Law M L, Kao F T
Cytogenet Cell Genet. 1979;24(2):102-14. doi: 10.1159/000131363.
Karyological analysis was performed on a series of human-Chinese hamster cell hybrids containing deletions of human chromosome 12. Chromosome breakage was produced by treatment of the cells with either X-rays or 5-bromodeoxyuridine and near-visible light. The hybrid clones were analyzed for the presence or absence of the following five human gene markers known to be located on chromosome 12: triosephosphate isomerase-1 (TPI1), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), lactate dehydrogenase-B (LDHB), serine hydroxymethyltransferase (SHMT), and peptidase-B (PEPB). Based on the correlation between the isozyme markers and karyological analysis of these clones, a regional map of the five human genes on chromosome 12 was established. The linear order for these genes is: pter-TPI1-GAPDH-LDHB-centromere-SHMT-PEPB-qter. The locations of these genes are: TPI1, GAPDH, LDHB: pter leads to p12; SHMT: q12 leads to q14; PEPB: q14 leads to qter. Statistical analysis similar to that of Goss and Harris (1975, 1977a, b) has been performed on the segregation data in the hybrid clones. The statistical map, in general, agrees with the cytogenetic map and further localizes PEPB to 12q21.
对一系列含有人类12号染色体缺失的人-中国仓鼠细胞杂种进行了核型分析。通过用X射线或5-溴脱氧尿苷和近可见光处理细胞来产生染色体断裂。分析杂种克隆中是否存在已知位于12号染色体上的以下五种人类基因标记:磷酸丙糖异构酶-1(TPI1)、甘油醛-3-磷酸脱氢酶(GAPDH)、乳酸脱氢酶-B(LDHB)、丝氨酸羟甲基转移酶(SHMT)和肽酶-B(PEPB)。基于这些克隆的同工酶标记与核型分析之间的相关性,建立了12号染色体上这五个人类基因的区域图谱。这些基因的线性顺序是:端粒-TPI1-GAPDH-LDHB-着丝粒-SHMT-PEPB-端粒。这些基因的位置是:TPI1、GAPDH、LDHB:端粒到p12;SHMT:q12到q14;PEPB:q14到端粒。已对杂种克隆中的分离数据进行了与戈斯和哈里斯(1975年、1977年a、b)类似的统计分析。统计图谱总体上与细胞遗传图谱一致,并进一步将PEPB定位到12q21。