subsequent mature oocytes may contain predominantly wild-type or mutant mitochondrial genomes
Segregation of mutant mtDNA in human tissues and through the germline is debated, with no consensus...
Most humans carry a mixed population of mitochondrial DNA (mtDNA heteroplasmy) affecting ~1-2% of mo...
With a combined carrier frequency of 1:200, heteroplasmic mitochondrial DNA (mtDNA) mutations cause ...
SummaryRapid changes in mtDNA variants between generations have led to the bottleneck theory, which ...
SummaryWe have examined oocytes from a patient with Kearn-Sayre syndrome caused by mtDNA rearrangeme...
SummaryWe have examined oocytes from a patient with Kearn-Sayre syndrome caused by mtDNA rearrangeme...
PhD ThesisRegulation of mtDNA content is critical to normal human health and is often abnormal in mi...
We measured the proportion of mutant mtDNA (mutation load) in 82 primary oocytes from a woman who ha...
Segregation of mutant mtDNA in human tissues and through the germline is debated, with no consensus ...
Segregation of mutant mtDNA in human tissues and through the germline is debated, with no consensus ...
Segregation of mutant mtDNA in human tissues and through the germline is debated, with no consensus ...
Segregation of mutant mtDNA in human tissues and through the germline is debated, with no consensus...
Segregation of mutant mtDNA in human tissues and through the germline is debated, with no consensus ...
Segregation of mutant mtDNA in human tissues and through the germline is debated, with no consensus...
Segregation of mutant mtDNA in human tissues and through the germline is debated, with no consensus ...
Segregation of mutant mtDNA in human tissues and through the germline is debated, with no consensus...
Most humans carry a mixed population of mitochondrial DNA (mtDNA heteroplasmy) affecting ~1-2% of mo...
With a combined carrier frequency of 1:200, heteroplasmic mitochondrial DNA (mtDNA) mutations cause ...
SummaryRapid changes in mtDNA variants between generations have led to the bottleneck theory, which ...
SummaryWe have examined oocytes from a patient with Kearn-Sayre syndrome caused by mtDNA rearrangeme...
SummaryWe have examined oocytes from a patient with Kearn-Sayre syndrome caused by mtDNA rearrangeme...
PhD ThesisRegulation of mtDNA content is critical to normal human health and is often abnormal in mi...
We measured the proportion of mutant mtDNA (mutation load) in 82 primary oocytes from a woman who ha...
Segregation of mutant mtDNA in human tissues and through the germline is debated, with no consensus ...
Segregation of mutant mtDNA in human tissues and through the germline is debated, with no consensus ...
Segregation of mutant mtDNA in human tissues and through the germline is debated, with no consensus ...
Segregation of mutant mtDNA in human tissues and through the germline is debated, with no consensus...
Segregation of mutant mtDNA in human tissues and through the germline is debated, with no consensus ...
Segregation of mutant mtDNA in human tissues and through the germline is debated, with no consensus...
Segregation of mutant mtDNA in human tissues and through the germline is debated, with no consensus ...
Segregation of mutant mtDNA in human tissues and through the germline is debated, with no consensus...
Most humans carry a mixed population of mitochondrial DNA (mtDNA heteroplasmy) affecting ~1-2% of mo...
With a combined carrier frequency of 1:200, heteroplasmic mitochondrial DNA (mtDNA) mutations cause ...