Collaborative role of E2F transcriptional activity and G1 cyclin-dependent kinase activity in the induction of S phase
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Leone, G
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Duke Univ, Med Ctr, Howard Hughes Med Inst, Dept Genet, Durham, NC 27710 USADuke Univ, Med Ctr, Howard Hughes Med Inst, Dept Genet, Durham, NC 27710 USA
Leone, G
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DeGregori, J
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Duke Univ, Med Ctr, Howard Hughes Med Inst, Dept Genet, Durham, NC 27710 USADuke Univ, Med Ctr, Howard Hughes Med Inst, Dept Genet, Durham, NC 27710 USA
DeGregori, J
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Jakoi, L
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Duke Univ, Med Ctr, Howard Hughes Med Inst, Dept Genet, Durham, NC 27710 USADuke Univ, Med Ctr, Howard Hughes Med Inst, Dept Genet, Durham, NC 27710 USA
Jakoi, L
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Cook, JG
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Duke Univ, Med Ctr, Howard Hughes Med Inst, Dept Genet, Durham, NC 27710 USADuke Univ, Med Ctr, Howard Hughes Med Inst, Dept Genet, Durham, NC 27710 USA
Cook, JG
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Nevins, JR
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Duke Univ, Med Ctr, Howard Hughes Med Inst, Dept Genet, Durham, NC 27710 USADuke Univ, Med Ctr, Howard Hughes Med Inst, Dept Genet, Durham, NC 27710 USA
Nevins, JR
[1
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[1] Duke Univ, Med Ctr, Howard Hughes Med Inst, Dept Genet, Durham, NC 27710 USA
A considerable body of evidence points to a role for both cyclin E/cyclin-dependent kinase (cdk)2 activity and E2F transcription activity in the induction of S phase. We show that overexpression of cyclin E/cdk2 in quiescent cells induces S phase, that this coincides with an induction of E2F activity, and that coexpression of E2F enhances the cyclin E/cdk2 mediated induction of S phase. Likewise, E2F overexpression can induce S phase and does so in the apparent absence of cyclin E/cdk2 activity. In addition, although the inhibition of cyclin E/cdk2 activity blocks the induction of S phase after growth stimulation of normal mouse embryo fibroblasts, inhibition of cyclin E/cdk2 does not block S phase induction in Rb-/- cells where E2F activity is deregulated. These results point to the important roles for E2F and cyclin E/cdk2 in the induction of S phase. Moreover, the nature of the E2F targets and the suspected targets for cyclin E/cdk2 suggests a potential molecular mechanism for the collaborative action of cyclin E/cdk2 and E2F in the induction of S phase.