Please use this identifier to cite or link to this item: https://doi.org/10.1038/srep33972
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dc.titleFunctional characterization of p53 pathway components in the ancient metazoan Trichoplax adhaerens
dc.contributor.authorSiau, J.W
dc.contributor.authorCoffill, C.R
dc.contributor.authorZhang, W.V
dc.contributor.authorTan, Y.S
dc.contributor.authorHundt, J
dc.contributor.authorLane, D
dc.contributor.authorVerma, C
dc.contributor.authorGhadessy, F
dc.date.accessioned2020-10-22T02:48:48Z
dc.date.available2020-10-22T02:48:48Z
dc.date.issued2016
dc.identifier.citationSiau, J.W, Coffill, C.R, Zhang, W.V, Tan, Y.S, Hundt, J, Lane, D, Verma, C, Ghadessy, F (2016). Functional characterization of p53 pathway components in the ancient metazoan Trichoplax adhaerens. Scientific Reports 6 : 33972. ScholarBank@NUS Repository. https://doi.org/10.1038/srep33972
dc.identifier.issn20452322
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/178860
dc.description.abstractThe 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.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.typeArticle
dc.contributor.departmentMEDICINE
dc.contributor.departmentBIOLOGY (NU)
dc.description.doi10.1038/srep33972
dc.description.sourcetitleScientific Reports
dc.description.volume6
dc.description.page33972
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