Lander E S, Botstein D
Science. 1987 Jun 19;236(4808):1567-70. doi: 10.1126/science.2884728.
An efficient strategy for mapping human genes that cause recessive traits has been devised that uses mapped restriction fragment length polymorphisms (RFLPs) and the DNA of affected children from consanguineous marriages. The method involves detection of the disease locus by virtue of the fact that the adjacent region will preferentially be homozygous by descent in such inbred children. A single affected child of a first-cousin marriage is shown to contain the same total information about linkage as a nuclear family with three affected children. Calculations show that it should be practical to map a recessive disease gene by studying DNA from fewer than a dozen unrelated, affected inbred children, given a complete RFLP linkage map. The method should make it possible to map many recessive diseases for which it is impractical or impossible to collect adequate numbers of families with multiple affected offspring.
一种用于绘制导致隐性性状的人类基因图谱的有效策略已经设计出来,该策略利用已绘制的限制性片段长度多态性(RFLP)以及近亲结婚所生患病子女的DNA。该方法通过这样一个事实来检测疾病位点:在这种近亲繁殖的子女中,相邻区域将优先通过遗传而成为纯合子。事实证明,表亲婚姻中一个患病子女所包含的关于连锁的总信息与一个有三个患病子女的核心家庭相同。计算表明,在有完整的RFLP连锁图谱的情况下,通过研究来自不到一打无关的、患病的近亲繁殖子女的DNA来绘制隐性疾病基因图谱应该是可行的。该方法应该能够绘制出许多隐性疾病的图谱,而对于这些疾病来说,收集足够数量的有多个患病后代的家庭是不切实际或不可能的。