Identification of a third EXT-like gene (EXTL3) belonging to the EXT gene family

被引:117
作者
Van Hul, W
Wuyts, W
Hendrickx, J
Speleman, F
Wauters, J
De Boulle, K
Van Roy, N
Bossuyt, P
Willems, PJ
机构
[1] Univ Antwerp, Dept Med Genet, B-2610 Antwerp, Belgium
[2] Univ Ghent, Dept Med Genet, B-9000 Ghent, Belgium
关键词
D O I
10.1006/geno.1997.5101
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Two homologous genes, EXT1 and EXTS, responsible for the development of benign multiple cartilagenous bone tumors (exostoses) on the long bones, have been identified in the past 2 years. Several arguments have been provided to support the hypothesis that these genes have tumor suppressor activity and that loss of function of these genes may contribute to the development of bone tumors. The recent identification of two EXT-like genes, EXTL1 and EXTL2, homologous to the EXT genes and to each other, revealed the existence of a larger family of genes. We now report the identification of a homologous EST (EST01365), not derived from the known EXT and EXTL genes, indicating the existence of one additional member of this gene family. We characterized this third EXT-like gene, EXTL3, and compared it with the other four members of the EXT-EXTL family. In view of its putative tumor suppressor function, the EXTL3 gene can be considered a candidate gene for the breast cancer locus on chromosome 8p12-p22. (C) 1998 Academic Press.
引用
收藏
页码:230 / 237
页数:8
相关论文
共 42 条
  • [1] AHN J, 1995, NAT GENET, V11, P187
  • [2] Altschul SF, 1996, METHOD ENZYMOL, V266, P460
  • [3] [Anonymous], [No title captured]
  • [4] MAPPING THE GENE FOR HEREDITARY CUTANEOUS MALIGNANT-MELANOMA DYSPLASTIC NEVUS TO CHROMOSOME-1P
    BALE, SJ
    DRACOPOLI, NC
    TUCKER, MA
    CLARK, WH
    FRASER, MC
    STANGER, BZ
    GREEN, P
    DONISKELLER, H
    HOUSMAN, DE
    GREENE, MH
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1989, 320 (21) : 1367 - 1372
  • [5] Blanton SH, 1996, AM J MED GENET, V62, P150
  • [6] BIOLOGIC AND CLINICAL-SIGNIFICANCE OF CYTOGENETIC AND MOLECULAR CYTOGENETIC ABNORMALITIES IN BENIGN AND MALIGNANT CARTILAGINOUS LESIONS
    BRIDGE, JA
    BHATIA, PS
    ANDERSON, JR
    NEFF, JR
    [J]. CANCER GENETICS AND CYTOGENETICS, 1993, 69 (02) : 79 - 90
  • [7] EVIDENCE FOR 2 TUMOR-SUPPRESSOR LOCI ON CHROMOSOMAL BANDS-1P35-36 INVOLVED IN NEUROBLASTOMA - ONE PROBABLY IMPRINTED, ANOTHER ASSOCIATED WITH N-MYC AMPLIFICATION
    CARON, H
    PETER, M
    VANSLUIS, P
    SPELEMAN, F
    DEKRAKER, J
    LAUREYS, G
    MICHON, J
    BRUGIERES, L
    VOUTE, PA
    WESTERVELD, A
    SLATER, R
    DELATTRE, O
    VERSTEEG, R
    [J]. HUMAN MOLECULAR GENETICS, 1995, 4 (04) : 535 - 539
  • [8] COOK A, 1993, AM J HUM GENET, V53, P71
  • [9] GENETIC IDENTIFICATION OF MOM-1, A MAJOR MODIFIER LOCUS AFFECTING MIN-INDUCED INTESTINAL NEOPLASIA IN THE MOUSE
    DIETRICH, WF
    LANDER, ES
    SMITH, JS
    MOSER, AR
    GOULD, KA
    LUONGO, C
    BORENSTEIN, N
    DOVE, W
    [J]. CELL, 1993, 75 (04) : 631 - 639
  • [10] Eddy S R, 1995, J Comput Biol, V2, P9, DOI 10.1089/cmb.1995.2.9