Németi M, Bolodár A, Horváth K, Papp Z
Orv Hetil. 1989 Dec 3;130(49):2629-30, 2633.
The first step in the prenatal diagnosis of X-linked genetic disorders is the determination of the sex of the fetus. A new method for this purpose is based on recombinant DNA technology. The authors give a short account on their experiences with a Y specific DNA probe. Fetal DNA was prepared from chorionic villi taken at the 8th-12th weeks of gestation. The DNA was hybridised with the Y specific probe. This probe was isolated from the 3,4 kilobase human repeat sequence derived from heterochromatin of the Y chromosome and had 1000 times more affinity for male DNA than for female DNA. The method based on hybridisation with the Y specific probe should facilitate first-trimester prenatal sex determination of X-linked genetic disorders.
X连锁遗传病产前诊断的第一步是确定胎儿的性别。基于重组DNA技术的一种新方法可用于此目的。作者简要介绍了他们使用Y特异性DNA探针的经验。胎儿DNA取自妊娠第8至12周的绒毛膜绒毛。该DNA与Y特异性探针杂交。此探针从Y染色体异染色质衍生的3.4千碱基人类重复序列中分离出来,对男性DNA的亲和力比对女性DNA高1000倍。基于与Y特异性探针杂交的方法应有助于对X连锁遗传病进行孕早期产前性别鉴定。