Lacerenza D, Aneli S, Di Gaetano C, Critelli R, Piazza A, Matullo G, Culigioni C, Robledo R, Robino C, Calò C
Dipartimento di Scienze della Sanità Pubblica e Pediatriche, Università di Torino, Italy.
Dipartimento di Scienze Mediche, Università di Torino, Italy; HuGeF, Human Genetics Foundation, Torino, Italy.
Forensic Sci Int Genet. 2017 Mar;27:172-174. doi: 10.1016/j.fsigen.2016.12.009. Epub 2016 Dec 28.
Y-chromosomal variation of selected single nucleotide polymorphisms (SNPs) and 32 short tandem repeat (STR) loci was evaluated in Sardinia in three open population groups (Northern Sardinia, n=40; Central Sardinia, n=56; Southern Sardinia, n=91) and three isolates (Desulo, n=34; Benetutti, n=45, Carloforte, n=42). The tested Y-STRs consisted of Yfiler Plus markers and the seven rapidly mutating (RM) loci not included in the YFiler Plus kit (DYF399S1, DYF403S1ab, DYF404S1, DYS526ab, DYS547, DYS612, and DYS626). As expected, inclusion of additional Y-STR loci increased haplotype diversity (h), though complete differentiation of male lineages was impossible even by means of RM Y-STRs (h=0.99997). Analysis of molecular variance indicated that the three open populations were fairly homogeneous, whereas signs of genetic heterogeneity could be detected when the three isolates were also included in the analysis. Multidimensional scaling analysis showed that, even for extended haplotypes including RM Y-STR markers, Sardinians were clearly differentiated from populations of the Italian peninsula and Sicily. The only exception was represented by the Carloforte sample that, in accordance with its peculiar population history, clustered with Northern/Central Italian populations. The introduction of extended forensic Y-STR panels, including highly variable RM Y-STR markers, is expected to reduce the impact of population structure on haplotype frequency estimations. However, our results show that the availability of geographically detailed reference databases is still important for the assessment of the evidential value of a Y-haplotype match.
在撒丁岛的三个开放人群组(撒丁岛北部,n = 40;撒丁岛中部,n = 56;撒丁岛南部,n = 91)和三个隔离人群(德苏洛,n = 34;贝内图蒂,n = 45;卡尔洛福泰,n = 42)中,对选定的单核苷酸多态性(SNP)和32个短串联重复序列(STR)位点的Y染色体变异进行了评估。所测试的Y-STR由Yfiler Plus标记和YFiler Plus试剂盒中未包含的7个快速突变(RM)位点(DYF399S1、DYF403S1ab、DYF404S1、DYS526ab、DYS547、DYS612和DYS626)组成。正如预期的那样,纳入额外的Y-STR位点增加了单倍型多样性(h),尽管即使通过RM Y-STR也无法实现男性谱系的完全分化(h = 0.99997)。分子方差分析表明,三个开放人群相当同质,而当三个隔离人群也纳入分析时,可以检测到遗传异质性的迹象。多维标度分析表明,即使对于包括RM Y-STR标记的扩展单倍型,撒丁岛人与意大利半岛和西西里岛的人群也有明显差异。唯一的例外是卡尔洛福泰样本,根据其独特的群体历史,它与意大利北部/中部人群聚类。引入包括高度可变的RM Y-STR标记在内的扩展法医Y-STR面板,预计将减少群体结构对单倍型频率估计的影响。然而,我们的结果表明,地理详细的参考数据库的可用性对于评估Y单倍型匹配的证据价值仍然很重要。