Budowle B, Wilson M R, DiZinno J A, Stauffer C, Fasano M A, Holland M M, Monson K L
Forensic Science Research and Training Center, FBI Academy, Quantico, VA 22135, USA.
Forensic Sci Int. 1999 Jul 12;103(1):23-35. doi: 10.1016/s0379-0738(99)00042-0.
Data from 1393 unrelated individuals have been compiled from eight population groups: African Americans, Africans (Sierra Leone), U.S. Caucasians, Austrians, French, Hispanics, Japanese, and Asian Americans. The majority of the mtDNA sequences were observed only once within each population group (i.e., ranging from a low of 60.3% (35/58) of the Asian American sequences to a high of 85.3% (93/109) of the French sequences). Genetic diversity ranged from 0.990 in the African sample to 0.998 in African Americans. Random match probability ranged from 2.50% in the Asian American sample to 0.52% in U.S. Caucasians. The average number of nucleotide differences between individuals in a database is greatest for the African American and African samples (14.1 and 13.1, respectively), and the least variable are the Caucasians (ranging from 7.2 to 8.4). Substitutions are the predominate polymorphism, and at least 92% of the substitutions are transitions. The most prevalent transversions are As substituted for Cs and Cs substituted for As. For most population groups these transversions occurred predominately in the HVI region; however, the African, African American, and Hispanic samples also demonstrated a large portion of their C to A and A to C transversions in the HVII region (at sites 186 and/or 189). Most insertions occur in the HVII region at sites 309.1 and 315.1, within a stretch of C's. Insertions of an additional C are common in all population groups. The sequence data were converted to SSO mtDNA types and compared with population data on Caucasians, Africans, Asians, Japanese, and Mexicans described by Stoneking et al. [M. Stoneking, D. Hedgecock, R.G. Higuchi, L. Vigilant, H.A. Erlich, Population variation of human mtDNA control region sequences detected by enzymatic amplification and sequence-specific oligonucleotide probes, Am. J. Hum. Genet. 48 (1991) 370-382] using an R x C contingency table test. Differences between major population groups (i.e., between African, Caucasian, and Asian) are quite evident, and similar ethnic population groups carried similar SSO polymorphism frequencies. There were only a few SSO types that showed significant differences between subpopulation groups. The SSO data alone can not be used to describe the population genetics with complete sequence data. However, the results of the SSO comparisons are similar to other analyses, and differences in sequence data in regions HVI and HVII are greater between major population groups than between subgroups.
已从八个种群组收集了1393名无血缘关系个体的数据:非裔美国人、非洲人(塞拉利昂)、美国白种人、奥地利人、法国人、西班牙裔、日本人及亚裔美国人。在每个种群组中,大多数线粒体DNA序列仅被观察到一次(即,从亚裔美国人序列的60.3%(35/58)的低比例到法国序列的85.3%(93/109)的高比例)。遗传多样性范围从非洲样本中的0.990到非裔美国人中的0.998。随机匹配概率范围从亚裔美国人样本中的2.50%到美国白种人中的0.52%。数据库中个体间核苷酸差异的平均数在非裔美国人和非洲样本中最大(分别为14.1和13.1),而白种人变异最小(范围从7.2到8.4)。替换是主要的多态性,并且至少92%的替换是转换。最常见的颠换是A替换C和C替换A。对于大多数种群组,这些颠换主要发生在高变区I;然而,非洲、非裔美国人和西班牙裔样本在高变区II(位点186和/或189)也显示出很大一部分C到A和A到C的颠换。大多数插入发生在高变区II的位点309.1和315.1,在一段C序列内。额外插入一个C在所有种群组中都很常见。序列数据被转换为序列特异性寡核苷酸(SSO)线粒体DNA类型,并使用R×C列联表检验与斯通金等人[M. 斯通金、D. 赫奇科克、R.G. 希古奇、L. 维吉兰特、H.A. 埃利希,通过酶促扩增和序列特异性寡核苷酸探针检测人类线粒体DNA控制区序列的种群变异,《美国人类遗传学杂志》48(1991)370 - 382]描述的白种人、非洲人、亚洲人、日本人及墨西哥人的种群数据进行比较。主要种群组之间(即非洲、白种人和亚洲之间)的差异非常明显,并且相似的种族种群组具有相似的SSO多态性频率。只有少数SSO类型在亚种群组之间显示出显著差异。仅SSO数据不能用于用完整序列数据描述种群遗传学。然而,SSO比较的结果与其他分析相似,并且高变区I和高变区II中序列数据在主要种群组之间的差异大于亚组之间的差异。