REGULATION OF THE G2-MITOSIS TRANSITION

被引:21
作者
FEILOTTER, H
LINGNER, C
ROWLEY, R
YOUNG, PG
机构
[1] QUEENS UNIV, DEPT BIOL, KINGSTON K7L 3N6, ONTARIO, CANADA
[2] COLD SPRING HARBOR LAB, COLD SPRING HARBOR, NY 11724 USA
[3] UNIV UTAH, DEPT RADIOL, SALT LAKE CITY, UT 84132 USA
关键词
CELL CYCLE; MITOSIS; SCHIZOSACCHAROMYCES-POMBE; CDC2; P34;
D O I
10.1139/o92-140
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 cell cycle is regulated by pathways composed of a dependent series of steps, by timers, and by checkpoint controls which ensure the completion of one event before the initiation of another. This review focusses on the regulation of the initiation of mitosis, with particular emphasis on the regulation of p34cdc2 activity at this point in the cell cycle. The review draws on data from various organisms, but strongly emphasizes the genetic framework as seen in the fission yeast Schizosaccharomyces pombe and the biology and biochemistry of maturation promoting factor in frog oocytes. An attempt is made to include all known genes and proteins where a link can be made to the initiation event. The nutritional size control and its major known controlling elements, the wee1/mik1 protein kinases, and cdc25 protein tyrosine phosphatase are considered in detail along with their regulation. In addition, the checkpoint control pathways which mediate G2 delay in response to failure of DNA replication or DNA damage are examined.
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页码:954 / 971
页数:18
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