Migeon B R, Miller C S
Science. 1968 Nov 29;162(3857):1005-6. doi: 10.1126/science.162.3857.1005.
Mouse somatic cells lacking thymidine kinase were mixed in culture with human diploid cells lacking hypoxanthine guanine phosphoribosyl transferase, and hybrid cells were isolated and maintained in a selective medium containing hypoxanthine, aminopterin, and thymidine. The hybrid cells at the time of isolation had karyotypes consisting predominantly of mouse chromosomes but with one human chromosome, a submetacentric member of group E, apparently giving thymidine kinase to the hybrid cell. However, after long-term propagation in the selective medium this chromosome has been lost, although cells continue to show thymidine kinase activity as demonstrated by the incorporation of (3)H-thy-midine into DNA in the hybrid cell. The hybrid cells have only mouse electro-phoretic variants for glucose-6-phosphate dehydrogenase, lactate dehydrogenase, and malate dehydrogenase, suggesting that the human genetic loci for these enzymes are not represented in the hybrid genome and may be unlinked to that for thymidine kinase.
将缺乏胸苷激酶的小鼠体细胞与缺乏次黄嘌呤鸟嘌呤磷酸核糖基转移酶的人二倍体细胞在培养中混合,分离出杂交细胞,并在含有次黄嘌呤、氨基蝶呤和胸苷的选择培养基中进行培养。分离时的杂交细胞的核型主要由小鼠染色体组成,但有一条人类染色体,即E组的亚中着丝粒染色体,显然它赋予了杂交细胞胸苷激酶活性。然而,在选择培养基中长期传代后,这条染色体已经丢失,尽管如通过将³H-胸苷掺入杂交细胞的DNA所证明的,细胞仍继续表现出胸苷激酶活性。杂交细胞仅具有小鼠葡萄糖-6-磷酸脱氢酶、乳酸脱氢酶和苹果酸脱氢酶的电泳变体,这表明这些酶的人类基因位点在杂交基因组中未表现出来,并且可能与胸苷激酶的基因位点不连锁。