Lukey T, Neote K, Loman J F, Unger A E, Biddle F G, Snyder F F
Biochem Genet. 1985 Apr;23(3-4):347-56. doi: 10.1007/BF00504331.
An improved method for detecting four Np-1 (purine nucleoside phosphorylase) alleles in mouse erythrocytes by cellulose acetate electrophoresis is described. The previous linkage of Np-1 and Es-10 (esterase-10) was confirmed, with a map distance of 13.0 +/- 2.6 cM. Np-2 was detected by either specific activity assay or starch gel electrophoresis and shown to be linked to Es-10, 15.9 +/- 3.1 cM, on chromosome 14. No recombinants between Np-1 and Np-2 were observed in 52 offspring, indicating either that these loci are either closely associated or that Np-2 represents simply a property of existing allelic products of the Np-1 locus.
本文描述了一种通过醋酸纤维素电泳检测小鼠红细胞中四种Np-1(嘌呤核苷磷酸化酶)等位基因的改进方法。先前确定的Np-1和Es-10(酯酶-10)的连锁关系得到证实,图距为13.0±2.6厘摩。通过比活性测定或淀粉凝胶电泳检测到Np-2,并表明其与14号染色体上的Es-10连锁,图距为15.9±3.1厘摩。在52个后代中未观察到Np-1和Np-2之间的重组体,这表明这些基因座要么紧密相关,要么Np-2仅仅代表Np-1基因座现有等位基因产物的一种特性。