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泰国人群与西欧人群中与凝血因子VIII和凝血因子IX基因相关的十种DNA多态性的等位基因频率比较。

A comparison of the allelic frequencies of ten DNA polymorphisms associated with factor VIII and factor IX genes in Thai and Western European populations.

作者信息

Goodeve A C, Chuansumrit A, Sasanakul W, Isarangkura P, Preston F E, Peake I R

机构信息

Department of Medicine and Pharmacology, Royal Hallamshire Hospital, Sheffield.

出版信息

Blood Coagul Fibrinolysis. 1994 Feb;5(1):29-35. doi: 10.1097/00001721-199402000-00005.

Abstract

The frequency of five factor VIII gene intragenic and linked DNA polymorphisms and five factor IX gene intragenic polymorphisms was studied in Thai females. The polymorphisms in the FVIII gene were detected by restriction enzymes BclI, XbaI, BglI and at linked loci DX13 (DXS15) and St14 (DXS52) by BglII and TaqI, respectively, and in the FIX gene by MseI, DdeI, XmnI, TaqI and HhaI. With the exception of the BglI restriction fragment length polymorphism (RFLP), which is absent in Thais, factor VIII polymorphism frequencies were similar in Thais and Caucasians. Combined use of XbaI and TaqI/St14 resulted in a heterozygosity rate of greater than 90% in Thai females. For FIX, the recently described MseI RFLP in the 5' flanking region was the most informative polymorphism in Thais, 43% of females being heterozygous. The other four polymorphisms added little to the overall heterozygosity rate. The appropriate polymorphisms were used to track defective factor VIII and IX genes through 22 Thai pedigrees with haemophilia to enable carrier status to be assigned to female family members. The information obtained during this study will form the basis for carrier detection and prenatal diagnosis of haemophilia A and B by DNA polymorphism analysis in Thailand.

摘要

对泰国女性的5种凝血因子VIII基因内部及连锁DNA多态性和5种凝血因子IX基因内部多态性的频率进行了研究。分别用限制性内切酶BclI、XbaI、BglI检测FVIII基因多态性,用BglII和TaqI分别检测连锁位点DX13(DXS15)和St14(DXS52),用MseI、DdeI、XmnI、TaqI和HhaI检测FIX基因多态性。除了泰国人不存在的BglI限制性片段长度多态性(RFLP)外,泰国人和高加索人的凝血因子VIII多态性频率相似。联合使用XbaI和TaqI/St14,泰国女性的杂合率大于90%。对于FIX,最近在5'侧翼区域描述的MseI RFLP是泰国人中信息量最大的多态性,43%的女性为杂合子。其他四种多态性对总体杂合率的贡献不大。利用合适的多态性通过22个患有血友病的泰国家系追踪有缺陷的凝血因子VIII和IX基因,以便为女性家庭成员确定携带者状态。本研究期间获得的信息将为泰国通过DNA多态性分析进行血友病A和B携带者检测及产前诊断奠定基础。

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