Hoggard N, Hey Y, Brintnell B, James L, Jones D, Mitchell E, Weissenbach J, Varley J M
CRC Department of Cancer Genetics, Paterson Institute for Cancer Research, Manchester, United Kingdom.
Genomics. 1995 Nov 20;30(2):233-43. doi: 10.1006/geno.1995.9882.
We have mapped a region of high loss of heterozygosity in breast cancer to a 2-cM interval between the loci D1S430 and D1S465 on chromosome 1p31.1. This region shows allelic imbalance in around 60% of breast tumors. As part of a strategy to clone the target gene(s) within this interval, we have generated a yeast artificial chromosome contig spanning over 7 Mb. YACs from the CEPH and Zeneca (formerly ICI) libraries have been obtained by screening with PCR-based STSs from the region for both previously identified loci and newly isolated STSs. The YACs have been assembled into a contig by a combination of approaches, including analysis of their STS content, generation of new STSs from the ends of key YACs, and long-range restriction mapping. These YAC clones provide the basis for complete characterization of the region of high loss in breast cancer and for the ultimate identification of the target gene(s).
我们已经将乳腺癌中杂合性高缺失区域定位到1号染色体p31.1上基因座D1S430和D1S465之间2厘摩的区间。该区域在约60%的乳腺肿瘤中显示出等位基因失衡。作为在这个区间内克隆目标基因策略的一部分,我们构建了一个跨越7兆碱基的酵母人工染色体重叠群。通过用该区域基于PCR的序列标签位点(STS)筛选先前鉴定的基因座和新分离的STS,从CEPH和捷利康(原帝国化学工业公司)文库中获得了酵母人工染色体。通过多种方法的组合,包括分析它们的STS含量、从关键酵母人工染色体末端产生新的STS以及进行长距离限制性图谱分析,将这些酵母人工染色体组装成了一个重叠群。这些酵母人工染色体克隆为全面表征乳腺癌高缺失区域以及最终鉴定目标基因奠定了基础。