Cell cycle-regulated expression, phosphorylation, and degradation of p55Cdc - A mammalian homolog of CDC20/Fizzy/slp1

被引:123
作者
Weinstein, J
机构
[1] Amgen Inc., Thousand Oaks
[2] Amgen Inc., Thousand Oaks, CA 91320, 14-1-B
关键词
D O I
10.1074/jbc.272.45.28501
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
p55Cdc is a mammalian protein that shows high homology to the cell cycle proteins Cdc20p of Saccharomyces cerevisiae and the product of the Drosophila fizzy (fly) gene, both of which contain WD repeats and are thought to be required for the metaphase-anaphase transition. The fzy mutants exhibit a metaphase arrest phenotype, which is accompanied by stabilization of cyclins A and B, leading to the hypothesis that fzy function is required for cell cycle-regulated ubiquitin-mediated proteolysis. p55Cdc expression was initiated at the G(1)/S transition and steady state levels of p55Cdc were highest at M and lowest in G(1). Inhibition of the 26 S proteasome prevented both mitotic exit and loss of p55Cdc at the M/G(1) transition, suggesting that p55Cdc degradation was mediated by the cell cycle-regulated proteolytic pathway. Immune complexes of p55Cdc obtained at different cell cycle stages showed a variety of proteins with dramatic differences observed in the pattern of associated proteins during the transition from G(2) to M. Immunolocalization of p55Cdc demonstrated dynamic changes in p55Cdc localization as the cells transit mitosis. p55Cdc appears to act as a regulatory protein interacting with several other proteins, perhaps via its seven WD repeats, at multiple points in the cell cycle.
引用
收藏
页码:28501 / 28511
页数:11
相关论文
共 74 条
[21]   KINETOCHORES, MICROTUBULES AND THE METAPHASE CHECKPOINT [J].
GORBSKY, GJ .
TRENDS IN CELL BIOLOGY, 1995, 5 (04) :143-148
[22]  
Hall LL, 1996, CANCER RES, V56, P3551
[23]   POLO-LIKE KINASE IS A CELL-CYCLE-REGULATED KINASE ACTIVATED DURING MITOSIS [J].
HAMANAKA, R ;
SMITH, MR ;
OCONNOR, PM ;
MALOID, S ;
MIHALIC, K ;
SPIVAK, JL ;
LONGO, DL ;
FERRIS, DK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (36) :21086-21091
[24]   REGULATION OF HUMAN HISTONE GENE-EXPRESSION - KINETICS OF ACCUMULATION AND CHANGES IN THE RATE OF SYNTHESIS AND IN THE HALF-LIVES OF INDIVIDUAL HISTONE MESSENGER-RNAS DURING THE HELA-CELL CYCLE [J].
HEINTZ, N ;
SIVE, HL ;
ROEDER, RG .
MOLECULAR AND CELLULAR BIOLOGY, 1983, 3 (04) :539-550
[25]  
HERSHKO A, 1991, J BIOL CHEM, V266, P16376
[26]   ANAPHASE IS INITIATED BY PROTEOLYSIS RATHER THAN BY THE INACTIVATION OF MATURATION-PROMOTING FACTOR [J].
HOLLOWAY, SL ;
GLOTZER, M ;
KING, RW ;
MURRAY, AW .
CELL, 1993, 73 (07) :1393-1402
[27]   A predictive scale for evaluating cyclin-dependent kinase substrates - A comparison of p34(cdc2) and p33(cdk2) [J].
Holmes, JK ;
Solomon, MJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (41) :25240-25246
[28]   GENES INVOLVED IN SISTER-CHROMATID SEPARATION ARE NEEDED FOR B-TYPE CYCLIN PROTEOLYSIS IN BUDDING YEAST [J].
IRNIGER, S ;
PIATTI, S ;
MICHAELIS, C ;
NASMYTH, K .
CELL, 1995, 81 (02) :269-278
[29]   HUMAN CYCLINS B1 AND B2 ARE LOCALIZED TO STRIKINGLY DIFFERENT STRUCTURES - B1 TO MICROTUBULES, B2 PRIMARILY TO THE GOLGI-APPARATUS [J].
JACKMAN, M ;
FIRTH, M ;
PINES, J .
EMBO JOURNAL, 1995, 14 (08) :1646-1654
[30]  
Kao CT, 1996, ONCOGENE, V13, P1221