Tsui L C, Rommens J M, Burns J, Zengerling S, Riordan J R, Carlock L R, Grzeschik K H, Buchwald M
Department of Genetics, Hospital for Sick Children, Toronto, Ontario, Canada.
Philos Trans R Soc Lond B Biol Sci. 1988 Jun 15;319(1194):263-73. doi: 10.1098/rstb.1988.0048.
Genetic linkage analysis with polymorphic DNA markers (restriction fragment length polymorphisms: RFLPS) has allowed the assignment of the cystic fibrosis (CF) locus to the long arm of chromosome 7, within the region of band q31. Two of these markers, MET and D7S8, are tightly linked to the disease locus. Although recent data suggest that they are located on opposite sides of CF, the two can be separated by as much as 5 centimorgans. To obtain a better description of the CF locus and, eventually, to identify the affected gene, additional DNA markers are required to connect MET and D7S8, physically. We have screened the flow-sorted chromosome-7-specific library and thus far isolated 28 new probes from the 7q31 region by DNA hybridization analysis that uses a series of somatic cell hybrids containing various portions of human chromosome 7. Together with the previously identified markers, MET, D7S8, D7S13 and D7S16, these new markers should provide a fine genetic and physical map for the chromosomal region surrounding CF. DNA segments can then be sequentially cloned by chromosome walking from points closest to the CF locus and examined for genes that are preferentially expressed in tissues known to be affected in the disease.
利用多态性DNA标记(限制性片段长度多态性:RFLP)进行的遗传连锁分析已将囊性纤维化(CF)基因座定位于7号染色体长臂的q31带区域内。其中两个标记,MET和D7S8,与疾病基因座紧密连锁。尽管最近的数据表明它们位于CF的两侧,但两者之间的距离可达5厘摩。为了更好地描述CF基因座,并最终鉴定出受影响的基因,需要额外的DNA标记来在物理上连接MET和D7S8。我们筛选了经流式细胞仪分选的7号染色体特异性文库,到目前为止,通过DNA杂交分析,利用一系列含有人类7号染色体不同部分的体细胞杂种,从7q31区域分离出了28个新探针。连同先前鉴定的标记MET、D7S8、D7S13和D7S16,这些新标记应为CF周围的染色体区域提供精细的遗传和物理图谱。然后可以通过染色体步移从最接近CF基因座的点开始依次克隆DNA片段,并检测在已知受该疾病影响的组织中优先表达的基因。