Document Detail


ADP-ribosylation of p53 tumor suppressor protein: mutant but not wild-type p53 is modified.
MedLine Citation:
PMID:  8836878     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Poly(ADP-ribosyl)ation of mutant and wild-type p53 was studied in transformed and nontransformed rat cell lines constitutively expressing the temperature-sensitive p53135val. It was found that in both cell types at 37.5 degrees C, where overexpressed p53 exhibits mutant conformation and cytoplasmic localization, a considerable part of the protein was poly(ADP-ribosyl)ated. Using densitometric scanning, the molecular mass of the modified protein was estimated as 64 kD. Immunofluorescence studies with affinity purified anti-poly(ADP-ribose) transferase (pADPRT) antibodies revealed that, contrary to predictions, the active enzyme was located in the cytoplasm, while in nuclei chromatin was depleted of pADPRT. A distinct intracellular localization and action of pADPRT was found in the cell lines cultivated at 32.5 degrees C, where p53 adopts wild-type form. Despite nuclear coexistence of both proteins no significant modification of p53 was found. Since the strikingly shared compartmentalization of p53 and pADPRT was indicative of possible complex formation between the two proteins, reciprocal immunoprecipitation and immunoblotting were performed with anti-p53 and anti-pADPRT antibodies. A poly(ADP-ribosyl)ated protein of 116 kD constantly precipitated at stringent conditions was identified as the automodified enzyme. It is concluded that mutant cytoplasmic p53 is tightly complexed to pADPRT and becomes modified. At 32.5 degrees C binding to DNA of p53 or its temperature-dependent conformational alteration might prevent an analogous modification of the tumor suppressor protein.
Authors:
J Wesierska-Gadek; A Bugajska-Schretter; C Cerni
Related Documents :
16135518 - Nucleo-cytoplasmic shuttling of high risk human papillomavirus e2 proteins induces apop...
7954368 - P53 proteins accumulated by heat stress associate with heat shock proteins hsp72/hsc73 ...
14757278 - Expression of p53 family in scars.
7508568 - Influence of the processing of muca protein on the reversion of the frameshift hisd3052...
667008 - Molecular weight in detergent solution of acetylcholine receptor from torpedo californica.
17572408 - Identification and characterization of two novel (neuro)endocrine long coiled-coil prot...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Journal of cellular biochemistry     Volume:  62     ISSN:  0730-2312     ISO Abbreviation:  J. Cell. Biochem.     Publication Date:  1996 Jul 
Date Detail:
Created Date:  1996-12-11     Completed Date:  1996-12-11     Revised Date:  2008-11-21    
Medline Journal Info:
Nlm Unique ID:  8205768     Medline TA:  J Cell Biochem     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  90-101     Citation Subset:  IM    
Affiliation:
Institute of Tumorbiology-Cancer Research, University of Vienna, Austria.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adenosine Diphosphate Ribose / metabolism*
Animals
Cell Division / genetics
Cell Line
Cell Transformation, Neoplastic / genetics
Hot Temperature
Mutation
Phenotype
Rats
Rats, Inbred F344
Tumor Suppressor Protein p53 / genetics,  metabolism*
Chemical
Reg. No./Substance:
0/Tumor Suppressor Protein p53; 20762-30-5/Adenosine Diphosphate Ribose

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Protein kinase C activation inhibits stress-induced synthesis of heat shock protein 27 in osteoblast...
Next Document:  NDF induces expression of a novel 46 kD protein in estrogen receptor positive breast cancer cells.