Sánchez-Diz Paula, Gusmão Leonor, Beleza Sandra, Benítez-Páez Alfonso, Castro Azucena, García Oscar, Solla Lourdes Prieto, Geada Helena, Martín Pablo, Martínez-Jarreta Begoña, de Fátima Pinheiro Maria, Raimondi Eduardo, Silva de la Fuente Sandra María, Vide Maria Conceição, Whittle Martin R, Zarrabeitia María Teresa, Carracedo Angel, Amorim António
Institute of Legal Medicine, University of Santiago de Compostela, Compostela, Spain.
Forensic Sci Int. 2003 Aug 12;135(2):158-62. doi: 10.1016/s0379-0738(03)00200-7.
A collaborative exercise was carried out by the Spanish and Portuguese ISFG Working Group (GEP-ISFG) in order to evaluate the performance of two Y-chromosome STR PCR tetraplexes, which include the loci DYS461, GATA C4, DYS437 and DYS438 (GEPY I), and DYS460, GATA A10, GATA H4 and DYS439 (GEPY II). The participating laboratories were asked to type three samples for the eight markers, using a specific amplification protocol. In addition, two control samples, with known haplotypes, were provided. The results obtained by the 13 different participating laboratories were identical, except for two laboratories that failed to type correctly the same two samples for GATA C4. By sequence analyses, two different GATA C4 allele structures were found. One control sample (allele 21) and two questioned samples (allele 22, correctly typed by all the laboratories, and allele 25) presented the following repeat structure: (TCTA)4(TGTA)2(TCTA)2(TGTA)2(TCTA)n, but different from the one found for allele 26 in one sample included in this exercise, as well as in the second control sample (allele 23), namely (TCTA)4(TGTA)2(TCTA)2(TGTA)2(TCTA)2(TGTA)2(TCTA)n. The collaborative exercise results proved that both Y-tetraplexes produce good amplification results, with the advantage of being efficiently typed using different separation and detection methodologies. However, since GATA C4 repeat presents a complex structure, with alleles differing in sequence structure, efficient denaturing conditions should be followed in order to avoid typing errors due to sizing problems.
西班牙和葡萄牙国际法医遗传学会工作组(GEP - ISFG)开展了一项合作实验,以评估两种Y染色体STR PCR四重试剂盒的性能,这两种试剂盒分别包含基因座DYS461、GATA C4、DYS437和DYS438(GEPY I),以及DYS460、GATA A10、GATA H4和DYS439(GEPY II)。要求参与实验的实验室使用特定的扩增方案对三个样本进行这八个标记的分型。此外,还提供了两个已知单倍型的对照样本。除了两个实验室未能正确对相同的两个样本进行GATA C4分型外,13个不同参与实验室获得的结果是一致的。通过序列分析,发现了两种不同的GATA C4等位基因结构。一个对照样本(等位基因21)和两个受质疑样本(等位基因22,所有实验室均正确分型,以及等位基因25)呈现以下重复结构:(TCTA)4(TGTA)2(TCTA)2(TGTA)2(TCTA)n,但与本实验中包含的一个样本以及第二个对照样本(等位基因23)中的等位基因26的结构不同,等位基因26的结构为:(TCTA)4(TGTA)2(TCTA)2(TGTA)2(TCTA)2(TGTA)2(TCTA)n。合作实验结果证明,两种Y染色体四重试剂盒均能产生良好的扩增结果,优点是可使用不同的分离和检测方法进行高效分型。然而,由于GATA C4重复序列呈现复杂结构,等位基因在序列结构上存在差异,因此应遵循有效的变性条件,以避免因大小判断问题导致的分型错误。