A family of putative tumor suppressors is structurally and functionally conserved in humans and yeast

被引:141
作者
Li, LW
Ernsting, BR
Wishart, MJ
Lohse, DL
Dixon, JE
机构
[1] UNIV MICHIGAN, DEPT BIOL CHEM, ANN ARBOR, MI 48109 USA
[2] UNIV MICHIGAN, DEPT PHYSIOL, ANN ARBOR, MI 48109 USA
关键词
D O I
10.1074/jbc.272.47.29403
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
In Saccharomyces cerevisiae the CDC14 gene is essential for cell cycle progression, Strains carrying the cdc14-1(ts) allele enter the cell cycle and arrest at restrictive temperatures, We have identified two human cDNAs encoding proteins which share sequence identity to the yeast CDC14p. The cell cycle arrest in cdc14-1(ts) can be specifically complemented by the human cDNAs suggesting that they are functionally equivalent to the yeast CDC14 gene, Another clone identified in the search for human CDC14-like proteins corresponded to the putative tumor suppressor gene PTEN/MMAC1 (phosphatase and tensin homologue deleted on chromo same 10 or mutated in multiple advanced cancers 1), Analysis of the PTEN/MMAC1 showed that it did not complement the cdc14-1(ts) allele and that it is more closely related to the yeast open reading frame YNL128W. Human CDC14p and PTEN/MMAC1 were expressed as recombinant proteins, and both were shown to have kinetic properties characteristic of dual specific phosphatases, The human CDC14p was localized in the nucleus while PTEN/MMAC1 has been reported to be localized in the cytoplasm, Our results suggest that CDC14 and YNL128W/PTEN/MMAC1 represent two related, but distinct, families of human and yeast phosphatases.
引用
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页码:29403 / 29406
页数:4
相关论文
共 16 条
  • [1] ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
  • [2] Ernsting BR, 1997, J BIOL CHEM, V272, P9332
  • [3] Kinetic analysis of the catalytic domain of human Cdc25B
    Gottlin, EB
    Xu, X
    Epstein, DM
    Burke, SP
    Eckstein, JW
    Ballou, DP
    Dixon, JE
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (44) : 27445 - 27449
  • [4] Hardy CFJ, 1996, MOL CELL BIOL, V16, P1832
  • [5] Hartwell LH, 1981, MOL BIOL YEAST SACCH, P97
  • [6] PURIFICATION OF HIS-TAGGED PROTEINS IN NONDENATURING CONDITIONS SUGGESTS A CONVENIENT METHOD FOR PROTEIN-INTERACTION STUDIES
    HOFFMANN, A
    ROEDER, RG
    [J]. NUCLEIC ACIDS RESEARCH, 1991, 19 (22) : 6337 - 6338
  • [7] AN ANALYSIS OF 5'-NONCODING SEQUENCES FROM 699 VERTEBRATE MESSENGER-RNAS
    KOZAK, M
    [J]. NUCLEIC ACIDS RESEARCH, 1987, 15 (20) : 8125 - 8148
  • [8] Li DM, 1997, CANCER RES, V57, P2124
  • [9] PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer
    Li, J
    Yen, C
    Liaw, D
    Podsypanina, K
    Bose, S
    Wang, SI
    Puc, J
    Miliaresis, C
    Rodgers, L
    McCombie, R
    Bigner, SH
    Giovanella, BC
    Ittmann, M
    Tycko, B
    Hibshoosh, H
    Wigler, MH
    Parsons, R
    [J]. SCIENCE, 1997, 275 (5308) : 1943 - 1947
  • [10] P-TEN, the tumor suppressor from human chromosome 10q23, is a dual-specificity phosphatase
    Myers, MP
    Stolarov, JP
    Eng, C
    Li, J
    Wang, SI
    Wigler, MH
    Parsons, R
    Tonks, NK
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (17) : 9052 - 9057