| Literature DB >> 11009418 |
D R Denver1, K Morris, M Lynch, L L Vassilieva, W K Thomas.
Abstract
Mutations in the mitochondrial genome have been implicated in numerous human genetic disorders and offer important data for phylogenetic, forensic, and population genetic studies. Using a long-term series of Caenorhabditis elegans mutation accumulation lines, we performed a wide-scale screen for mutations in the mitochondrial genome that revealed a mutation rate that is two orders of magnitude higher than previous indirect estimates, a highly biased mutational spectrum, multiple mutations affecting coding function, as well as mutational hotspots at homopolymeric nucleotide stretches.Entities:
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Year: 2000 PMID: 11009418 DOI: 10.1126/science.289.5488.2342
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728