TP53 tumor suppressor gene: A model for investigating human mutagenesis
- 1 January 1992
- journal article
- review article
- Published by Wiley in Genes, Chromosomes and Cancer
- Vol. 4 (1), 1-15
- https://doi.org/10.1002/gcc.2870040102
Abstract
More than 350 independent point mutations of the TP53 gene, found in a wide variety of human cancers, were compiled and analysed. From this study, we confirm the presence of four hot‐spot regions which colocalize with some highly conserved domains of the protein. We also define a new hot‐spot region which is observed predominantly in lung tumors. Analysis of the mutational events suggests the direct involvement of environmental carcinogens in lung tumors and hepatocarcinomas, and spontaneous mutagenesis generating essentially CpG transitions in most of the remaining ones. Furthermore, we demonstrate in this work that the TP53 gene is an informative model with which to study the molecular mechanisms of mutagenesis in the human genome.Keywords
This publication has 54 references indexed in Scilit:
- The p53 tumour suppressor geneNature, 1991
- The spectrum of molecular alterations in the evolution of chronic myelocytic leukemia.Journal of Clinical Investigation, 1991
- Point mutation of the p53 gene resulting in splicing inhibition in small cell lung carcinomaBiochemical and Biophysical Research Communications, 1990
- 5-Methylcytosine as an Endogenous Mutagen in the Human LDL Receptor and p53 GenesScience, 1990
- A splicing mutation accounts for the lack of p53 gene expression in a CML blast crisis cell line: a novel mechanism of p53 gene inactivationBritish Journal of Haematology, 1990
- Identification of intronic point mutations as an alternative mechanism for p53 inactivation in lung cancer.Journal of Clinical Investigation, 1990
- Frequency of abnormal human haemoglobins caused by C → T transitions in CpG dinucleotidesJournal of Molecular Biology, 1990
- Mutations in the p53 gene occur in diverse human tumour typesNature, 1989
- Chromosome 17 Deletions and p53 Gene Mutations in Colorectal CarcinomasScience, 1989
- Molecular basis of base substitution hotspots in Escherichia coliNature, 1978