Denver D R, Morris K, Lynch M, Vassilieva L L, Thomas W K
Division of Molecular Biology and Biochemistry, School of Biological Sciences, University of Missouri-Kansas City, Kansas City, MO 64110, USA.
Science. 2000 Sep 29;289(5488):2342-4. doi: 10.1126/science.289.5488.2342.
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.
线粒体基因组中的突变与众多人类遗传疾病有关,并为系统发育、法医和群体遗传学研究提供重要数据。利用长期培养的秀丽隐杆线虫突变积累系,我们对线粒体基因组中的突变进行了大规模筛选,结果显示其突变率比之前的间接估计高出两个数量级,突变谱高度偏倚,有多个影响编码功能的突变,以及同聚核苷酸序列处的突变热点。