Dhar V, Searle B M, Athwal R S
Somat Cell Mol Genet. 1984 Nov;10(6):547-59. doi: 10.1007/BF01535220.
We have used a combination of chromosome-mediated gene transfer and microcell fusion techniques to transfer Chinese hamster chromosome 1 to mouse cells. Microcell hybrids containing a single hamster chromosome were analyzed to map genes on this chromosome. We have confirmed the assignment of seven markers (GSR, NP, EST-D, ADK, PEP-S, PGM2, and PEP-B) to hamster chromosome 1. Segregation among the linked markers was induced by X irradiation followed by selection for the retention or loss of human hprt. Cosegregation of markers in independent subclones made it possible to determine the gene order for the seven loci. The gene order proposed for these loci is as follows: pter-GSR-NP-EST-D-ADK-(PEP-S, PGM2)-PEP-B-qter. In addition GSR, NP, EST-D, and ADK have been assigned to pter-1q12; PEP-S and PGM2 to 1q12-1q21, and PEP-B to 1q32-1qter. These regional assignments and gene order on chromosome 1 have provided the information relevant to the linkages conserved between Chinese hamster, mouse, and man.
我们运用染色体介导的基因转移和微细胞融合技术相结合的方法,将中国仓鼠的1号染色体转移到小鼠细胞中。对含有单条仓鼠染色体的微细胞杂种进行分析,以定位该染色体上的基因。我们已证实七个标记物(谷胱甘肽还原酶(GSR)、磷酸核糖焦磷酸合成酶相关蛋白(NP)、酯酶D(EST-D)、腺苷激酶(ADK)、丝氨酸蛋白酶S(PEP-S)、磷酸葡萄糖变位酶2(PGM2)和丝氨酸蛋白酶B(PEP-B))定位于仓鼠1号染色体。通过X射线照射诱导连锁标记物之间的分离,随后选择保留或缺失人类次黄嘌呤磷酸核糖转移酶(hprt)。独立亚克隆中标记物的共分离使得确定这七个基因座的基因顺序成为可能。这些基因座的提议基因顺序如下:端粒-谷胱甘肽还原酶-磷酸核糖焦磷酸合成酶相关蛋白-酯酶D-腺苷激酶-(丝氨酸蛋白酶S、磷酸葡萄糖变位酶2)-丝氨酸蛋白酶B-着丝粒。此外,谷胱甘肽还原酶、磷酸核糖焦磷酸合成酶相关蛋白、酯酶D和腺苷激酶已被定位于端粒-1号染色体长臂1区1带2亚带(pter-1q12);丝氨酸蛋白酶S和磷酸葡萄糖变位酶2定位于1q12-1q21,丝氨酸蛋白酶B定位于1q32-1qter。1号染色体上的这些区域定位和基因顺序提供了与中国仓鼠、小鼠和人类之间保守连锁相关的信息。