Torroni A, Lott M T, Cabell M F, Chen Y S, Lavergne L, Wallace D C
Department of Genetics and Molecular Medicine, Emory University School of Medicine, Atlanta, GA 30322.
Am J Hum Genet. 1994 Oct;55(4):760-76.
mtDNA sequence variation was examined in 175 Caucasians from the United States and Canada by PCR amplification and high-resolution restriction-endonuclease analysis. The majority of the Caucasian mtDNAs were subsumed within four mtDNA lineages (haplogroups) defined by mutations that are rarely seen in Africans and Mongoloids. The sequence divergence of these haplogroups indicates that they arose early in Caucasian radiation and gave raise to modern European mtDNAs. Although ancient, none of these haplogroups is old enough to be compatible with a Neanderthal origin, suggesting that Homo sapiens sapiens displaced H. s. neanderthaliensis, rather than mixed with it. The mtDNAs of one of these haplogroups have a unique homoplasmic insertion between nucleotide pair (np) 573 and np 574, within the D-loop control region. This insertion makes these mtDNAs prone to a somatic mutation that duplicates a 270-bp portion of the D-loop region between np 309 and np 572. This finding suggests that certain nonpathogenic mtDNA mutations could predispose individuals to mtDNA rearrangements.
通过聚合酶链反应(PCR)扩增和高分辨率限制性内切酶分析,对来自美国和加拿大的175名高加索人的线粒体DNA(mtDNA)序列变异进行了检测。大多数高加索人的mtDNA被归入四个mtDNA谱系(单倍群),这些谱系由非洲人和蒙古人中罕见的突变所定义。这些单倍群的序列差异表明,它们在高加索人的辐射早期就已出现,并产生了现代欧洲人的mtDNA。尽管这些单倍群很古老,但没有一个古老到足以与尼安德特人的起源相契合,这表明智人取代了尼安德特人,而不是与之混合。其中一个单倍群的mtDNA在D环控制区域的核苷酸对(np)573和np 574之间有一个独特的纯质插入。这种插入使这些mtDNA易于发生体细胞突变,从而复制np 309和np 572之间D环区域的270个碱基对部分。这一发现表明,某些非致病性的mtDNA突变可能使个体易患mtDNA重排。