Bardenheuer W, Michaelis S, Lux A, Vieten L, Bröcker F, Jülicher K, Willers C, Siebert R, Smith D I, van der Hout A H, Buys C, Schütte J, Opalka B
Innere Klinik und Poliklinik (Tumorforschung), Universitätsklinikum Essen, Germany.
Genome Res. 1996 Mar;6(3):176-86. doi: 10.1101/gr.6.3.176.
Chromosomal deletions and translocations of human chromosome region 3p14 are observed in various human malignancies and suggest the existence of a tumor suppressor gene locus within this region. Tumors most frequently affected by these aberrations are small-cell lung cancer and renal-cell carcinoma. In continuation of our previously published YAC contig of chromosome region 3p14.2-p14.3, we report here on the construction of a YAC contig of at least 11 Mb that consisted of 171 YACs and covers the entire subregion 3p14.1. This contig includes the t(3;8) breakpoint of a hereditary renal-cell carcinoma localized in 3p14.2 and extends into human chromosome region 3p12-p13. It defines the order of 34 DNA probes in relation to reference markers D3S6 and D3S30 as well as the human protein tyrosine phosphatase-gamma gene. For 31 DNA probes we identified nonchimeric YACs by fluorescence in situ hybridization. The minimal tilling pathway consists of 16 yeast artificial chromosomes. As a prerequisite for identification of a putative tumor suppressor gene within this region, this contig renders human chromosome region 3p14.1 accessible to gene isolation.
在多种人类恶性肿瘤中均观察到人类染色体区域3p14的染色体缺失和易位,这表明该区域内存在一个肿瘤抑制基因位点。受这些畸变影响最频繁的肿瘤是小细胞肺癌和肾细胞癌。在我们之前发表的关于染色体区域3p14.2 - p14.3的酵母人工染色体(YAC)重叠群的基础上,我们在此报告构建了一个至少11兆碱基(Mb)的YAC重叠群,它由171个YAC组成,覆盖了整个3p14.1亚区域。这个重叠群包括一个位于3p14.2的遗传性肾细胞癌的t(3;8)断点,并延伸到人类染色体区域3p12 - p13。它确定了34个DNA探针相对于参考标记D3S6和D3S30以及人类蛋白酪氨酸磷酸酶γ基因的顺序。对于31个DNA探针,我们通过荧光原位杂交鉴定出了非嵌合YAC。最小拼接路径由16个酵母人工染色体组成。作为在该区域鉴定假定肿瘤抑制基因的前提条件,这个重叠群使得人类染色体区域3p14.1可用于基因分离。