Bufton L, Mohandas T K, Magenis R E, Sheehy R, Bestwick R K, Litt M
Hum Genet. 1986 Dec;74(4):425-31. doi: 10.1007/BF00280499.
A cosmid library was constructed from genomic DNA of a human-mouse somatic cell hybrid containing an 11q-16q translocation chromosome as the only human DNA. Cosmids with human inserts were prehybridized with total human DNA and were screened to find probes that revealed highly polymorphic loci. From one such cosmid, CF33-79, a single-copy subclone was isolated which revealed an insertion/deletion polymorphism with at least 11 alleles and a PIC of 0.77. Using a somatic cell hybrid mapping panel, the subclone was mapped to chromosome 16. By in situ hybridization with the entire cosmid used as a probe, chromosomal localization was shown at 16q22----24.
用含有11q - 16q易位染色体作为唯一人类DNA的人 - 鼠体细胞杂种的基因组DNA构建了一个黏粒文库。将含有人插入片段的黏粒与人总DNA进行预杂交,并进行筛选以找到揭示高度多态性位点的探针。从一个这样的黏粒CF33 - 79中分离出一个单拷贝亚克隆,该亚克隆揭示了一个具有至少11个等位基因且杂合度信息含量(PIC)为0.77的插入/缺失多态性。使用体细胞杂种定位板,将该亚克隆定位到16号染色体上。通过用整个黏粒作为探针进行原位杂交,显示染色体定位在16q22----24。