Hering S, Kuhlisch E, Szibor R
Institut für Rechtsmedizin der Medizinischen Fakultät, Technische Universität, Fetscherstrasse 74, 01307, Dresden, Germany.
Forensic Sci Int. 2001 Jun 1;119(1):42-6. doi: 10.1016/s0379-0738(00)00396-0.
This paper presents sequence and population genetic data of the X-linked DXS6789 short tandem repeat (STR). The tetranucleotide repeat polymorphism DXS6789, also known as CHLC.GATA31F01, is located at the Xq22.3 region. This locus is unlinked with DXS6807 and slightly linked with ARA, DXS9898 and HPRTB. In kinship testing, DXS6789 is suitable for concomitant use with DXS6807. Population genetic data were obtained by analysing 250 unrelated males and 315 females from East Germany. In this population, the STR exhibited 12 clearly distinguishable alleles ranging from 154 to 198bps in length. DXS6789 is characterised by the following data: polymorphic information content (PIC)=0.70; observed heterozygosity (Het)=0.78; mean exclusion chance (MEC)=0.70. A deviation from the Hardy-Weinberg equilibrium could not be detected. The investigations we performed in 243 mother-child and 161 father-child meioses did not reveal any mutations.
本文介绍了X连锁短串联重复序列(STR)DXS6789的序列和群体遗传数据。四核苷酸重复多态性DXS6789,也称为CHLC.GATA31F01,位于Xq22.3区域。该基因座与DXS6807不连锁,与ARA、DXS9898和HPRTB轻度连锁。在亲缘关系检测中,DXS6789适合与DXS6807联合使用。通过分析来自东德的250名无关男性和315名女性获得了群体遗传数据。在该群体中,STR表现出12个清晰可辨的等位基因,长度在154至198bps之间。DXS6789具有以下数据特征:多态信息含量(PIC)=0.70;观察杂合度(Het)=0.78;平均排除机会(MEC)=0.70。未检测到偏离哈迪-温伯格平衡的情况。我们在243对母子和161对父子减数分裂中进行的研究未发现任何突变。