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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

A single-nucleotide polymorphism in TP53 may be a genetic risk factor for Iranian patients with idiopathic male infertility

TL;DR: In conclusion, arginine allele appears to be at greater risk of developing idiopathic infertility in Iranian men.
Journal ArticleDOI

p53 codon 72 polymorphism and endometriosis: a meta-analysis

TL;DR: This meta-analysis suggests that p53 codon 72 Pro/Pro + Arg/Pro genotypes are associated with increased risk of endometriosis in Asian, and further studies with larger participants worldwide are needed.
Journal ArticleDOI

Low hMLH1 expression prior to definitive chemoradiotherapy predicts poor prognosis in esophageal squamous cell carcinoma.

TL;DR: It is suggested that the expression of hMLH1 is a potential marker of tumor response and survival and might be useful for selecting esophageal squamous cell carcinoma patients for definitive CCRT.
Journal ArticleDOI

Apaf1 in chronic myelogenous leukemia (CML) progression: reduced Apaf1 expression is correlated with a H179R p53 mutation during clinical blast crisis.

TL;DR: This study has demonstrated mRNA elevation of p53 and apaf1 during CMLblast crisis, indicating that genes and proteins involved in cellular apoptosis might be involved in disease progression/response to therapy.
Journal ArticleDOI

Regulation of p53 expression, phosphorylation and subcellular localization by a G-protein-coupled receptor

TL;DR: The possibility that a GPCR can regulate the apoptotic properties of a chemotherapeutic DNA-damaging agent by regulating the expression, subcellular trafficking and modification of p53 in a manner that is, in part, dependent on the cell type is suggested.
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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