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The codon 72 polymorphic variants of p53 have markedly different apoptotic potential.

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TLDR
It is found that in cell lines containing inducible versions of alleles encoding the Pro72 and Arg72 variants, and in cells with endogenous p53, the Arg72 variant induces apoptosis markedly better than does the Pro 72 variant.
Abstract
The gene TP53, encoding p53, has a common sequence polymorphism that results in either proline or arginine at amino-acid position 72. This polymorphism occurs in the proline-rich domain of p53, which is necessary for the protein to fully induce apoptosis. We found that in cell lines containing inducible versions of alleles encoding the Pro72 and Arg72 variants, and in cells with endogenous p53, the Arg72 variant induces apoptosis markedly better than does the Pro72 variant. Our data indicate that at least one source of this enhanced apoptotic potential is the greater ability of the Arg72 variant to localize to the mitochondria; this localization is accompanied by release of cytochrome c into the cytosol. These data indicate that the two polymorphic variants of p53 are functionally distinct, and these differences may influence cancer risk or treatment.

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Citations
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Journal ArticleDOI

Polymorphisms of the Apoptotic genes TP53 and MDM2 and Preeclampsia Development

TL;DR: Despite the clinical features, the distribution of the genotypic variants was similar between case and controls, suggesting that the genetic variants evaluated did not directly influence the risk of PE among the authors' subjects.
Journal ArticleDOI

Association of p53 Codon 72 Polymorphism with Breast Cancer in a Rwandese Population.

TL;DR: The results suggest that p53 codon 72 polymorphism could not be assessed as a risk factor marker for predisposition to breast cancer in Rwanda, and further studies using larger sample sizes are needed to provide more conclusive results.
Journal ArticleDOI

Functional analysis of the p53 codon 72 polymorphism in black South Africans with rheumatoid arthritis--a pilot study.

TL;DR: It is concluded that p53 codon 72 genotype does not influence PL apoptosis or mitochondrial depolarization and is not associated with clinical markers of disease in RA.
Journal ArticleDOI

Association between genetic polymorphisms in apoptosis-related genes and risk of cutaneous melanoma in women and men.

TL;DR: The data suggest for the first time that P53 Arg72Pro, MDM2 c.+309T>G, BAX c.-248G>A, and BCL2 c-717C>A polymorphisms constitute distinct determinants of CM in women and men.
Journal ArticleDOI

Tobacco, Genetic Susceptibility and Lung Cancer

TL;DR: It is hoped that newer research strategies, selecting candidate genes within pathways and genotype at multiple markers within a gene, employing new technologies, may allow complete coverage of the variation within candidate genes in multiple pathways and to unravel the genetic susceptibility to lung cancer.
References
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Journal ArticleDOI

WAF1, a potential mediator of p53 tumor suppression

TL;DR: A gene is identified, named WAF1, whose induction was associated with wild-type but not mutant p53 gene expression in a human brain tumor cell line and that could be an important mediator of p53-dependent tumor growth suppression.
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Mice Lacking p21CIP1/WAF1 undergo normal development, but are defective in G1 checkpoint control

TL;DR: The results establish the role of p21CIP1/WAF1 in the G1 checkpoint, but suggest that the anti-apoptotic and theAnti-oncogenic effects of p53 are more complex.
Journal ArticleDOI

Protein regulation by monoubiquitin

TL;DR: Multi-ubiquitin chains at least four subunits long are required for efficient recognition and degradation of ubiquitylated proteins by the proteasome, but other functions of ubiquitin have been discovered that do not involve the protease.
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Role of a p53 polymorphism in the development of human papillomavirus-associated cancer.

TL;DR: Allelic analysis of patients with HPV-associated tumours revealed a striking overrepresentation of homozygous arginine-72 p53 compared with the normal population, which indicated that individuals homozygously for arginin 72 are about seven times more susceptible to HPV- associated tumorigenesis than heterozygotes.
Journal ArticleDOI

Death signal-induced localization of p53 protein to mitochondria. A potential role in apoptotic signaling

TL;DR: This work proposes a model where p53 can contribute to apoptosis by direct signaling at the mitochondria, thereby amplifying the transcription-dependent apoptosis of p53.
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