HUMAN HOMOLOG OF FISSION YEAST CDC25 MITOTIC INDUCER IS PREDOMINANTLY EXPRESSED IN G2

被引:327
|
作者
SADHU, K [1 ]
REED, SI [1 ]
RICHARDSON, H [1 ]
RUSSELL, P [1 ]
机构
[1] SCRIPPS CLIN & RES FDN,RES INST,DEPT MOLEC BIOL,10666 N TORREY PINES RD,LA JOLLA,CA 92037
关键词
Cell cycle; HeLa; Mitosis; Mitotic control;
D O I
10.1073/pnas.87.13.5139
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Entry into mitosis during the somatic cell cycle is regulated in response to signals that monitor the completion of DNA replication, the integrity of the nuclear genome, and, possibly, the increase in cellular mass during the cell cycle. It has been postulated that the operation of this cell cycle control involves the gradual accumulation of rate-limiting mitotic inducers, which trigger nuclear division when their cellular concentration reaches a critical level. We have cloned a human gene, which we call CDC25, whose product may function as a mitotic inducer. This human gene encodes a protein with a predicted molecular mass of 53,000 daltons whose C-terminal domain shares about 37% sequence identity with the fission yeast cdc25+ mitotic inducer. The human CDC25 gene rescues the defect of a fission yeast temperaturesensitive (ts) cdc25ts mutant that is unable to initiate mitosis. In HcLa cells CDC25 mRNA levels are very low in G1 and increase at least 4-fold as cells progress towards M phase. These data suggest that in human cells, as in fission yeast, the accumulation of CDC25 mitotic inducer during G2 may play a key role in regulating the timing of mitosis.
引用
收藏
页码:5139 / 5143
页数:5
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