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Target Concepts:
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Query: EC:2.7.11.22 (
cdc2
)
8,319
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
CDC6
is conserved during evolution and is essential and limiting for the initiation of eukaryotic DNA replication. Human
CDC6
activity is regulated by periodic transcription and
CDK
-regulated subcellular localization. Here, we show that, in addition to being absent from nonproliferating cells,
CDC6
is targeted for ubiquitin-mediated proteolysis by the anaphase promoting complex (APC)/cyclosome in G(1). A combination of point mutations in the destruction box and KEN-box motifs in
CDC6
stabilizes the protein in G(1) and in quiescent cells. Furthermore, APC, in association with CDH1, ubiquitinates
CDC6
in vitro, and both APC and CDH1 are required and limiting for
CDC6
proteolysis in vivo. Although a stable mutant of
CDC6
is biologically active, overexpression of this mutant or wild-type
CDC6
is not sufficient to induce multiple rounds of DNA replication in the same cell cycle. The APC-CDH1-dependent proteolysis of
CDC6
in early G(1) and in quiescent cells suggests that this process is part of a mechanism that ensures the timely licensing of replication origins during G(1).
...
PMID:Cell cycle- and cell growth-regulated proteolysis of mammalian CDC6 is dependent on APC-CDH1. 1099 89
In eukaryotic cells, the function of DNA replication licensing components (Cdc6 and Cdt1, among others) is crucial for cell proliferation and genome stability. However, little is known about their role in whole organisms and whether licensing control interfaces with differentiation and developmental programs. Here, we study Arabidopsis thaliana CDT1, its regulation, and the consequences of overriding licensing control. The availability of AtCDT1 is strictly regulated at two levels: (1) at the transcription level, by E2F and growth-arresting signals, and (2) posttranscriptionally, by
CDK
phosphorylation, a step that is required for its proteasome-mediated degradation. We also show that
CDC6
and CDT1 are key targets for the coordination of cell proliferation, differentiation, and development. Indeed, altered CDT1 or
CDC6
levels have cell type-specific effects in developing Arabidopsis plants: in leaf cells competent to divide, cell proliferation is stimulated, whereas in cells programmed to undergo differentiation-associated endoreplication rounds, extra endocycles are triggered. Thus, we propose that DNA replication licensing control is critical for the proper maintenance of proliferative potential, developmental programs, and morphogenetic patterns.
...
PMID:DNA replication licensing affects cell proliferation or endoreplication in a cell type-specific manner. 1531 10
Fertilization relieves the oocyte from a cell cycle arrest, inducing progression towards mitotic cycles. While the signalling pathways involved in oocyte to embryo transition have been widely investigated, how they specifically trigger DNA replication is still unclear. We used sea urchin eggs whose oocytes are arrested in G1 to investigate in vivo the molecular mechanisms regulating initiation of replication after fertilization. Unexpectedly, we found that
CDC6
, Cdt1 and MCM3, components of the pre-replication complexes (pre-RC) which license origins for replication, were already loaded on female chromatin before fertilization. This is the first demonstration of a cell cycle arrest in metazoan in which chromatin is already licensed for replication. In contrast pre-RC assemble on chromatin post-fertilization as in other organisms. These differences in the timing of pre-RC assembly are accompanied by differences in
Cdk2
requirement for DNA replication initiation between female and male chromatin post-fertilization. Finally, we demonstrated that a concomitant inhibition of MAP kinase and ATM/ATR pathways releases the block to DNA synthesis. Our findings provide new insight into the mechanisms contributing to the release of G1 arrest and the control of S-phase entry at fertilization.
...
PMID:Replication origins are already licensed in G1 arrested unfertilized sea urchin eggs. 2015 11