Ferris S D, Sage R D, Prager E M, Ritte U, Wilson A C
Genetics. 1983 Nov;105(3):681-721. doi: 10.1093/genetics/105.3.681.
This study extends knowledge of mitochondrial DNA (mtDNA) diversity in mice to include 208 animals belonging to eight species in the subgenus Mus. Highly purified mtDNA from each has been subjected to high-resolution restriction mapping with respect to the known sequence of one mouse mtDNA. Variation attributed to base substitutions was encountered at about 200 of the 300 cleavage sites examined, and a length mutation was located in or near the displacement loop. The variability of different functional regions in this genome was as follows, from least to most: ribosomal RNA, transfer RNA, known proteins, displacement loop and unidentified reading frames. --Phylogenetic analysis confirmed the utility of the Sage and Marshall revision of mouse classification, according to which there are at least four species of commensal mice and three species of aboriginal mice in the complex that was formerly considered to be one species. The most thoroughly studied of these species is Mus domesticus, the house mouse of Western Europe and the Mediterranean region, which is the mitochondrial source of all 50 of the laboratory strains examined and of the representatives of wild house mice introduced by Europeans to North and South America during the past few hundred years. --The level of mtDNA variation among wild representatives of M. domesticus is similar to that for the Eastern European house mouse (M. musculus) and several other mammalian species. By contrast, among the many laboratory strains that are known or suspected to stem from the pet mouse trade, there is little interstrain variation, most strains having the "old inbred" type of domesticus mtDNA, whose frequency in the 145 wild mice examined is low, about 0.04. Also notable is the apparent homogeneity of mtDNA in domesticus races that have fixed six or more fused chromosomes and the close relationship of some of these mtDNAs to those of karyotypically normal mice. --In addition, this paper discusses fossil and other evidence for the view that in mice, as in many other mammals, the average rate of point mutational divergence in mtDNA is 2-4% per million years. From this, it is estimated that the commensal association between mice and our ancestors began more than a million years ago, i.e., at an early stage in the evolution of Homo erectus.
本研究将小鼠线粒体DNA(mtDNA)多样性的知识扩展到小家鼠亚属的8个物种的208只动物。已对每只动物高度纯化的mtDNA,相对于一种小鼠mtDNA的已知序列进行了高分辨率限制性图谱分析。在所检查的300个切割位点中,约200个位点出现了由碱基替换引起的变异,并且在置换环内或其附近发现了一个长度突变。该基因组中不同功能区域的变异性如下,从低到高:核糖体RNA、转运RNA、已知蛋白质、置换环和未鉴定的阅读框。——系统发育分析证实了萨奇和马歇尔对小鼠分类修订的实用性,根据该修订,在以前被认为是一个物种的复合体中,至少有4种共生小鼠和3种原生小鼠。这些物种中研究最深入的是小家鼠,即西欧和地中海地区的家鼠,它是所检查的所有50个实验室品系以及欧洲人在过去几百年中引入南北美洲的野生家鼠代表的线粒体来源。——小家鼠野生代表之间的mtDNA变异水平与东欧家鼠(小家鼠)和其他几种哺乳动物的相似。相比之下,在许多已知或疑似源自宠物鼠贸易的实验室品系中,品系间变异很小,大多数品系具有小家鼠mtDNA的“古老近交”类型,其在145只野生小鼠中的频率很低,约为0.04。同样值得注意的是,在已经固定了6条或更多融合染色体的小家鼠品种中,mtDNA具有明显的同质性,并且其中一些mtDNA与核型正常小鼠的mtDNA关系密切。——此外,本文还讨论了化石和其他证据,以支持这样一种观点,即在小鼠中,与许多其他哺乳动物一样,mtDNA中点突变分歧的平均速率为每百万年2 - 4%。据此估计,小鼠与我们祖先之间的共生关系始于一百多万年前,即在直立人进化的早期阶段。