http://www.cnr.it/ontology/cnr/individuo/prodotto/ID11442
Che-1 phosphorylation by ATM/ATR and Chk2 kinases activates p53 transcription and the G2/M checkpoint. (Articolo in rivista)
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- Che-1 phosphorylation by ATM/ATR and Chk2 kinases activates p53 transcription and the G2/M checkpoint. (Articolo in rivista) (literal)
- Anno
- 2006-01-01T00:00:00+01:00 (literal)
- Alternative label
Bruno T.; De Nicola F.; Iezzi S. Lecis D.; D'Angelo C.; Di Padova M.; Corbi N.; Zannini L.; Jekimovs C.; Scarsella M.; Porrello A.; Crescenzi M.; Leonetti C.; Khanna K.K.; Soddu S.; Floridi A.; Passananti C .; Delia D.; Fanciulli, M. (2006)
Che-1 phosphorylation by ATM/ATR and Chk2 kinases activates p53 transcription and the G2/M checkpoint.
in Cancer cell (Print)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Bruno T.; De Nicola F.; Iezzi S. Lecis D.; D'Angelo C.; Di Padova M.; Corbi N.; Zannini L.; Jekimovs C.; Scarsella M.; Porrello A.; Crescenzi M.; Leonetti C.; Khanna K.K.; Soddu S.; Floridi A.; Passananti C .; Delia D.; Fanciulli, M. (literal)
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- ISI Web of Science (WOS) (literal)
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- Experimental Chemotherapy Laboratory, Department of Experimental Oncology, Regina Elena Cancer Institute, 00158 Rome, Italy;
Laboratory B, Department of Therapeutic Programs Development, Regina Elena Cancer Institute, 00158 Rome, Italy;
Department of Experimental Medicine, University of L'Aquila, 67100 L'Aquila, Italy;
Department of Experimental Oncology, Istituto Nazionale Tumori, 20133 Milan, Italy;
Istituto di Biologia e Patologia Molecolare, CNR, 00158 Rome, Italy;
Department of Environment and Primary Prevention, High Institute of Health, 00161 Rome, Italy;
Queensland Institute of Medical Research, P.O. Royal Brisbane Hospital, Brisbane, Queensland 4029, Australia;
8Molecular Oncogenesis Laboratory, Department of Experimental Oncology, Regina Elena Cancer Institute, 00158 Rome, Italy
9Laboratory D, Department of Therapeutic Programs Development, Regina Elena Cancer (literal)
- Titolo
- Che-1 phosphorylation by ATM/ATR and Chk2 kinases activates p53 transcription and the G2/M checkpoint. (literal)
- Abstract
- Che-1 is a RNA polymerase II-binding protein involved in the transcription of E2F target genes and induction of cell proliferation.
Here we show that Che-1 contributes to DNA damage response and that its depletion sensitizes cells to anticancer
agents. The checkpoint kinases ATM/ATR and Chk2 interact with Che-1 and promote its phosphorylation and accumulation
in response to DNA damage. These Che-1 modifications induce a specific recruitment of Che-1 on the TP53 and p21 promoters.
Interestingly, it has a profound effect on the basal expression of p53, which is preserved following DNA damage.
Notably, Che-1 contributes to the maintenance of the G2/M checkpoint induced by DNA damage. These findings identify
a mechanism by which checkpoint kinases regulate responses to DNA damage. (literal)
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