Identification of a WNT5A-responsive degradation domain in the kinesin superfamily protein KIF26B

Edith P. Karuna, Shannon S. Choi, Michael K. Scales, Jennie Hum, Michael Cohen, Fernando A Fierro, Hsin-Yi Henry Ho

Research output: Contribution to journalArticle

2 Scopus citations

Abstract

Noncanonical WNT pathways function independently of the β-catenin transcriptional co-activator to regulate diverse morphogenetic and pathogenic processes. Recent studies showed that noncanonical WNTs, such as WNT5A, can signal the degradation of several downstream effectors, thereby modulating these effectors’ cellular activities. The protein domain(s) that mediates the WNT5A-dependent degradation response, however, has not been identified. By coupling protein mutagenesis experiments with a flow cytometry-based degradation reporter assay, we have defined a protein domain in the kinesin superfamily protein KIF26B that is essential for WNT5A-dependent degradation. We found that a human disease-causing KIF26B mutation located at a conserved amino acid within this domain compromises the ability of WNT5A to induce KIF26B degradation. Using pharmacological perturbation, we further uncovered a role of glycogen synthase kinase 3 (GSK3) in WNT5A regulation of KIF26B degradation. Lastly, based on the identification of the WNT5A-responsive domain, we developed a new reporter system that allows for efficient profiling of WNT5A-KIF26B signaling activity in both somatic and stem cells. In conclusion, our study identifies a new protein domain that mediates WNT5A-dependent degradation of KIF26B and provides a new tool for functional characterization of noncanonical WNT5A signaling in cells.

Original languageEnglish (US)
Article number196
JournalGenes
Volume9
Issue number4
DOIs
StatePublished - Apr 1 2018

Keywords

  • Dishevelled
  • Frizzled receptors
  • GSK3
  • KIF26B
  • Mesenchymal stem cells
  • Protein degradation
  • ROR receptors
  • WNT5A

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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