A gene for familial juvenile polyposis maps to chromosome 18q21.1

被引:74
作者
Howe, JR
Ringold, JC
Summers, RW
Mitros, FA
Nishimura, DY
Stone, EM
机构
[1] Univ Iowa, Coll Med, Dept Surg, Iowa City, IA 52242 USA
[2] Univ Iowa, Coll Med, Dept Med, Iowa City, IA 52242 USA
[3] Univ Iowa, Coll Med, Dept Pathol, Iowa City, IA 52242 USA
[4] Univ Iowa, Coll Med, Dept Pediat, Iowa City, IA 52242 USA
[5] Univ Iowa, Coll Med, Dept Ophthalmol, Iowa City, IA 52242 USA
关键词
D O I
10.1086/301840
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Familial juvenile polyposis (FJP) is a hamartomatous polyposis syndrome in which affected family members develop upper and lower gastrointestinal juvenile polyps and are at increased risk for gastrointestinal cancer. A genetic locus for FJP has not yet been identified by linkage; therefore, the objective of this study was to perform a focused genome screen in a large family segregating FJP. No evidence for linkage was found with markers near MSH2, MLH1, MCC, APC, HMPS, CDLM2A, JP1, PTEN, KRAS2 TP53, or LKB1. Linkage to FJP was established with several markers from chromosome 18q21.1. The maximum LOD score was 5.00, with marker D18S1099 (recombination fraction of .001). Analysis of critical recombinants places the FJP gene in an 11.9-cM interval bounded by D18S1118 and D18S487, a region that also contains the tumor-suppressor genes DCC and DPC4. These data demonstrate localization of a gene for FJP to chromosome 18q21.1 by linkage, and they raise the possibility that either DCC or DPC4 could be responsible for FJP.
引用
收藏
页码:1129 / 1136
页数:8
相关论文
共 55 条
  • [1] COEXISTING JUVENILE POLYPS AND TUBULOVILLOUS ADENOMA OF COLON WITH CARCINOMA INSITU - REPORT OF A CASE
    BAPTIST, SJ
    SABATINI, MT
    [J]. HUMAN PATHOLOGY, 1985, 16 (10) : 1061 - 1063
  • [2] FAST AND SENSITIVE SILVER STAINING OF DNA IN POLYACRYLAMIDE GELS
    BASSAM, BJ
    CAETANOANOLLES, G
    GRESSHOFF, PM
    [J]. ANALYTICAL BIOCHEMISTRY, 1991, 196 (01) : 80 - 83
  • [3] BENTLEY E, 1989, AM J GASTROENTEROL, V84, P1456
  • [4] HUMAN SSAV-RELATED ENDOGENOUS RETROVIRAL ELEMENT - LTR-LIKE SEQUENCE AND CHROMOSOMAL LOCALIZATION TO 18Q21
    BRACKWERNER, R
    BARTON, DE
    WERNER, T
    FOELLMER, BE
    LEIBMOSCH, C
    FRANCKE, U
    ERFLE, V
    HEHLMANN, R
    [J]. GENOMICS, 1989, 4 (01) : 68 - 75
  • [5] BURT RW, 1990, B WORLD HEALTH ORGAN, V68, P655
  • [6] THE DCC GENE - STRUCTURAL-ANALYSIS AND MUTATIONS IN COLORECTAL CARCINOMAS
    CHO, KR
    OLINER, JD
    SIMONS, JW
    HEDRICK, L
    FEARON, ER
    PREISINGER, AC
    HEDGE, P
    SILVERMAN, GA
    VOGELSTEIN, B
    [J]. GENOMICS, 1994, 19 (03) : 525 - 531
  • [7] COTTINGHAM RW, 1993, AM J HUM GENET, V53, P252
  • [8] Molecular classification of the inherited hamartoma polyposis syndromes: Clearing the muddied waters
    Eng, C
    Ji, HL
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (05) : 1020 - 1022
  • [9] MADR2 maps to 18q21 and encodes a TGF beta-regulated MAD-related protein that is functionally mutated in colorectal carcinoma
    Eppert, K
    Scherer, SW
    Ozcelik, H
    Pirone, R
    Hoodless, P
    Kim, H
    Tsui, LC
    Bapat, B
    Gallinger, S
    Andrulis, IL
    Thomsen, GH
    Wrana, JL
    Attisano, L
    [J]. CELL, 1996, 86 (04) : 543 - 552
  • [10] Phenotype of mice lacking functional Deleted in colorectal cancer (Dcc) gene
    Fazeli, A
    Dickinson, SL
    Hermiston, ML
    Tighe, RV
    Steen, RG
    Small, CG
    Stoeckli, ET
    KeinoMasu, K
    Masu, M
    Rayburn, H
    Simons, J
    Bronson, RT
    Gordon, JI
    TessierLavigne, M
    Weinberg, RA
    [J]. NATURE, 1997, 386 (6627) : 796 - 804