Human BAC Contig Covering the Deleted Region in Pancreatic Cancer at 12q21

E. Youssef, K. Kaneko, T. Yatsuoka, Y. Hayashi, M. Hoshi, A. Horii, T. Furukawa
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引用次数: 5

Abstract

In sporadic human primary pancreatic cancer tissues, loss of heterozygosity is frequently observed in the 1-cM region between D12S81 and D12S1719 at 12q21. Loss of this chromosome arm is known to be associate with a poor prognosis in pancreatic cancer patients. Herein we report a complete contig of human bacterial artificial chromosome (BAC) clones covering the deleted region. The region was covered by 21 BAC clones in a minimum tiling path. The clones were confirmed to exist at 12q21 by fluorescence In situ hybridization. We identified novel 40 sequence tagged sites and mapped 10 expressed sequence tags in this region. The BAC contig reported here provides an avenue for determining the complete nucleotide sequence and mining putative tumor suppressor genes in the deleted region of pancreatic cancer at 12q21.
人类BAC序列覆盖胰腺癌12q21缺失区域
在散发性人原发性胰腺癌组织中,在12q21的D12S81和D12S1719之间的1-cM区域经常观察到杂合性缺失。已知这条染色体臂的缺失与胰腺癌患者预后不良有关。在这里,我们报告了一个完整的人类细菌人工染色体(BAC)克隆组覆盖缺失区域。在最小平铺路径上,该区域被21个BAC克隆覆盖。通过荧光原位杂交证实该克隆存在于12q21位点。我们发现了40个新的序列标记位点,并在该区域绘制了10个表达的序列标记。本文报道的BAC序列为确定胰腺癌12q21缺失区域的完整核苷酸序列和挖掘推定的肿瘤抑制基因提供了途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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