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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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Interleukin-1β causes excitotoxic neurodegeneration and multiple sclerosis disease progression by activating the apoptotic protein p53

TL;DR: The role of the apoptotic cascade in the synaptic abnormalities and neuronal loss caused by the proinflammatory cytokines interleukin-1β and tumor necrosis factor in brain tissues, and disease progression caused by inflammation in relapsing-remitting MS patients, is addressed.
Journal ArticleDOI

p53: at the crossroad between cancer and ageing.

TL;DR: A number of models with altered p53 function are presented and it is discussed how these models implicate p53 as part of a molecular network that integrates tumour suppression and ageing.
Journal ArticleDOI

p53: a heavily dictated dictator of life and death

TL;DR: The majority of the progress made during the past two years has focused on the cellular factors and post-translational modifications that regulate the expression levels and activities of p53 in response to stress signals.
Journal ArticleDOI

TP53 is frequently altered by methylation, mutation, and/or deletion in acute lymphoblastic leukaemia.

TL;DR: This study has analysed the complete coding region, all intron‐exon junctions and noncoding regions of exons 1–11 of TP53 by lexon‐DGGE, and found promoter methylation in 32% of the cases, missense mutations in 8.8%, and deletion of one allele in 7.5%, with TP53 being altered in 40% of all the ALL samples studied in this series.
Journal ArticleDOI

Post-Traumatic Brain Injury: Genetic Susceptibility to Outcome

TL;DR: It is evident that contradicting results are attributable to the heterogeneity of studies, thus further researches are warranted to effectively assess a relation between genetic traits and clinical outcome following traumatic injuries.
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.
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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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