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从单个卵裂球中扩增β-珠蛋白基因。

Amplification of beta-globin gene from single blastomeres.

作者信息

Wu R C, Kuo P L

机构信息

Department of Obstetrics and Gynecology, National Cheng Kung University Medical Center, Tainan, Taiwan, R.O.C.

出版信息

J Formos Med Assoc. 1994 Mar;93(3):200-4.

PMID:7920058
Abstract

Prenatal diagnosis of beta-thalassemia can be performed by chorionic villus sampling as early as the ninth gestational week, and early amniocentesis within 12 weeks of gestation. Selective abortion or termination should be suggested if the fetus is affected. With polymerase chain reaction (PCR) and micromanipulation techniques, the preimplantation diagnosis of beta-thalassemia has become possible. A total of 60 single blastomeres were collected and equally divided at random into two groups. Eight DNA primers (A to H) were designed for 15 mutations of beta-thalassemia in Chinese people. Two beta-globin gene fragments (602 bp and 423 bp) were amplified by PCR through two sequential reactions with two sets of primers (A+B and C+D, E+F and G+H), respectively. The amplified products were confirmed by Southern blotting with DNA probes hybridization. The amplification rates were 54% (16/30) and 60% (18/30), respectively. All of the positive and negative controls showed the presence or absence of amplification, respectively. Our study provides a possible approach for the preimplantation diagnosis of beta-thalassemia.

摘要

早在妊娠第9周时,可通过绒毛取样进行β地中海贫血的产前诊断,在妊娠12周内可进行早期羊膜腔穿刺术。如果胎儿受到影响,应建议选择性流产或终止妊娠。随着聚合酶链反应(PCR)和显微操作技术的发展,β地中海贫血的植入前诊断已成为可能。总共收集了60个单个卵裂球,并随机均分为两组。针对中国人β地中海贫血的15种突变设计了8种DNA引物(A至H)。通过分别用两组引物(A+B和C+D、E+F和G+H)进行两个连续反应,通过PCR扩增两个β珠蛋白基因片段(602 bp和423 bp)。扩增产物通过DNA探针杂交的Southern印迹法进行确认。扩增率分别为54%(16/30)和60%(18/30)。所有阳性和阴性对照分别显示出扩增的存在或不存在。我们的研究为β地中海贫血的植入前诊断提供了一种可能的方法。

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