遗传学报
遺傳學報
유전학보
ACTA GENETICA SINICA
2006年
12期
1053-1059
,共7页
刘秋玲%吕德坚%祝家镇%陆惠玲%罗艳敏%方群
劉鞦玲%呂德堅%祝傢鎮%陸惠玲%囉豔敏%方群
류추령%려덕견%축가진%륙혜령%라염민%방군
X-STR%荧光复合扩增%毛细管电泳%多态性
X-STR%熒光複閤擴增%毛細管電泳%多態性
X-STR%형광복합확증%모세관전영%다태성
X-STR%fluorescent multiplex PCR%capillary electrophoresis%polymorphism
为研究DXS6803、DXS981和DXS6809 3个基因座多态性及其在法医学中的应用,建立X染色体基因座(DXS6803、DXS981和DXS6809)的荧光复合扩增体系.用荧光标记引物PCR技术复合扩增3个基因座,并用ABI PRISM 3100毛细管电泳及其软件进行基因分型.结果在中国汉族340名无关男性个体及195名无关女性个体中,DXS6803、DXS981和DXS6809三个基因座分别发现了13、12、11个等位基因,男性个体共检出183种单倍型,单倍型多样性为0.9926.结果表明这3个基因座有较高的多态性信息,在个体识别和亲权鉴定(特别是在缺失双亲的特殊检案)中有重要的应用价值.
為研究DXS6803、DXS981和DXS6809 3箇基因座多態性及其在法醫學中的應用,建立X染色體基因座(DXS6803、DXS981和DXS6809)的熒光複閤擴增體繫.用熒光標記引物PCR技術複閤擴增3箇基因座,併用ABI PRISM 3100毛細管電泳及其軟件進行基因分型.結果在中國漢族340名無關男性箇體及195名無關女性箇體中,DXS6803、DXS981和DXS6809三箇基因座分彆髮現瞭13、12、11箇等位基因,男性箇體共檢齣183種單倍型,單倍型多樣性為0.9926.結果錶明這3箇基因座有較高的多態性信息,在箇體識彆和親權鑒定(特彆是在缺失雙親的特殊檢案)中有重要的應用價值.
위연구DXS6803、DXS981화DXS6809 3개기인좌다태성급기재법의학중적응용,건립X염색체기인좌(DXS6803、DXS981화DXS6809)적형광복합확증체계.용형광표기인물PCR기술복합확증3개기인좌,병용ABI PRISM 3100모세관전영급기연건진행기인분형.결과재중국한족340명무관남성개체급195명무관녀성개체중,DXS6803、DXS981화DXS6809삼개기인좌분별발현료13、12、11개등위기인,남성개체공검출183충단배형,단배형다양성위0.9926.결과표명저3개기인좌유교고적다태성신식,재개체식별화친권감정(특별시재결실쌍친적특수검안)중유중요적응용개치.
This study was carried out to evaluate the value of three X-STR loci (DXS6803, DXS981and DXS6809) in forensic application and thereby investigate their polymorphism. The primer for each locus was labeled with fluorochrome 6-FAM. A fluorescent multiplex PCR for simultaneously amplifying three X-STR loci was set up. The PCR products that were obtained were analyzed using capillary electrophoresis and ABI PRISM 3100 Genetic Analyzer, with GENESCAN Analysis Software. When 340male and 195 female individuals of Han population in China were tested, 13, 12, and 11 alleles were observed for DXS6803,DXS981 and DXS6809, respectively. One hundred and eighty three haplotypes were detected in the male individuals. The haplotype diversity reached 0.9926. The results show that the three loci of the multiplex system provide significant information on polymorphism for forensic identification and paternity testing, particularly for complicated paternity deficient cases.