Cell cycle regulation in Aspergillus by two protein kinases

被引:75
作者
Osmani, SA
Ye, XS
机构
[1] Weis Center for Research, Geisinger Clinic, Danville
关键词
D O I
10.1042/bj3170633
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
Great progress has recently been made in our understanding of the regulation of the eukaryotic cell cycle, and the central role of cyclin-dependent kinases is now clear. In Aspergillus nidulans it has been established that a second class of cell-cycle-regulated protein kinases, typified by NIMA. (encoded by the nimA gene), is also required for cell cycle progression into mitosis. Indeed, both p34(cdc)2/cyclin B and NIMA have to be correctly activated before mitosis can be initiated in this species, and p34(cdc2)/cyclin B plays a role in the mitosis-specific activation of NIMA. In addition, both kinases have to be proteolytically destroyed before mitosis can be completed. NIMA-related kinases may also regulate the cell cycle in other eukaryotes, as expression of MMA can promote mitotic events in yeast, frog or human cells. Moreover, dominant-negative versions of NIMA can adversely affect the progression of human cells into mitosis, as they do in A. nidulans. The ability of NIMA to influence mitotic regulation in human and frog cells strongly suggests the existence of a NIMA pathway of mitotic regulation in higher eukaryotes. A growing number of NIMA-related kinases have been isolated from organisms ranging from fungi to humans, and some of these kinases are also cell-cycle-regulated. How NIMA-related kinases and cyclin-dependent kinases act in concert to promote cell cycle transitions is just beginning to be understood. This understanding is the key to a full knowledge of cell cycle regulation.
引用
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页码:633 / 641
页数:9
相关论文
共 127 条
[1]   DISTINCT NUCLEAR AND SPINDLE POLE BODY POPULATIONS OF CYCLIN-CDC2 IN FISSION YEAST [J].
ALFA, CE ;
DUCOMMUN, B ;
BEACH, D ;
HYAMS, JS .
NATURE, 1990, 347 (6294) :680-682
[2]   REGULATION OF P34CDC28 TYROSINE PHOSPHORYLATION IS NOT REQUIRED FOR ENTRY INTO MITOSIS IN SACCHAROMYCES-CEREVISIAE [J].
AMON, A ;
SURANA, U ;
MUROFF, I ;
NASMYTH, K .
NATURE, 1992, 355 (6358) :368-371
[3]   CLOSING THE CELL-CYCLE CIRCLE IN YEAST - G2 CYCLIN PROTEOLYSIS INITIATED AT MITOSIS PERSISTS UNTIL THE ACTIVATION OF G1 CYCLINS IN THE NEXT CYCLE [J].
AMON, A ;
IRNIGER, S ;
NASMYTH, K .
CELL, 1994, 77 (07) :1037-1050
[4]   CLONING OF CHROMOSOME-I DNA FROM SACCHAROMYCES-CEREVISIAE - ANALYSIS OF THE FUN52-GENE, WHOSE PRODUCT HAS HOMOLOGY TO PROTEIN-KINASES [J].
BARTON, AB ;
DAVIES, CJ ;
HUTCHISON, CA ;
KABACK, DB .
GENE, 1992, 117 (01) :137-140
[5]  
BEACH D, 1982, NATURE, V300, P705
[6]   S-PHASE, G2, AND NUCLEAR DIVISION MUTANTS OF ASPERGILLUS-NIDULANS [J].
BERGEN, LG ;
UPSHALL, A ;
MORRIS, NR .
JOURNAL OF BACTERIOLOGY, 1984, 159 (01) :114-119
[7]   THE FISSION YEAST CDC2 CDC13 SUC1 PROTEIN-KINASE - REGULATION OF CATALYTIC ACTIVITY AND NUCLEAR-LOCALIZATION [J].
BOOHER, RN ;
ALFA, CE ;
HYAMS, JS ;
BEACH, DH .
CELL, 1989, 58 (03) :485-497
[8]   CDC7 PROTEIN-KINASE ACTIVITY IS REQUIRED FOR MITOSIS AND MEIOSIS IN SACCHAROMYCES-CEREVISIAE [J].
BUCK, V ;
WHITE, A ;
ROSAMOND, J .
MOLECULAR & GENERAL GENETICS, 1991, 227 (03) :452-457
[9]   ALPHA-HELICAL COILED COILS - A WIDESPREAD MOTIF IN PROTEINS [J].
COHEN, C ;
PARRY, DAD .
TRENDS IN BIOCHEMICAL SCIENCES, 1986, 11 (06) :245-248
[10]  
DAVIS FM, 1983, P NATL ACAD SCI-BIOL, V80, P2926, DOI 10.1073/pnas.80.10.2926