Eccles M R, Millow L J, Wilkins R J, Reeve A E
Hum Genet. 1984;67(2):190-2. doi: 10.1007/BF00272999.
We have examined the chromosomes from a case of sporadic Wilms' tumor using in situ hybridization to determine whether the Ha-ras (c-Ha-ras 1) oncogene had been deleted as the result of a reciprocal chromosomal translocation between the short arm of chromosome 11 (breakpoint 11p13) and the long arm of chromosome 12 (breakpoint 12q13). Neither the derivative 11 nor derivative 12 chromosome hybridized significantly to the Ha-ras probe, which indicated that this cellular oncogene was deleted as a consequence of the translocation. This conclusion is supported by a Southern blot analysis which demonstrates loss of a Harvey-ras allele. These results support the view that the Ha-ras oncogene may be functionally involved in Wilms' tumor development.
我们使用原位杂交技术检测了一例散发性肾母细胞瘤的染色体,以确定Ha-ras(c-Ha-ras 1)癌基因是否因11号染色体短臂(断点11p13)与12号染色体长臂(断点12q13)之间的相互染色体易位而缺失。11号衍生染色体和12号衍生染色体均未与Ha-ras探针发生明显杂交,这表明该细胞癌基因因易位而缺失。Southern印迹分析证实了Harvey-ras等位基因的缺失,支持了这一结论。这些结果支持了Ha-ras癌基因可能在肾母细胞瘤发生过程中发挥功能作用的观点。