Sanson M, Zhang F, Demczuk S, Delattre O, DeJong P, Aurias A, Thomas G, Rouleau G A
Centre for Research in Neuroscience, McGill University, Montreal, Canada.
Genomics. 1993 Sep;17(3):776-9. doi: 10.1006/geno.1993.1407.
Fifty-nine NotI linking clones have been isolated from a flow-sorted chromosome 22 cosmid library and mapped using fluorescence in situ hybridization and/or a panel of somatic cell hybrids. Fourteen clones map to the short arm of chromosome 22, 31 to the long arm, and 9 to other chromosomes; 5 clones could not be unambiguously mapped. To identify potentially informative genetic markers, the chromosome 22 clones were screened for poly(CA) sequences; 24 positively hybridizing clones, 10 on the long arm and 14 on the short arm, were identified. These clones will be useful for constructing a long-range restriction map of chromosome 22 and may facilitate the cloning of chromosome 22 genes.
已从一个经流式细胞分选的22号染色体黏粒文库中分离出59个NotI连接克隆,并使用荧光原位杂交和/或一组体细胞杂种进行了定位。14个克隆定位于22号染色体短臂,31个定位于长臂,9个定位于其他染色体;5个克隆无法明确定位。为了鉴定潜在的信息性遗传标记,对22号染色体克隆进行了多聚(CA)序列筛选;鉴定出24个阳性杂交克隆,其中10个位于长臂,14个位于短臂。这些克隆将有助于构建22号染色体的长程限制性图谱,并可能促进22号染色体基因的克隆。