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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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Puma is an essential mediator of p53-dependent and -independent apoptotic pathways

TL;DR: It is reported that Puma is essential for hematopoietic cell death triggered by ionizing radiation, deregulated c-Myc expression, and cytokine withdrawal, and required for IR-induced death throughout the developing nervous system and accounts for nearly all of the apoptotic activity attributed to p53 under these conditions.
Journal ArticleDOI

TP53 mutations in human cancers: functional selection and impact on cancer prognosis and outcomes

TL;DR: It is shown that intrinsic mutagenicity rates, loss of transactivation activities, and to a lesser extent, dominant-negative activities are the main driving forces that determine TP53 mutation patterns and influence tumor phenotype.
Journal ArticleDOI

Mitochondrial p53 activates Bak and causes disruption of a Bak-Mcl1 complex

TL;DR: It is shown that, after cell stress, p53 interacts with the pro-apoptotic mitochondrial membrane protein Bak, which is consistent with a model in which p53 and Mcl1 have opposing effects on mitochondrial apoptosis by interacting with, and modulating the activity of, the death effector Bak.
Journal ArticleDOI

The P53 pathway: what questions remain to be explored?

TL;DR: The p53 pathway is composed of hundreds of genes and their products that respond to a wide variety of stress signals that play a role in protection from cancers, therapy and integrating the homeostatic mechanisms of stress management and fidelity in a cell and organism.
References
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Journal ArticleDOI

Regulation of p53 by hypoxia: dissociation of transcriptional repression and apoptosis from p53-dependent transactivation.

TL;DR: It is reported that hypoxia induces p53 protein accumulation, but in contrast to DNA damage,Hypoxia fails to induce endogenous downstream p53 effector mRNAs and proteins, leading to a model in which different cellular pools of p53 can modulate transcriptional activity through interactions with transcriptional coactivators or corepressors.
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The polyproline region of p53 is required to activate apoptosis but not growth arrest.

TL;DR: It is concluded that p53's ability to induce apoptosis is dispensable for inhibiting cell growth and transformation and that the PP region plays a crucial role in apoptotic signaling.
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Hsp60 accelerates the maturation of pro-caspase-3 by upstream activator proteases during apoptosis

TL;DR: It is proposed that the ATP‐dependent ‘foldase’ activity of Hsp60 improves the vulnerability of pro‐caspase‐3 to proteolytic maturation by upstream caspases and that this represents an important regulatory event in apoptotic cell death.
Journal ArticleDOI

Nix and Nip3 Form a Subfamily of Pro-apoptotic Mitochondrial Proteins *

TL;DR: Nix is identified, a homolog of the E1B 19K/Bcl-2 binding and pro-apoptotic protein Nip3, and it is proposed that Nix and Nip 3 form a new subfamily of pro-APoptotic mitochondrial proteins.
Journal ArticleDOI

A variation in the structure of the protein-coding region of the human p53 gene

TL;DR: Molecular cloning and sequencing of both the alleles of p53 gene revealed a base-pair change in codon 72 causing arginine----proline substitution in the allele with the additional BglII site.
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