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8p22上前列腺癌缺失区间的高分辨率物理图谱及转录本鉴定

High-resolution physical map and transcript identification of a prostate cancer deletion interval on 8p22.

作者信息

Arbieva Z H, Banerjee K, Kim S Y, Edassery S L, Maniatis V S, Horrigan S K, Westbrook C A

机构信息

Section of Hematology-Oncology, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois 60607-7170 USA.

出版信息

Genome Res. 2000 Feb;10(2):244-57. doi: 10.1101/gr.10.2.244.

Abstract

A genomic interval of approximately 1-1.5 Mb centered at the MSR marker on 8p22 has emerged as a possible site for a tumor suppressor gene, based on high rates of allele loss and the presence of a homozygous deletion found in metastatic prostate cancer. The objective of this study was to prepare a bacterial contig of this interval, integrate the contig with radiation hybrid (RH) databases, and use these resources to identify transcription units that might represent the candidate tumor suppressor genes. Here we present a complete bacterial contig across the interval, which was assembled using 22 published and 17 newly originated STSs. The physical map provides twofold or greater coverage over much of the interval, including 17 BACs, 15 P1s, 2 cosmids, and 1 PAC clone. The position of the selected markers across the interval in relation to the other markers on the larger chromosomal scale was confirmed by RH mapping using the Stanford G3 RH panel. Transcribed units within the deletion region were identified by exon amplification, searching of the Human Transcript Map, placement of unmapped expressed sequence tags (ESTs) from the Radiation Hybrid Database (RHdb), and from other published sources, resulting in the isolation of six unique expressed sequences. The transcript map of the deletion interval now includes two known genes (MSR and N33) and six novel ESTs.

摘要

基于转移性前列腺癌中较高的等位基因缺失率和纯合缺失的存在,位于8号染色体短臂22区带MSR标记中心、长度约为1 - 1.5 Mb的基因组区间已成为肿瘤抑制基因的一个可能位点。本研究的目的是构建该区间的细菌重叠群,将该重叠群与辐射杂种(RH)数据库整合,并利用这些资源鉴定可能代表候选肿瘤抑制基因的转录单元。在此,我们展示了跨越该区间的完整细菌重叠群,它是利用22个已发表的和17个新产生的序列标签位点(STS)组装而成的。物理图谱在该区间的大部分区域提供了两倍或更高的覆盖率,包括17个细菌人工染色体(BAC)、15个P1噬菌体、2个黏粒和1个P1人工染色体(PAC)克隆。通过使用斯坦福G3 RH板进行RH定位,确认了该区间内所选标记相对于更大染色体尺度上其他标记的位置。通过外显子扩增、搜索人类转录图谱、在辐射杂种数据库(RHdb)以及其他已发表来源中定位未映射的表达序列标签(EST),鉴定了缺失区域内的转录单元,从而分离出6个独特的表达序列。缺失区间的转录图谱现在包括两个已知基因(MSR和N33)以及6个新的EST。

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