期刊文献+

用荧光标记MVR-PCR方法研究中国汉族人群DYF155S1基因座多态性 被引量:12

Studying the Polymorphism at DYF155S1 Locus in Chinese Han Population by MVR-PCR Marked with Fluorescence
下载PDF
导出
摘要 建立简便、实用的DYF15 5S1基因座基因分型的银染和荧光标记半自动分析方法 ,对中国汉族 15 5个无关男性个体血样本DNA进行分型 ,两种方法分型结果一致。 15 5人共检出 66种等位基因 ,有 3 8个等位基因仅出现 1次。根据图谱中第一条DNA片段及DNA条带数从小至大命名 ,频率最高的为 18和 2 2号等位基因 ,其第一条DNA片段大小为 180bp ,DNA条带数为连续的 16和 17个 ,频率均为 0 0 65。这一位点的基因多样性 (h)为 0 9789。 15 5人中有 2 5人表现为连续DNA谱带中有 1个或 2个DNA条带的丢失 (nullrepeat) ,序列分析证明丢失的DNA条带位置对应于 3型核心序列。结果表明 ,本文建立的分析方法能很好地揭示DYF15 5S1基因座 5′端多态性 ,是目前仅作1次PCR能获得个体Y染色体多态信息较高的技术。用本方法建立的中国汉族人群DYF15 5S1基因座等位基因频率资料 ,为群体遗传学研究及法医学应用提供了基础资料。 The simple and useful genotyping methods of DYF155S1 locus by silver staining and fluorescence detection have been established.The blood samples from 155 unrelated males in Chinese Han population were typed by these two methods respectively and the same results were obtained.Among the 155 samples 66 alleles were found,out of them 38 were observed once only.The most frequent alleles named 18 or 22,which frequency was 0 065,the size of their first DNA fragments was 180 bp and the number of fragments was 16 or 17.The gene diversity ( h ) was 0 9789.Out of the 155 samples,25 samples had one or two bands lost (null repeat) among the successive bands.It was demonstrated by sequencing that the position of the lost bands corresponded to type 3 repeats.Our results indicated that the method,which revealed the 5′ end diversity of DYF155S1 locus,was a technique that could obtain the most Y-specific polymorphic information only by one PCR reaction.The allele frequencies of DYF155S1 locus in Chinese Han population provided the basic data for the study of population genetics and forensic practices.
出处 《Acta Genetica Sinica》 SCIE CAS CSCD 北大核心 2003年第1期15-19,共5页
基金 广东省自然科学基金资助项目(编号 97-12 8) 中山医科大学"2 11工程"重点学科建设课题基金资助项目(编号 42 0 90 0 8)
关键词 荧光标记MVR-PCR方法 中国 汉族人群 DYF155S1基因座 MSY1 DNA多态性 MVR-PCR MSY1( DYF155S1 ) DNA polymorphism
  • 相关文献

参考文献13

二级参考文献12

  • 1金冬雁 黎孟枫(等).分子克隆实验指南(第二版)[M].北京:科学出版社,1992.60-69.
  • 2[1]Jobling MA,Bouzekri N,Taylor PG.Hypervariable digital DNA codes for human paternal lineages: MVR-PCR at the Ypecificminisatellite,MSY1 (DYF155S1) [J].Hum Mol Genet,2 1998,3 7:643
  • 3[2]Bouzekri N,Taylor PG,Hammer MF,et al.Novel mutation processes in the evolution of a haploid minisatellte,MSY1: array homogenization without homogernization [J].Hum Mol Genet,1998,7:655
  • 4[3]Hurles ME,Lrven C,Nicholson J,et al.European Ychromosomal lineages in poly-nesians: a contxast to the population structure revealed by mtDNA [J].Am J Hum Genet,1998,63:1793
  • 5[4]Jeffreys AJ,Tamaki K,Macleod A,et al.Ccmnplex gene conversion events in germ-line mutation at human minisatellites [J].Nat Genet,1994,6:136
  • 6[5]oda Y,Soejima M,Iiu YH,et al.Molecular basis for secretor type a (1,2) fucosyl-transferase gene deficiency in a Japanese population a fusion gene generated by unequalcrossover responsible for the enzyme deficiency [ J ].Am JHum Genet,61996,59:343
  • 7[6]Jeffreys AJ,Madeod A,Tamaki K,et al.Minisatellite repeat coxiing as a digital approach to DNA typing [J].Nature,1991,354(21):204
  • 8石国进.应急条件下的科学传播机制探究[J].中国科技论坛,2009(2):93-97. 被引量:18
  • 9何善亮.探究学习的存在价值及其实践限度[J].教育科学研究,2009(9):14-18. 被引量:12
  • 10张勇,张贵寅,孙艳阳,薛雅丽,杨焕杰,陈白滨,李璞.中国东北汉族及3个少数民族DYS19和DYS287多态性研究[J].人类学学报,1998,17(3):237-241. 被引量:8

共引文献51

同被引文献74

  • 1王保捷,丁梅,赵东,庞灏,李春梅.中国汉族与日本群体DYFl55S1基因座的遗传多态性[J].中国法医学杂志,2002,17(2):67-69. 被引量:3
  • 2周娟娟,洪素云.中国汉族人群15个STR基因座遗传多态性研究及法医学应用[J].中国免疫学杂志,2004,20(12):841-842. 被引量:10
  • 3侯一平,苟清,吴梅筠.人类短串联重复序列VWA基因座的群体遗传学研究[J].中华医学遗传学杂志,1996,13(2):65-69. 被引量:22
  • 4Nei M. Estimation of average heterozygosity and genetic distance from asmallnummber of individual [J]. Genetics,1978, 89:583-586.
  • 5Levedakou EN, Freeman DA, Budzynski M J, et al. Characterization and validation studies of PowerPlexTM 2. 1, a nine-locus short tandem repeat (STR) multiplex system and Penta D monoplex [ J ]. J Forensic Sci, 2002, 47 (4):757 - 772.
  • 6Krenke BE, Tereba A, Anderson SJ, et al. Validation of a 16 - locus fluorescent multiplex system [ J ]. J Forensic Sci,2002, 47 (4): 773-785.
  • 7Bacher J, Schumm JW. Development of highly polymorphic pentanucleotide tandem repeat loci with low stutter [ J ]. Profiles in DNA, 1998, 2 (2): 3 -6.
  • 8Walsh PS, Metzger DA, Higuchi R. Chelex 100 as a medium for simple extraction of DNA for PCR-based typing from forensic material [ J ]. Biotechniques, 1991, 10: 506 -513.
  • 9Bassam B J, Caetano-Anolles G, Gresshoff PM. Fast and sensitive silver staining of DNA in polyacrylamide gels [ J ].Anal Biochem, 1991, 196 (1): 80-83.
  • 10Guo SW, Thompson EA. Performing the exact test of HardyWeinberg proportion for multiple alleles [ J ]. Biometrics,1992, 48: 361 -372.

引证文献12

二级引证文献24

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