Hashimi S, Miller O J
Cytogenet Cell Genet. 1976;17(1):35-41. doi: 10.1159/000130685.
A variant of the HPRT-A9 mouse cell line was fused with wild type diploid mouse bone marrow cells to obtain an HPRT+ line. The unique chromosomal features of the A9 parent, including the presence of a t(X;3) translocation and the absence of normal chromosomes 15,16, 17, 18, and the X, have permitted use of this intraspecific hybrid for chromosome mapping. Back-selection of hybrid cells in 8-azaguanine for loss of HPRT resulted in the loss of the Xchromosome derived from the diploid parent, providing evidence of the X-linkage of the HPRT locus.
将HPRT - A9小鼠细胞系的一个变体与野生型二倍体小鼠骨髓细胞融合,以获得一个HPRT + 细胞系。A9亲本独特的染色体特征,包括存在t(X;3)易位以及缺少正常的15、16、17、18号染色体和X染色体,使得这种种内杂种可用于染色体作图。在8 - 氮杂鸟嘌呤中对杂种细胞进行反向选择以去除HPRT,导致来自二倍体亲本的X染色体丢失,这为HPRT基因座的X连锁提供了证据。