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?Np63? represses nuclear translocation of PTEN by inhibition of NEDD4-1 in keratinocytes.


ABSTRACT: ?Np63? maintains the proliferative potential of keratinocytes by inhibiting the transcription and nuclear localization of the tumor suppressor PTEN as shown earlier by our laboratory. The goal of this study was to define the mechanisms by which ?Np63? mediates the nuclear exclusion of PTEN. We demonstrate here that ?Np63? reduces the ubiquitination of PTEN, a key signaling event in the nuclear translocation of PTEN. The decrease in ubiquitinated PTEN correlated with the ability of ?Np63? to bind to neuronal precursor developmentally down regulated 4 (NEDD4) promoter and transcriptionally repress the E3 ubiquitin ligase NEDD4-1. Knockdown of NEDD4-1 in cultured keratinocytes was sufficient to attenuate the increase in nuclear PTEN observed upon silencing of ?Np63?. In vivo examination of normal skin demonstrated that ?Np63? and NEDD4-1 were both expressed in the basal layer of the epidermis and this correlated with nuclear exclusion of PTEN. Altogether, these studies suggest that ?Np63?-mediated suppression of nuclear PTEN in basal layer keratinocytes occurs through repression of NEDD4-1.

SUBMITTER: Leonard MK 

PROVIDER: S-EPMC3779491 | biostudies-literature | 2013 Oct

REPOSITORIES: biostudies-literature

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ΔNp63α represses nuclear translocation of PTEN by inhibition of NEDD4-1 in keratinocytes.

Leonard Mary K MK   Hill Natasha T NT   Grant Ethan D ED   Kadakia Madhavi P MP  

Archives of dermatological research 20130416 8


ΔNp63α maintains the proliferative potential of keratinocytes by inhibiting the transcription and nuclear localization of the tumor suppressor PTEN as shown earlier by our laboratory. The goal of this study was to define the mechanisms by which ΔNp63α mediates the nuclear exclusion of PTEN. We demonstrate here that ΔNp63α reduces the ubiquitination of PTEN, a key signaling event in the nuclear translocation of PTEN. The decrease in ubiquitinated PTEN correlated with the ability of ΔNp63α to bind  ...[more]

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