Womack J E, Davisson M T, Eicher E M, Kendall D A
Biochem Genet. 1977 Apr;15(3-4):347-55. doi: 10.1007/BF00484465.
A method for detecting two alleles at Np-1 (nucleoside phosphorylase) and three alleles at Es-10 (esterase 10) from mouse blood by cellulose acetate electrophoresis is described. The allelic constitution at these loci for 44 inbred strains and stocks was determined. The location of Np-1 on chromosome 14 was established by backcross experiments in which alleles at Np-1 and Robertsonian translocations were segregating. Es-10 was shown to be linked to Np-1, and the following genetic map of Chr 14 was constructed: centromere-(8.9 +/- 4.0 cM)-[Np-1, Wc]-(10.2 +/- 1.9 cM)-Es-10-(15.5 +/- 3.7 cM)-s. The homologous human loci, NP and ES-D, are not linked.
本文描述了一种通过醋酸纤维素电泳从小鼠血液中检测Np-1(核苷磷酸化酶)两个等位基因和Es-10(酯酶10)三个等位基因的方法。确定了44个近交系和品系在这些位点的等位基因组成。通过回交实验确定了Np-1在14号染色体上的位置,在该实验中Np-1等位基因和罗伯逊易位正在分离。结果表明Es-10与Np-1连锁,并构建了以下14号染色体的遗传图谱:着丝粒-(8.9±4.0厘摩)-[Np-1,Wc]-(10.2±1.9厘摩)-Es-10-(15.5±3.7厘摩)-s。同源的人类基因座NP和ES-D不连锁。