SUBSTRATE-SPECIFICITY AND CELL-CYCLE REGULATION OF THE NEK2 PROTEIN-KINASE, A POTENTIAL HUMAN HOMOLOG OF THE MITOTIC REGULATOR NIMA OF ASPERGILLUS-NIDULANS

被引:133
作者
FRY, AM
SCHULTZ, SJ
BARTEK, J
NIGG, EA
机构
[1] SWISS INST EXPTL CANC RES, CH-1066 EPALINGES, SWITZERLAND
[2] DANISH CANC SOC, DIV CANC BIOL, DK-2100 COPENHAGEN, DENMARK
关键词
D O I
10.1074/jbc.270.21.12899
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
The human Nek2 protein kinase is the closest known mammalian relative of the mitotic regulator NIMA of Aspergillus nidulans, The two kinases share 47% sequence identity over their catalytic domains and display a similar cell cycle-dependent expression peaking at the G(2) to M phase transition. Hence, it is attractive to speculate that human Nek2 and fungal NIMA may carry out similar functions at the onset of mitosis, To study the biochemical properties and substrate specificity of human Nek2 and compare them to those reported previously for other NIMA-related protein kinases, we have expressed Nek2 in insect cells. We show that recombinant Nek2 is active as a serine/threonine-specific protein kinase and may undergo autophosphorylation. Both human Nek2 and fungal NIMA phosphorylate a similar, albeit not identical, set of proteins and synthetic peptides, and beta-casein was found to be a suitable substrate for assaying Nek2 in vitro. By exploiting these findings, we have studied the cell cycle regulation of Nek2 activity in HeLa cells. We show that Nek2 activity parallels its abundance, being low during M and G(1) but high during S and G(2) phase. Taken together, our results suggest that human Nek2 resembles fungal NIMA in its primary structure, cell cycle regulation of expression, and substrate specificity, but that Nek2 may function earlier in the cell cycle than NIMA.
引用
收藏
页码:12899 / 12905
页数:7
相关论文
共 27 条
[1]   A MAMMALIAN PROTEIN-KINASE WITH POTENTIAL FOR SERIN THREONINE AND TYROSINE PHOSPHORYLATION IS RELATED TO CELL-CYCLE REGULATORS [J].
BENDAVID, Y ;
LETWIN, K ;
TANNOCK, L ;
BERNSTEIN, A ;
PAWSON, T .
EMBO JOURNAL, 1991, 10 (02) :317-325
[2]   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
[3]   PHOSPHOTRANSFERASE AND SUBSTRATE BINDING MECHANISM OF THE CAMP-DEPENDENT PROTEIN-KINASE CATALYTIC SUBUNIT FROM PORCINE HEART AS DEDUCED FROM THE 2.0 ANGSTROM STRUCTURE OF THE COMPLEX WITH MN2+ ADENYLYL IMIDODIPHOSPHATE AND INHIBITOR PEPTIDE PKI(5-24) [J].
BOSSEMEYER, D ;
ENGH, RA ;
KINZEL, V ;
PONSTINGL, H ;
HUBER, R .
EMBO JOURNAL, 1993, 12 (03) :849-859
[4]  
DOONAN JH, 1992, J CELL SCI, V103, P599
[5]  
HANKS SK, 1991, METHOD ENZYMOL, V200, P38
[6]  
HARLOW E, 1988, ANTIBODIES LABORATOR
[7]   PROTEIN-TYROSINE KINASES [J].
HUNTER, T ;
COOPER, JA .
ANNUAL REVIEW OF BIOCHEMISTRY, 1985, 54 :897-930
[8]  
KEMP BE, 1977, J BIOL CHEM, V252, P4888
[9]   STRUCTURE OF A PEPTIDE INHIBITOR BOUND TO THE CATALYTIC SUBUNIT OF CYCLIC ADENOSINE-MONOPHOSPHATE DEPENDENT PROTEIN-KINASE [J].
KNIGHTON, DR ;
ZHENG, JH ;
TENEYCK, LF ;
XUONG, NH ;
TAYLOR, SS ;
SOWADSKI, JM .
SCIENCE, 1991, 253 (5018) :414-420
[10]  
KUENZEL EA, 1987, J BIOL CHEM, V262, P9136