Published in

Elsevier, Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, 1-2(600), p. 102-112, 2006

DOI: 10.1016/j.mrfmmm.2006.03.004

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Silent mutations in the gene encoding the p53 protein are preferentially located in conserved amino acid positions and splicing enhancers

Journal article published in 2006 by Guillermo Lamolle, Mónica Marin, Fernando Alvarez-Valin ORCID
This paper is available in a repository.
This paper is available in a repository.

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Abstract

The last release of p53 somatic mutation database contains more than 20,000 of mutation among which 951 are silent (synonymous). This striking amount of silent mutations is much more than what would be expected if synonymous mutations were effectively neutral. The prevalent explanation to reconcile this vast amount of silent mutations with the neutral expectation is that they are just the subproduct of the hypermutability process that affect cancer cells. Some evidences have been presented in this direction, and the explanation has been taken as granted. Assuming that silent mutations are effectively neutral has major implication in the investigation of mutational processes that affect the gene encoding the p53 protein, since on the basis of this assumption they are considered the Null hypothesis, for instance for measuring and comparing among tissues the endogenous mutability. From this it follows that determining whether silent mutations in the p53 gene, and in all disease genes in general, are or not basically mutational noise, is of paramount importance.