Abstract
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 temperature-sensitive (ts) cdc25ts mutant that is unable to initiate mitosis. In HeLa 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.
MeSH Terms
Amino Acid Sequence
Base Sequence
Cloning, Molecular/methods
Gene Expression
Gene Library
HeLa Cells/cytology
Humans
Interphase
Kinetics
Molecular Sequence Data
Mutation
Oligonucleotide Probes
Proteins/genetics
RNA, Messenger/genetics
Schizosaccharomyces/genetics
Sequence Homology, Nucleic Acid
cdc25 Phosphatases
Chemicals
Oligonucleotide Probes
Proteins
RNA, Messenger
cdc25 Phosphatases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Sadhu K
Department of Molecular Biology, Research Institute of Scripps Clinic, La Jolla, CA 92037.
Reed S I
Richardson H
Russell P
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