MGRN1-dependent pigment-type switching requires its ubiquitination activity but not its interaction with TSG101 or NEDD4

Teresa M. Gunn, Derek Silvius, Pooneh Bagher, Kaihua Sun, Katherine K. Walker

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

Mice lacking the E3 ubiquitin ligase mahogunin ring finger-1 (MGRN1) have a pleiotropic phenotype that includes spongiform neurodegeneration, embryonic patterning defects, and dark fur due to a defect in pigment-type switching. The only MGRN1 ubiquitination target identified to date is tumor susceptibility gene 101 (TSG101), a component of the endosomal trafficking machinery. Here, we show that MGRN1 also interacts with but does not ubiquitinate NEDD4, a HECT-domain ubiquitin ligase involved in endosomal trafficking. Using transgenesis in mice, we demonstrate that pigment-type switching likely requires MGRN1′s ubiquitin ligase activity but not its ability to bind TSG101 or NEDD4. This indicates that MGRN1-dependent ubiquitination of an as-yet unidentified target protein is required for agouti-mediated melanocortin signaling.

Original languageEnglish (US)
Pages (from-to)263-268
Number of pages6
JournalPigment Cell and Melanoma Research
Volume26
Issue number2
DOIs
StatePublished - Mar 2013
Externally publishedYes

Keywords

  • Agouti
  • Mahogunin ring finger-1 (MGRN1)
  • Melanocortin signaling
  • NEDD4
  • Pigment-type switching
  • TSG101

ASJC Scopus subject areas

  • Oncology
  • Biochemistry, Genetics and Molecular Biology(all)
  • Dermatology

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