Multiple Cdk1 inhibitory kinases regulate the cell cycle during development

被引:35
作者
Leise, WF
Mueller, PR
机构
[1] Univ Chicago, Dept Mol Genet & Cell Biol, Ctr Mol Oncol, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Biochem & Mol Biol, Chicago, IL 60637 USA
[3] Univ Chicago, Comm Dev Biol, Chicago, IL 60637 USA
[4] Univ Chicago, Comm Canc Biol, Chicago, IL 60637 USA
[5] Univ Chicago, Comm Genet, Chicago, IL 60637 USA
关键词
Wee1; Myt1; Wee2; Cdc2; gastrulation; cell cycle; Xenopus; cell division; morphogenesis; embryogenesis;
D O I
10.1006/dbio.2002.0743
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Wee kinases block entry into mitosis by phosphorylating and inhibiting the activity of the mitotic cyclin-dependent kinase, Cdk1. We have found that the various Xenopus Wee kinases have unique temporal and spatial patterns of expression during development. In addition, we have isolated and characterized a new Wee1-like kinase, Xenopus Wee2. By both in vivo and in vitro tests, Xenopus Wee2 functions as a Wee1-like kinase. The previously isolated Wee1-like kinase, Xenopus Wee1, is expressed only as maternal gene product. In contrast, Xenopus Wee2 is predominantly a zygotic gene product, while the third Wee kinase, Xenopus Myt1, is both a maternal and zygotic gene product. Concurrent with the changing levels of these Cdk inhibitory kinases, the pattern of embryonic cell division becomes asynchronous and spatially restricted in the Xenopus embryo. Interestingly, once zygotic transcription begins, Xenopus Wee2 is expressed in regions of the embryo that are devoid of mitotic cells, such as the involuting mesoderm. In contrast, Xenopus Myt1 is expressed in regions of the embryo that have high levels of proliferation, such as the developing neural tissues. The existence of multiple Wee kinases may help explain how distinct patterns of cell division arise and are regulated during development. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:156 / 173
页数:18
相关论文
共 72 条
[41]   Cell cycle transition in early embryonic development of Xenopus laevis [J].
Masui, Y ;
Wang, P .
BIOLOGY OF THE CELL, 1998, 90 (08) :537-548
[42]   Tribbles coordinates mitosis and morphogenesis in Drosophila by regulating string/CDC25 proteolysis [J].
Mata, J ;
Curado, S ;
Ephrussi, A ;
Rorth, P .
CELL, 2000, 101 (05) :511-522
[43]   THIAMINE-REPRESSIBLE EXPRESSION VECTORS PREP AND PRIP FOR FISSION YEAST [J].
MAUNDRELL, K .
GENE, 1993, 123 (01) :127-130
[44]  
MORENO S, 1991, METHOD ENZYMOL, V194, P795
[45]   Cyclin-dependent kinases: Engines, clocks, and microprocessors [J].
Morgan, DO .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1997, 13 :261-291
[46]   CONSTITUTIVE AND METAL-INDUCIBLE PROTEIN - DNA INTERACTIONS AT THE MOUSE METALLOTHIONEIN-I PROMOTER EXAMINED BY INVIVO AND INVITRO FOOTPRINTING [J].
MUELLER, PR ;
SALSER, SJ ;
WOLD, B .
GENES & DEVELOPMENT, 1988, 2 (04) :412-427
[47]   CELL-CYCLE REGULATION OF A XENOPUS WEE1-LIKE KINASE [J].
MUELLER, PR ;
COLEMAN, TR ;
DUNPHY, WG .
MOLECULAR BIOLOGY OF THE CELL, 1995, 6 (01) :119-134
[48]   MYT1 - A MEMBRANE-ASSOCIATED INHIBITORY KINASE THAT PHOSPHORYLATES CDC2 ON BOTH THREONINE-14 AND TYROSINE-15 [J].
MUELLER, PR ;
COLEMAN, TR ;
KUMAGAI, A ;
DUNPHY, WG .
SCIENCE, 1995, 270 (5233) :86-90
[49]   Mos positively regulates Xe-Wee1 to lengthen the first mitotic cell cycle of Xenopus [J].
Murakami, MS ;
Copeland, TD ;
Vande Woude, GF .
GENES & DEVELOPMENT, 1999, 13 (05) :620-631
[50]  
Murakami MS, 1998, DEVELOPMENT, V125, P237