Negrini M, Sabbioni S, Ohta M, Veronese M L, Rattan S, Junien C, Croce C M
Jefferson Cancer Institute, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.
Cancer Res. 1995 Jul 1;55(13):2904-9.
Genetic alterations of chromosome region 11p15 have been detected in neoplastic diseases as well as in cancer-predisposing syndromes. The cloning of the entire chromosomal region will be important for the identification and characterization of critical tumor suppressor genes. We have developed a yeast artificial chromosome contig that covers up to 7 Mb of this chromosome band. The most centromeric marker included in the contig is D11S932 and the most telomeric is D11S470. We have developed 18 new STS markers, which have been located in the contig in relation to 16 known markers. One of the yeast artificial chromosome clones was found to span the chromosome 11 breakpoint of the translocation t(11;18), associated with a case of Beckwith-Wiedemann syndrome. Cloning the regions in proximity to this translocation might reveal the presence of a gene altered in association with the development of Beckwith-Wiedemann syndrome.
在肿瘤性疾病以及癌症易感综合征中已检测到染色体区域11p15的基因改变。克隆整个染色体区域对于关键肿瘤抑制基因的鉴定和表征至关重要。我们构建了一个酵母人工染色体重叠群,其覆盖该染色体带多达7兆碱基。重叠群中包含的最靠近着丝粒的标记是D11S932,最靠近端粒的是D11S470。我们开发了18个新的序列标签位点(STS)标记,它们已相对于16个已知标记定位在重叠群中。发现一个酵母人工染色体克隆跨越了与1例贝克威思-维德曼综合征相关的t(11;18)易位的11号染色体断点。克隆该易位附近的区域可能会揭示与贝克威思-维德曼综合征发生相关的一个改变的基因的存在。