Myres Natalie M, Ekins Jayne E, Lin Alice A, Cavalli-Sforza L Luca, Woodward Scott R, Underhill Peter A
Sorenson Molecular Genealogy Foundation, Salt Lake City, Utah, USA.
Croat Med J. 2007 Aug;48(4):450-9.
To determine the human Y-chromosome haplogroup backgrounds of non-consensus DYS458.2 short tandem repeat alleles and evaluate their phylogenetic substructure and frequency in representative samples from the Middle East, Europe, and Pakistan.
Molecular characterization of lineages was achieved using a combination of Y-chromosome haplogroup defining binary polymorphisms and up to 37 short tandem repeat loci, including DYS388 to construct haplotypes. DNA sequencing of the DYS458 locus and median-joining network analyses were used to evaluate Y-chromosome lineages displaying the DYS458.2 motif.
We showed that the DYS458.2 allelic innovation arose independently on at least two distinctive binary haplogroup backgrounds and possibly a third as well. The partial allele length pattern was fixed in all haplogroup J1 chromosomes examined, including its known rare sub-haplogroups. Within the alternative R1b3 associated M405 defined sub-haplogroup, both DYS458.0 and DYS458.2 allele classes occurred. A single chromosome also allocated to the R1b3-M269*(xM405) classification. The physical position of the partial insertion/deletion occurrence within the normal tetramer tract differed distinctly in each haplogroup context.
While unusual DYS458.2 alleles are informative, additional information for other linked polymorphic loci is required when using such non-conforming alleles to infer haplogroup background and common ancestry.
确定非一致性DYS458.2短串联重复序列等位基因的人类Y染色体单倍群背景,并评估它们在中东、欧洲和巴基斯坦代表性样本中的系统发育亚结构和频率。
通过结合Y染色体单倍群定义的二元多态性和多达37个短串联重复序列位点(包括DYS388)来构建单倍型,从而实现谱系的分子特征分析。对DYS458位点进行DNA测序,并进行中位连接网络分析,以评估显示DYS458.2基序的Y染色体谱系。
我们发现,DYS458.2等位基因创新至少在两个不同的二元单倍群背景上独立出现,可能还有第三个背景。在所检测的所有单倍群J1染色体中,包括其已知的罕见亚单倍群,部分等位基因长度模式是固定的。在与R1b3相关的M405定义的替代亚单倍群中,同时出现了DYS458.0和DYS458.2等位基因类别。还有一条染色体被归为R1b3-M269*(xM405)分类。在每个单倍群背景下,正常四聚体区域内部分插入/缺失发生的物理位置明显不同。
虽然不寻常的DYS458.2等位基因具有信息价值,但在使用此类不一致的等位基因推断单倍群背景和共同祖先时,还需要其他连锁多态性位点的额外信息。