A HUMAN HOMOLOG OF THE DROSOPHILA POLARITY GENE FRIZZLED HAS BEEN IDENTIFIED AND MAPPED TO 17Q21.1

被引:47
作者
ZHAO, ZY
LEE, CC
BALDINI, A
CASKEY, CT
机构
[1] BAYLOR COLL MED,HOWARD HUGHES MED INST,HOUSTON,TX 77030
[2] BAYLOR COLL MED,CLAYTON FDN RES,HOUSTON,TX 77030
关键词
D O I
10.1006/geno.1995.1060
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
The frizzled (fz) locus in Drosophila is required for the transmission of polarity signals across the plasma membrane in epidermal cells, as well as to their neighboring cells in the developing wing. The identification of a tissue polarity gene from the fz locus in Drosophila melanogaster has been reported. The fz gene encodes a protein (Fz) with seven putative transmembrane domains, which was suggested to function as a G-protein-coupled receptor. Here we report the identification of a human homologue for the fz gene (FZD2). The FZD2 gene was isolated from a human ovarian cDNA library and mapped to 17q21.1 by fluorescent in situ hybridization (FISH) with a corresponding cosmid. The full-length cDNA of human FZD2 encodes a protein (FZD-2) of 565 amino acids that shares 56% sequence identity with Drosophila Fz. The expression of the FZD2 gene seems to be developmentally regulated, with high levels of expression in fetal kidney and lung and in adult colon and ovary. The structure of FZD-2 suggests that it has a role in transmembrane signal transmission, although its precise physiological function and associated pathways are yet to be determined. (C) 1995 Academic Press, Inc.
引用
收藏
页码:370 / 373
页数:4
相关论文
共 9 条
  • [1] BROOK JD, 1992, CELL, V69, P784
  • [2] CHAN SDH, 1992, J BIOL CHEM, V267, P25202
  • [3] VARIATION OF THE CGG REPEAT AT THE FRAGILE-X SITE RESULTS IN GENETIC INSTABILITY - RESOLUTION OF THE SHERMAN PARADOX
    FU, YH
    KUHL, DPA
    PIZZUTI, A
    PIERETTI, M
    SUTCLIFFE, JS
    RICHARDS, S
    VERKERK, AJMH
    HOLDEN, JJA
    FENWICK, RG
    WARREN, ST
    OOSTRA, BA
    NELSON, DL
    CASKEY, CT
    [J]. CELL, 1991, 67 (06) : 1047 - 1058
  • [4] ANDROGEN RECEPTOR GENE-MUTATIONS IN X-LINKED SPINAL AND BULBAR MUSCULAR-ATROPHY
    LASPADA, AR
    WILSON, EM
    LUBAHN, DB
    HARDING, AE
    FISCHBECK, KH
    [J]. NATURE, 1991, 352 (6330) : 77 - 79
  • [5] MYOTONIC-DYSTROPHY MUTATION - AN UNSTABLE CTG REPEAT IN THE 3' UNTRANSLATED REGION OF THE GENE
    MAHADEVAN, M
    TSILFIDIS, C
    SABOURIN, L
    SHUTLER, G
    AMEMIYA, C
    JANSEN, G
    NEVILLE, C
    NARANG, M
    BARCELO, J
    OHOY, K
    LEBLOND, S
    EARLEMACDONALD, J
    DEJONG, PJ
    WIERINGA, B
    KORNELUK, RG
    [J]. SCIENCE, 1992, 255 (5049) : 1253 - 1255
  • [6] IDENTIFICATION OF A GENE (FMR-1) CONTAINING A CGG REPEAT COINCIDENT WITH A BREAKPOINT CLUSTER REGION EXHIBITING LENGTH VARIATION IN FRAGILE-X SYNDROME
    VERKERK, AJMH
    PIERETTI, M
    SUTCLIFFE, JS
    FU, YH
    KUHL, DPA
    PIZZUTI, A
    REINER, O
    RICHARDS, S
    VICTORIA, MF
    ZHANG, FP
    EUSSEN, BE
    VANOMMEN, GJB
    BLONDEN, LAJ
    RIGGINS, GJ
    CHASTAIN, JL
    KUNST, CB
    GALJAARD, H
    CASKEY, CT
    NELSON, DL
    OOSTRA, BA
    WARREN, ST
    [J]. CELL, 1991, 65 (05) : 905 - 914
  • [7] A DROSOPHILA TISSUE POLARITY LOCUS ENCODES A PROTEIN CONTAINING 7 POTENTIAL TRANSMEMBRANE DOMAINS
    VINSON, CR
    CONOVER, S
    ADLER, PN
    [J]. NATURE, 1989, 338 (6212) : 263 - 264
  • [8] DIRECTIONAL NON-CELL AUTONOMY AND THE TRANSMISSION OF POLARITY INFORMATION BY THE FRIZZLED GENE OF DROSOPHILA
    VINSON, CR
    ADLER, PN
    [J]. NATURE, 1987, 329 (6139) : 549 - 551
  • [9] CLINICAL, CYTOGENETIC, AND MOLECULAR EVIDENCE FOR AN INFANT WITH SMITH-MAGENIS SYNDROME BORN FROM A MOTHER HAVING A MOSAIC 17P11.2P12 DELETION
    ZORI, RT
    LUPSKI, JR
    ZHANG, HJ
    GREENBERG, F
    KILLIAN, JM
    GRAY, BA
    DRISCOLL, DJ
    PATEL, PI
    ZACKOWSKI, JL
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 47 (04): : 504 - 511