期刊文献+

中国南方汉族人群STR位点遗传多态性研究及其在亲子鉴定中的应用 被引量:5

A genetic study on nine short tandem repeat(STR) loci among Han population in southern China and their application in parentage testing
下载PDF
导出
摘要 目的 调查中国南方汉族人群的 D8S1179、D2 1S11、D18S5 1、D5 S818、v WA、FGA、D3S135 8、D13S317、D7S82 0等 9个短串联重复 (STR)位点多态性 ,探索 STR基因分析在亲子鉴定案例中的应用价值。方法 应用 PCR复合扩增和四色荧光自动化检测技术对 5 74名南方汉族无关个体的 9个 STR位点作基因分型。结果 获得中国南方汉族人群中 9个 STR位点的等位基因频率 ,其基因型分布符合 Hardy- Weinberg平衡。经统计分析 ,D8S1179、D2 1S11、D18S5 1、D13S317、D7S82 0、D5 S818、v WA和 FGA位点属于高鉴别力、高杂合度、高信息含量的 STR位点 ,D3S135 8属于中高度多态性位点。 9个 STR位点的累积个体识别能力 (DP)、多态信息含量 (PIC)、杂合度 (H)和非父排除率 (PE)均为 0 .9999。在 2 10例亲子鉴定案例中 ,否定亲权的 2 8个案例中均至少有 3个位点不符 ;认定亲权的 182例中 ,亲子关系指数 (RCP)大于 99.73%的有 179例 (98.35 % ,179/ 182 ) ,另外 3例 (1.6 5 % ,3/ 182 ) RCP值为 95 .0 0 %~ 99.73%。结论 研究获得了中国南方汉族人群中 9个 STR位点的等位基因频率。应用这 9个 STR位点的等位基因鉴定 ,能成功地开展亲子鉴定 。 Objective To study the genetic polymorphism of nine STR loci which included D8S1179,D2 1S11,D18S5 1, D5 S818,D13S317,D7S82 0 ,D3S135 8,v WA,FGA among Han population in southern China and their application in parentage testing.Methods The nine STR loci of 5 74 unrelated individuals of Han population in the area of southern China were genotyped by PCR m ultiplex and autom ated analyzed.Results All allele frequencies were calculated and their distributions were in accordance with Hardy- Weinberg equilibrium.The results showed that eight STR loci had high inform ation except that D3S135 8was m iddle- high.The data of com bined discrimination power,polym orphism information content,heterozygosity and power of exclusion were all 0 .9999.Among the2 10 cases of parentage testing,2 8cases of exclusive paternity were incoordinate with more than 3loci.Among the 182 cases of determined paternal relation,the relative chance of paternity (RCP) in179cases(98.35 % ,179/ 182 ) was greater than99.73% .Conclusion We obtain all the allele frequencies of these nine STR loci am ong Han population in southern China.The results suggest that STR genetic study can be applied to parentage testing,and it will increase the RCP obviously.
出处 《临床输血与检验》 CAS 2003年第1期12-15,共4页 Journal of Clinical Transfusion and Laboratory Medicine
关键词 短串联重复序列 遗传多态性 基因分析 亲子鉴定 PCR复合扩增 四色荧光自动化检测技术 中国南方 汉族 Short tandem repeat locus Genetic polymorphism Parentage testing
  • 相关文献

参考文献5

二级参考文献23

  • 1[1]Walsh PS, Metzgar DA, Hignchi R, et al. Chelex- 100 as amedium for simple extraction of DNA for PCR- based typing fromforensic material. Bio Techniques, 1991, 10:506 ~ 513
  • 2Guo S W,Biometrics,1992年,48卷,361页
  • 3Nei M,Genetics,1978年,89卷,583页
  • 4Werrett DJ. The national DNAdatabase[J].J Forensic Sci Int, 1997, 88(4):33- 42.
  • 5Russ Hoyle. The FBI's national DNA database[J].Nature Biotechnology,1998,16:987.
  • 6Walsh PS, Metzger DA, Higuchi R.Chelex 100 as a medium for simple extraction ofDNA for PCR- based typing from forensic material[J]. Biotechniques,1991, 10:506-518.
  • 7Lazaruk P,Walsh P,Oaks F,et al.Genotyping of forensic short tandem repeat (STR)systems based on sizing precision in a capillary electrophoresis instrument[J].Electrophoresis,1998,19:86-93.
  • 8Fregeau CJ, Fourney RM. DNA typing with fluorescently tagged short tandem repeats:a sensitive and accurate approach to human identification[J].Biotechniques,1993,15:100- 119.
  • 9Perkin- Elmer Corporation.1998.AmpFl STRR Profiler Plus(tm) PCR amplificationkit[R]. User's Manual.
  • 10Perkin- Elmer Corporation.1998.AmpFl STRR CofilerTM PCR amplification kit[R].UserBulletin.

共引文献93

同被引文献42

引证文献5

二级引证文献12

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部