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两个Y染色体短串联重复序列基因座的遗传多态性 被引量:2

Polymorphic analysis of two Y chromosome short tandem repeat loci in Chinese Chengdu Han population
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摘要 目的调查DYS508、DYS516两个Y染色体短串联重复序列基因座的遗传多态性在成都汉族群体中的分布。方法用PCR扩增、非变性聚丙烯酰胺凝胶电泳分型;构建等位基因分型标准物;对所有等位基因测序,按照国际法医遗传学会原则命名等位基因。结果获得DYS508、DYS516基因座等位基因个数分别为6、6;基因变异度分别为0.7242、0.7931;单倍型变异度、个人识别能力和非父排除率均为0·9397。结论DYS508、DYS516这两个Y染色体短串联重复序列均具有较好的遗传多态性,可用于法医学的混合斑分析和父系亲属间的亲权关系鉴定。 Objective To reveal the distribution of genetic polymorphism of two novel Y chromosome short tandem repeat (Y-STR) loci (DYS508, DYS516) in Chinese Chengdu Han population. Methods Two Y-STR loci were amplified with PCR. The products of PCR were analyzed with polyacrylamide gel electrophoresis. Each allele of these 2 Y-STR loci was sequenced and the allele ladders were constructed. Alleles of these Y-STR loci were nominated according to recommendations of the International Society of Forensic Genetics (ISFG). Results Six and 6 alleles were observed in loci DYS508 and DYS516 respectively. The gene diversity of DYS508 and DYS516 was 0.7242 and 0.7931 respectively. The diversity of haplotype for these Y-STR loci was 0.9397. The value of discrimination power and the exclusion chance of paternity for these Y-STR loci were same as the value of haplotype diversity. Conclusion Both Y-STR loci are high genetic polymorphic. They are benificial to the test of male-female mixtures and paternity identification in forensic science.
出处 《中华医学遗传学杂志》 CAS CSCD 北大核心 2006年第6期683-684,共2页 Chinese Journal of Medical Genetics
关键词 Y染色体 短串联重复序列 单倍型 遗传多态性 Y-chromosome short tandem repeat haplotype genetic polymorphism
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参考文献10

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共引文献39

同被引文献11

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  • 7Hou YP,Zhang J,Li YB,et al.Allele sequences of six new Y -STR loci and haplotypes in the Chinese Han population[J].Forensic Science International,2001,118:147-152.
  • 8郝旭宇,吴晓兵,牛恺,张更谦,郭大玮,牛四平,高云海.新Y染色体DYS651在山西汉族人群中遗传多态性调查[J].湖北民族学院学报(医学版),2008,25(1):1-3. 被引量:1
  • 9赵亚娣,梁景青,郭大玮,张更谦,贠克明,徐晓莉.山西汉族人群DYS715和DYS717基因座遗传多态性[J].中国法医学杂志,2008,23(5):338-339. 被引量:1
  • 10侯一平,吴谨,李英碧,张霁,张思仲,褚嘉佑.Y染色体特异短串联重复序列初步研究[J].中华医学遗传学杂志,1999,16(2):65-69. 被引量:40

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