Haines J L, Guillemette W, Rosen D, Brown R, Donaldson D, Patterson D
Molecular Neurogenetics Unit, Massachusetts General Hospital, Charlestown 02129.
Prog Clin Biol Res. 1993;384:51-61.
We have developed a genetic linkage map of chromosome 21 using 17 microsatellite marker polymorphisms. The markers span virtually the entire length of 21q, and define a sex-equal map of 56 cM. Extensive error checking has been used to provide an accurate map. All recombination events have been identified, allowing us to place within a small interval any new markers by genotyping only a few critical individuals. The resulting segregation data has been examined for several meiotic phenomena, including sex differences in recombination, age differences in recombination, interference, and segregation distortion.
我们利用17个微卫星标记多态性构建了21号染色体的遗传连锁图谱。这些标记几乎覆盖了21q的全长,并定义了一个56厘摩的性别均等图谱。我们采用了广泛的错误检查来提供准确的图谱。所有的重组事件都已被识别出来,这使我们仅通过对少数关键个体进行基因分型就能将任何新标记定位在一个小间隔内。我们已经对所得的分离数据进行了几种减数分裂现象的研究,包括重组中的性别差异、重组中的年龄差异、干涉和分离畸变。