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Conformation-dependent phosphorylation of p53
Journal article   Open access   Peer reviewed

Conformation-dependent phosphorylation of p53

Victor Adler, Matthew R. Pincus, Toshinari Minamoto, Serge Y. Fuchs, Mark J. Bluth, Paul W. Brandt-Rauf, Fred K. Friedman, Richard C. Robinson, James M. Chen, Xin Wei Wang, …
Proceedings of the National Academy of Sciences - PNAS, v 94(5), pp 1686-1691
04 Mar 1997
PMID: 9050839
url
http://www.pnas.org/content/94/5/1686.full.pdfView
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Abstract

Biological Sciences
Phosphorylation of the p53 tumor suppressor protein is known to modulate its functions. Using bacterially produced glutathione S -transferase (GST)-p53 fusion protein and baculovirus-expressed histidine-tagged p53 ( His p53), we have determined human p53 phosphorylation by purified forms of jun-N-kinase (JNK), protein kinase A (PKA), and β subunit of casein kinase II (CKIIβ) as well as by kinases present in whole cell extracts (WCEs). We demonstrate that PKA is potent p53 kinase, albeit, in a conformation- and concentration-dependent manner, as concluded by comparing full-length with truncated forms of p53. We further demonstrate JNK interaction with GST-p53 and the ability of JNK to phosphorylate truncated forms of GST-p53 or full-length His p53. Dependence of phosphorylation on conformation of p53 is further supported by the finding that the wild-type form of p53 (p53 wt ) undergoes better phosphorylation by CKIIβ and by WCE kinases than mutant forms of p53 at amino acid 249 (p53 249 ) or 273 (p53 273 ). Moreover, shifting the kinase reaction’s temperature from 37°C to 18°C reduces the phosphorylation of mutant p53 to a greater extent than of p53 wt . Comparing truncated forms of p53 revealed that the ability of CKIIβ, PKA, or WCE kinases to phosphorylate p53 requires amino acids 97–155 within the DNA-binding domain region. Among three 20-aa peptides spanning this region we have identified residues 97–117 that increase p53 phosphorylation by CKIIβ while inhibiting p53 phosphorylation by PKA or WCE kinases. The importance of this region is further supported by computer modeling studies, which demonstrated that mutant p53 249 exhibits significant changes to the conformation of p53 within amino acids 97–117. In summary, phosphorylation-related analysis of different p53 forms in vitro indicates that conformation of p53 is a key determinant in its availability as a substrate for different kinases, as for the phosphorylation pattern generated by the same kinase.

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Web of Science research areas
Biochemistry & Molecular Biology
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