Seawright A, Fletcher J M, Fantes J A, Morrison H, Porteous D J, Li S S, Hastie N D, Van Heyningen V
MRC Clinical and Population Cytogenetics Unit, Western General Hospital, Edinburgh, U.K.
Somat Cell Mol Genet. 1988 Jan;14(1):21-30. doi: 10.1007/BF01535046.
We used the fluorescence-activated cell sorter (FACS) to select a series of somatic cell hybrids with deleted or translocated chromosome 11 segregated from its normal homolog. Analysis of these cell hybrids with gene-specific probes and for cell-surface marker expression has allowed us to order the markers and define a smallest region of overlap (SRO) for deletions associated with the WAGR (Wilms' tumor, aniridia, genitourinary abnormalities, and mental retardation) region of chromosome 11. Two translocation breakpoints in 11p13 (one associated with familial aniridia and one with a sporadic case of congenital renal dysfunction resulting from urethral and ureteral atresia) map within this SRO.
我们使用荧光激活细胞分选仪(FACS)从其正常同源染色体中分离出一系列11号染色体缺失或易位的体细胞杂种。用基因特异性探针分析这些细胞杂种并检测细胞表面标志物表达,使我们能够对标志物进行排序,并确定与11号染色体WAGR(威尔姆斯瘤、无虹膜、泌尿生殖系统异常和智力迟钝)区域相关缺失的最小重叠区域(SRO)。11p13中的两个易位断点(一个与家族性无虹膜相关,另一个与因尿道和输尿管闭锁导致的先天性肾功能不全散发病例相关)定位于此SRO内。