http://www.cnr.it/ontology/cnr/individuo/prodotto/ID283031
CK1delta Kinase Activity Is Modulated by Chk1-Mediated Phosphorylation (Articolo in rivista)
- Type
- Label
- CK1delta Kinase Activity Is Modulated by Chk1-Mediated Phosphorylation (Articolo in rivista) (literal)
- Anno
- 2013-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1371/journal.pone.0068803 (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Bischof J.; Randoll S.-J.; Sussner N.; Henne-Bruns D.; Pinna L.A.; Knippschild U. (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
- http://www.scopus.com/inward/record.url?eid=2-s2.0-84879803037&partnerID=q2rCbXpz (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
- Note
- Scopu (literal)
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Department of General and Visceral Surgery, Ulm University Hospital, Ulm, Germany; Department of Biological Sciences and Consiglio Nazionale delle Ricerche Neuroscience Institute, University of Padova, Padova, Italy (literal)
- Titolo
- CK1delta Kinase Activity Is Modulated by Chk1-Mediated Phosphorylation (literal)
- Abstract
- CK1?, a member of the casein kinase 1 family, is involved in the regulation of various cellular processes and has been associated with the pathophysiology of neurodegenerative diseases and cancer. Therefore recently, interest in generating highly specific inhibitors for personalized therapy has increased enormously. However, the efficacy of newly developed inhibitors is affected by the phosphorylation state of CK1?. Cellular kinases phosphorylating CK1? within its C-terminal domain have been identified but still more information regarding the role of site-specific phosphorylation in modulating the activity of CK1? is required. Here we show that Chk1 phosphorylates rat CK1? at serine residues 328, 331, 370, and threonine residue 397 as well as the human CK1? transcription variants 1 and 2. CK1? mutant proteins bearing one, two or three mutations at these identified phosphorylation sites exhibited significant differences in their kinetic properties compared to wild-type CK1?. Additionally, CK1? co-precipitates with Chk1 from HT1080 cell extracts and activation of cellular Chk1 resulted in a significant decrease in cellular CK1? kinase activity. Taken together, these data point towards a possible regulatory relationship between Chk1 and CK1?. © 2013 Bischof et al. (literal)
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