The proppin Bcas3 and its interactor KinkyA localize to the early phagophore and regulate autophagy

Yoko Yamada1,2, Pauline Schaap1

  • 1School of Life Sciences, University of Dundee, Dundee, UK.

Autophagy
|March 3, 2020
PubMed

Insights

Researchers identified KinkyA (KnkA) and BCAS3 as crucial for Dictyostelium sporulation and autophagy. These proteins interact and are essential for autophagosome formation during starvation-induced processes.

Area of Science:

  • Cell Biology
  • Molecular Biology
  • Developmental Biology

Background:

  • Starvation triggers Dictyostelium sporulation and encystation through complex signaling pathways.
  • Understanding these mechanisms is key to deciphering cellular differentiation and survival strategies.

Purpose of the Study:

  • To identify novel genes involved in starvation-induced Dictyostelium sporulation and encystation.
  • To elucidate the signaling mechanisms underlying these developmental processes.

Main Methods:

  • Insertional mutagenesis using mRFP-tagged spore gene in Dictyostelium.
  • Immunoprecipitation to identify protein interactors of KinkyA (KnkA).
  • Phenotypic analysis of mutants, including sporulation assays and protein localization studies using YFP-tagged proteins.

Main Results:

  • A mutant in the uncharacterized gene kinkyA (knkA) exhibited defective sporulation with kinked stalks and no viable spores.
  • KnkA interacts with a mammalian BCAS3 homolog (Bcas3), which phenocopied knkA mutations.
  • KnkA and Bcas3 localize to puncta, require phosphatidylinositol 3-phosphate (PtdIns3P) binding for localization, and are essential for autophagosome formation, as evidenced by decreased RFP-GFP-Atg8 in autophagosomes.
  • KnkA and Bcas3 are required for macroautophagy/autophagy, as confirmed by sporulation defects in atg7, atg5, and atg9 knockouts.

Conclusions:

  • KinkyA (KnkA) and BCAS3 are novel essential regulators of Dictyostelium sporulation and autophagy.
  • Defective sporulation serves as a valuable screen for identifying new autophagy-related genes.
  • The findings reveal a role for KnkA and Bcas3 in PtdIns3P-dependent autophagosome biogenesis during starvation response.

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