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Functional characterization of p53 pathway components in the ancient metazoan Trichoplax adhaerens.


ABSTRACT: The identification of genes encoding a p53 family member and an Mdm2 ortholog in the ancient placozoan Trichoplax adhaerens advocates for the evolutionary conservation of a pivotal stress-response pathway observed in all higher eukaryotes. Here, we recapitulate several key functionalities ascribed to this known interacting protein pair by analysis of the placozoan proteins (Tap53 and TaMdm2) using both in vitro and cellular assays. In addition to interacting with each other, the Tap53 and TaMdm2 proteins are also able to respectively bind human Mdm2 and p53, providing strong evidence for functional conservation. The key p53-degrading function of Mdm2 is also conserved in TaMdm2. Tap53 retained DNA binding associated with p53 transcription activation function. However, it lacked transactivation function in reporter genes assays using a heterologous cell line, suggesting a cofactor incompatibility. Overall, the data supports functional roles for TaMdm2 and Tap53, and further defines the p53 pathway as an evolutionary conserved fulcrum mediating cellular response to stress.

SUBMITTER: Siau JW 

PROVIDER: S-EPMC5039725 | biostudies-literature | 2016 Sep

REPOSITORIES: biostudies-literature

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Functional characterization of p53 pathway components in the ancient metazoan Trichoplax adhaerens.

Siau Jia Wei JW   Coffill Cynthia R CR   Zhang Weiyun Villien WV   Tan Yaw Sing YS   Hundt Juliane J   Lane David D   Verma Chandra C   Ghadessy Farid F  

Scientific reports 20160928


The identification of genes encoding a p53 family member and an Mdm2 ortholog in the ancient placozoan Trichoplax adhaerens advocates for the evolutionary conservation of a pivotal stress-response pathway observed in all higher eukaryotes. Here, we recapitulate several key functionalities ascribed to this known interacting protein pair by analysis of the placozoan proteins (Tap53 and TaMdm2) using both in vitro and cellular assays. In addition to interacting with each other, the Tap53 and TaMdm2  ...[more]

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