Systematic identification of mitotic phosphoproteins

被引:200
作者
Stukenberg, PT
Lustig, KD
McGarry, TJ
King, RW
Kuang, J
Kirschner, MW
机构
[1] HARVARD UNIV,SCH MED,DEPT CELL BIOL,BOSTON,MA 02115
[2] UNIV TEXAS,MD ANDERSON CANCER CTR,DEPT CLIN ONCOL,HOUSTON,TX 77030
关键词
PHASE-SPECIFIC PHOSPHORYLATION; CELL-CYCLE CONTROL; PROTEIN-KINASE; SCHIZOSACCHAROMYCES-POMBE; MONOCLONAL-ANTIBODY; NUCLEAR LAMINA; CDC2; PROTEIN; MITOSIS; ENCODES; INVITRO;
D O I
10.1016/S0960-9822(06)00157-6
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
Background: Cyclin-dependent kinases (CDKs) are thought to initiate and coordinate cell division processes by sequentially phosphorylating key targets; in most cases these substrates remain unidentified. Results: Using a screen that scores for phosphorylation of proteins, which were translated from pools of cDNA plasmids in vitro, by either phosphoepitope antibody recognition or electrophoretic mobility shifts, we have identified 20 mitotically phosphorylated proteins from Xenopus embryos, 15 of which have sequence similarity to other proteins. Of these proteins, five have previously been shown to be phosphorylated during mitosis (epithelial-microtubule associated protein-115, Oct91, Elongation factor 1 gamma, BRG1 and Ribosomal protein L18A), five are related to proteins postulated to have roles in mitosis (epithelial-microtubule associated protein-115, Schizosaccharomyces pombe Cdc5, inner-centrosome protein, BRG1 and the RNA helicase WM6), and nine are related to transcription factors (BRG1, negative co-factor 2 alpha, Oct91, S. pombe Cdc5, HoxD1, Sox3, Vent2, and two isoforms of Xbr1b). Of 16 substrates tested, 14 can be directly phosphorylated in vitro by the mitotic CDK, cyclin B-Cdc2, although three of these may be physiological substrates of other kinases activated during mitosis. Conclusions: Examination of this broad set of mitotic phosphoproteins has allowed us to draw three conclusions about how the activation of CDKs regulates cell-cycle events. First, Cdc2 itself appears to directly phosphorylate most of the mitotic phosphoproteins. Second, during mitosis most of the substrates are phosphorylated more than once and a number may be targets of multiple kinases, suggesting combinatorial regulation. Third, the large fraction of mitotic phosphoproteins that are presumptive transcription factors, two of which have been previously shown to dissociate from DNA during mitosis, suggests that an important function of mitotic phosphorylation is to strip the chromatin of proteins associated with gene expression.
引用
收藏
页码:338 / 348
页数:11
相关论文
共 52 条
  • [1] ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
  • [2] [Anonymous], 1988, Antibodies: a laboratory manual
  • [3] Pombe Cdc5-related protein - A putative human transcription factor implicated in mitogen-activated signaling
    Bernstein, HS
    Coughlin, SR
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (09) : 5833 - 5837
  • [4] CAELLES C, 1995, MOL CELL BIOL, V15, P6694
  • [5] NEGATIVE REGULATION OF THE WEE1 PROTEIN-KINASE BY DIRECT ACTION OF THE NIM1/CDR1 MITOTIC INDUCER
    COLEMAN, TR
    TANG, ZH
    DUNPHY, WG
    [J]. CELL, 1993, 72 (06) : 919 - 929
  • [6] THE INNER CENTROMERE PROTEIN (INCENP) ANTIGENS - MOVEMENT FROM INNER CENTROMERE TO MIDBODY DURING MITOSIS
    COOKE, CA
    HECK, MMS
    EARNSHAW, WC
    [J]. JOURNAL OF CELL BIOLOGY, 1987, 105 (05) : 2053 - 2067
  • [7] DAVIS FM, 1983, P NATL ACAD SCI-BIOL, V80, P2926, DOI 10.1073/pnas.80.10.2926
  • [8] CDC2 PROTEIN-KINASE IS COMPLEXED WITH BOTH CYCLIN-A AND CYCLIN-B - EVIDENCE FOR PROTEOLYTIC INACTIVATION OF MPF
    DRAETTA, G
    LUCA, F
    WESTENDORF, J
    BRIZUELA, L
    RUDERMAN, J
    BEACH, D
    [J]. CELL, 1989, 56 (05) : 829 - 838
  • [9] THE XENOPUS CDC2 PROTEIN IS A COMPONENT OF MPF, A CYTOPLASMIC REGULATOR OF MITOSIS
    DUNPHY, WG
    BRIZUELA, L
    BEACH, D
    NEWPORT, J
    [J]. CELL, 1988, 54 (03) : 423 - 431
  • [10] Faux MC, 1996, TRENDS BIOCHEM SCI, V21, P312, DOI 10.1016/0968-0004(96)10040-2