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Mol. Cell. Biol., Jan 1995, 497-504, Vol 15, No. 1
L Wu, JH Bayle, B Elenbaas, NP Pavletich and AJ Levine
The carboxy-terminal domain of the p53 protein comprising amino acid
residues 311 to 393 is able to promote the reassociation of single-
stranded RNA or DNA into duplex hybrids. This domain is as efficient as the
intact p53 protein in both the rate and the extent of the double- stranded
product produced in this reaction. Both wild-type and mutant p53 proteins
from cancerous cells carry out this reaction. The monoclonal antibody
PAb421, which detects an epitope between residues 370 and 378, blocks the
ability of p53 to reassociate single strands of RNA or DNA. Similarly, the
alternative splice form of the murine p53 protein, which removes amino acid
residues 364 to 390 and replaces them with 17 new amino acids, does not
carry out the reassociation reaction with RNA or DNA. This is the first
indication of functionally distinct properties of the alternative splice
forms of p53. These results suggest that this splice alternative can
regulate a p53-mediated reaction that may be related to the functions of
this protein.
Copyright © 1995, American Society for Microbiology
Alternatively spliced forms in the carboxy-terminal domain of the p53 protein regulate its ability to promote annealing of complementary single strands of nucleic acids
Department of Molecular Biology, Princeton University, New Jersey 08544- 1014.
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