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

被引:28
作者
Arbieva, ZH [1 ]
Banerjee, K
Kim, SY
Edassery, SL
Maniatis, VS
Horrigan, SK
Westbrook, CA
机构
[1] Univ Illinois, Dept Med, Hematol Oncol Sect, Chicago, IL 60607 USA
[2] Univ Illinois, Dept Mol Genet, Chicago, IL 60607 USA
[3] Georgetown Univ, Med Ctr, Vincent T Lombardi Canc Res Ctr, Dept Pediat, Washington, DC 20007 USA
关键词
D O I
10.1101/gr.10.2.244
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A Senomic interval of -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 Pls, 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.
引用
收藏
页码:244 / 257
页数:14
相关论文
共 68 条
  • [1] ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
  • [2] Anbazhagan R, 1998, AM J PATHOL, V152, P815
  • [3] YEAST ARTIFICIAL CHROMOSOME AND RADIATION HYBRID MAP OF LOCI IN CHROMOSOME BAND 8P22, A COMMON REGION OF ALLELIC LOSS IN MULTIPLE HUMAN CANCERS
    BOOKSTEIN, R
    LEVY, A
    MACGROGAN, D
    LEWIS, TB
    WEISSENBACH, J
    OCONNELL, P
    LEACH, RJ
    [J]. GENOMICS, 1994, 24 (02) : 317 - 323
  • [4] Physical mapping of chromosome 8p22 markers and their homozygous deletion in a metastatic prostate cancer
    Bova, GS
    MacGrogan, D
    Levy, A
    Pin, SS
    Bookstein, R
    Isaacs, WB
    [J]. GENOMICS, 1996, 35 (01) : 46 - 54
  • [5] BOVA GS, 1993, CANCER RES, V53, P3869
  • [6] Fluorescence-based sequencing directly from bacterial and P1-derived artificial chromosomes
    Boysen, C
    Simon, MI
    Hood, L
    [J]. BIOTECHNIQUES, 1997, 23 (06) : 978 - &
  • [7] EXON AMPLIFICATION - A STRATEGY TO ISOLATE MAMMALIAN GENES BASED ON RNA SPLICING
    BUCKLER, AJ
    CHANG, DD
    GRAW, SL
    BROOK, JD
    HABER, DA
    SHARP, PA
    HOUSMAN, DE
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (09) : 4005 - 4009
  • [8] A novel interaction between the juxtamembrane region of the p55 tumor necrosis factor receptor and phosphatidylinositol-4-phosphate 5-kinase
    Castellino, AM
    Parker, GJ
    Boronenkov, IV
    Anderson, RA
    Chao, MV
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (09) : 5861 - 5870
  • [9] CHANG FH, 1994, HARMFUL ALGAE NEWS, V8, P1
  • [10] Isolation of 45 exon-like fragments from 8p22->p21.3, a region that is commonly deleted in hepatocellular, colorectal, and non-small cell lung carcinomas
    Chinen, K
    Isomura, M
    Izawa, K
    Fujiwara, Y
    Ohata, H
    Iwamasa, T
    Nakamura, Y
    [J]. CYTOGENETICS AND CELL GENETICS, 1996, 75 (2-3): : 190 - 196