Cloning of the human homolog of conductin (AXIN2), a gene mapping to chromosome 17q23-q24

被引:58
|
作者
Mai, M
Qian, CP
Yokomizo, A
Smith, DI
Liu, WG
机构
[1] Mayo Clin & Mayo Fdn, Dept Lab Med & Pathol, Div Expt Pathol, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Dept Urol Res, Rochester, MN 55905 USA
关键词
D O I
10.1006/geno.1998.5650
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
Conductin or Axil, an Axin homolog, plays an important role in the regulation of beta-catenin stability in the Wnt signaling pathway. To facilitate the molecular analysis of the human gene, we isolated the human homolog, AXIN2. The cDNA contains a 2529-bp open reading frame and encodes a putative protein of 843 amino acids. Compared with rat and mouse homologs, AXIN2 shows an overall 89% amino acid identity. Several functional domains in this protein are highly conserved including the GRS (95.9%), GSK-3 beta (96.3%), Dsh (98%), and beta-catenin (89.9%) domains. Radiation hybrid mapping localized the AXIN2 gene to human chromosome 17q23-q24, a region that shows frequent loss of heterozygosity in breast cancer, neuroblastoma, and other tumors. Human AXIN2 is thus a very strong candidate involved in multiple tumor types. (C) 1999 Academic Press.
引用
收藏
页码:341 / 344
页数:4
相关论文
共 50 条
  • [1] Genomic structure, chromosome mapping and expression analysis of the human AXIN2 gene
    Dong, X
    Seelan, RS
    Qian, C
    Mai, M
    Liu, W
    CYTOGENETICS AND CELL GENETICS, 2001, 93 (1-2): : 26 - 28
  • [2] Construction of a detailed physical and transcript map of the candidate region for Russell-Silver syndrome on chromosome 17q23-q24
    Dörr, S
    Midro, AT
    Färber, C
    Giannakudis, J
    Hansmann, I
    GENOMICS, 2001, 71 (02) : 174 - 181
  • [3] Cloning and mapping of the UNC5C gene to human chromosome 4q21-q23
    Ackerman, SL
    Knowles, BB
    GENOMICS, 1998, 52 (02) : 205 - 208
  • [4] Cloning of the cDNA for a human homolog of the rat PEP-19 gene and mapping to chromosome 21q22.2-q22.3
    Chen, HM
    Bouras, C
    Antonarakis, SE
    HUMAN GENETICS, 1996, 98 (06) : 672 - 677
  • [5] A physical and transcription map of the candidate region 17q23-q24 for a gene causing Russell-Silver syndrome (RSS).
    Doerr, S
    Midro, AT
    Giannakudis, J
    Hansmann, I
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 272 - 272
  • [6] Positional cloning of Bipolar susceptibility gene in the Darier region of chromosome 12q23-q24
    Craddock, N
    Glaser, B
    Green, E
    O'Donovan, MC
    Jones, I
    Owen, MJ
    Jones, I
    AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 105 (07): : 590 - 590
  • [7] Positional cloning of bipolar susceptibility gene in the Darier region of chromosome 12q23-q24
    Craddock, N
    Glaser, B
    Green, E
    Jacobsen, N
    Elvidge, G
    Kirov, G
    Lendon, C
    O'Donovan, M
    Jones, I
    Owen, M
    AMERICAN JOURNAL OF MEDICAL GENETICS, 2002, 114 (07): : 719 - 719
  • [8] MAPPING OF THE GENE FOR DOMINANT PALMOPLANTARIS HYPERKERATOSIS (TYLOSIS) ON CHROMOSOME 17Q12-Q24
    ROGAEV, EI
    ROGAEVA, EA
    GINTER, EK
    KOROVAITSEVA, GI
    FARRER, LA
    SHLENSKII, AB
    PRYTKOV, AN
    STGEORGEHYSLOP, PH
    MORDOVTSEV, VN
    GENETIKA, 1994, 30 (03): : 326 - 329
  • [9] EVOLUTIONARY CONSERVATION OF THE EPS8 GENE AND ITS MAPPING TO HUMAN-CHROMOSOME 12Q23-Q24
    WONG, WT
    CARLOMAGNO, F
    DRUCK, T
    BARLETTA, C
    CROCE, CM
    HUEBNER, K
    KRAUS, MH
    DIFIORE, PP
    ONCOGENE, 1994, 9 (10) : 3057 - 3061
  • [10] ASSIGNMENT OF THE HUMAN MYELOPEROXIDASE GENE TO Q21.3-Q23 BANDS OF CHROMOSOME-17
    ABE, T
    INAZAWA, J
    INOUE, K
    CYTOGENETICS AND CELL GENETICS, 1989, 51 (1-4): : 948 - 948