Monnat R J, Loeb L A
Proc Natl Acad Sci U S A. 1985 May;82(9):2895-9. doi: 10.1073/pnas.82.9.2895.
Recombinant DNA techniques have been used to quantitate the amount of nucleotide sequence divergence in the mitochondrial DNA population of individual normal humans. Mitochondrial DNA was isolated from the peripheral blood lymphocytes of five normal humans and cloned in M13 mp11; 49 kilobases of nucleotide sequence information was obtained from 248 independently isolated clones from the five normal donors. Both between- and within-individual differences were identified. Between-individual differences were identified in approximately 1/200 nucleotides. In contrast, only one within-individual difference was identified in 49 kilobases of nucleotide sequence information. This high degree of mitochondrial nucleotide sequence homogeneity in human somatic cells is in marked contrast to the rapid evolutionary divergence of human mitochondrial DNA and suggests the existence of mechanisms for the concerted preservation of mammalian mitochondrial DNA sequences in single organisms.
重组DNA技术已被用于定量个体正常人类线粒体DNA群体中的核苷酸序列差异量。从五个正常人类的外周血淋巴细胞中分离出线粒体DNA,并克隆到M13 mp11中;从五个正常供体的248个独立分离的克隆中获得了49千碱基的核苷酸序列信息。个体间和个体内的差异均被识别出来。个体间差异在大约1/200个核苷酸中被识别出来。相比之下,在49千碱基的核苷酸序列信息中仅识别出一个个体内差异。人类体细胞中线粒体核苷酸序列的这种高度同质性与人类线粒体DNA的快速进化分歧形成了鲜明对比,并表明在单个生物体中存在协调保存哺乳动物线粒体DNA序列的机制。