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首页> 外文期刊>Forensic science international >Twelve short tandem repeat loci Y chromosome haplotypes: Genetic analysis on populations residing in North America.
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Twelve short tandem repeat loci Y chromosome haplotypes: Genetic analysis on populations residing in North America.

机译:十二个短串联重复基因座Y染色体单倍型:居住在北美人口的遗传分析。

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A total of 2443 male individuals, previously typed for the 13 CODIS STR loci, distributed across the five North American population groups African American, Asian, Caucasian, Hispanic, and Native American were typed for the Y-STR loci DYS19, DYS385a/b, DYS389I/II, DYS390, DYS391, DYS392, DYS393, DYS437, DYS438 and DYS439 using the PowerPlex((R)) Y System. All population samples were highly polymorphic for the 12 Y-STR loci with the marker DYS385a/b being the most polymorphic across all sample populations. The Native American population groups demonstrated the lowest genetic diversity, most notably at the DYS393 and DYS437 loci. Almost all of the 12-locus haplotypes observed in the sample populations were represented only once in the database. Haplotype diversities were greater than 99.6% for the African Americans, Caucasians, Hispanics, and Asians. The Native Americans had the lowest haplotype diversities (Apaches, 97.0%; Navajo, 98.1%). Population substructure effects were greater for Y-haplotypes, compared with that for the autosomal loci. For the apportionment of variance for the 12 Y-STRs, the within sample population variation was the largest component (>98% for each major population group and approximately 97% in Native Americans), and the variance component contributed by the major population groups was less than the individual component, but much greater than among sample populations within a major group (11.79% versus 1.02% for African Americans/Caucasians/Hispanics and 15.35% versus 1.25% for all five major populations). When each major population is analyzed individually, the R(ST) values were low but showed significant among group heterogeneity. In 692 confirmed father-son pairs, 14 mutation events were observed with the average rate of 1.57x10(-3)/locus/generation (a 95% confidence bound of 0.83x10(-3) to 2.69x10(-3)). Since the Y-STR loci reside on the non-recombining region of the Y chromosome, the counting method is one approach suggested for conveying an estimate of the rarity of the Y-haplotype. Because the Y-STR loci are not all in disequilibrium to the same extent, the counting method is a very conservative approach. The data also support that autosomal STR frequencies can be multiplied by the upper bound frequency estimate of a Y-haplotype in the individual population group or those pooled into major population groups (i.e., Caucasian, African American, Hispanic, and Asian). These analyses support use of the haplotype population data for estimating Y-STR profile frequencies for populations residing in North America.
机译:总共有2443个男性个体,以前是为13个CODIS STR基因座分类的,分布在北美,非洲,白种人,西班牙裔和美洲原住民的五个北美人群中,它们的Y-STR基因座是DYS19,DYS385a / b,使用PowerPlex(R)Y系统的DYS389I / II,DYS390,DYS391,DYS392,DYS393,DYS437,DYS438和DYS439。对于12个Y-STR位点,所有种群样本都具有高度多态性,标记DYS385a / b在所有样本种群中都是多态性最高的。美国原住民群体显示出最低的遗传多样性,尤其是在DYS393和DYS437位点。在样本群体中观察到的几乎所有12个位点单倍型在数据库中仅代表一次。非裔美国人,高加索人,西班牙裔和亚洲人的单倍型多样性大于99.6%。美洲原住民的单倍型多样性最低(阿帕克斯(97.0%);纳瓦霍人(98.1%)。与常染色体基因座相比,Y-单倍型的种群亚结构效应更大。对于12个Y-STR的方差分配,样本内的人口变化是最大的组成部分(每个主要人群> 98%,在美洲原住民中约为97%),主要人群贡献的方差分量为低于单个组成部分,但比主要人群中的样本人群要大得多(非裔美国人/高加索人/西班牙裔美国人的比例为11.79%,而非裔美国人/白种人/西班牙人的比例为1.02%,而五个主要人群的比例分别为15.35%和1.25%)。当单独分析每个主要人群时,R(ST)值较低,但在群体异质性中显示出显着性。在692对确认的父子对中,观察到14个突变事件,平均发生率为1.57x10(-3)/基因座/世代(95%置信区间为0.83x10(-3)至2.69x10(-3))。由于Y-STR基因座位于Y染色体的非重组区域,因此计数方法是一种用于传达对Y单倍型稀有性的估计的方法。由于Y-STR位点并非全部处于不平衡状态,因此计数方法是一种非常保守的方法。数据还支持常染色体STR频率可以乘以单个人群或合并为主要人群(即高加索人,非裔美国人,西班牙裔和亚洲人)的Y型单体型的上限频率估计值。这些分析支持使用单倍型种群数据来估计居住在北美的种群的Y-STR分布频率。

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