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Updated: Dec 27, 2025

Study of Protein-protein Interactions in Autophagy Research
Published on: September 9, 2017
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.
Abstract:
To resolve the signaling mechanisms that mediate the starvation-induced processes of Dictyostelium sporulation and encystation, we performed insertional mutagenesis on cells harboring an mRFP-tagged spore gene. We isolated a mutant in kinkyA (knkA), a gene without known function, which formed fruiting bodies with a kinked stalk and lacking viable spores. Immunoprecipitation of lysates of KnkA-YFP-transformed knkA cells yielded a mammalian BCAS3 homolog as a KnkA interactor. bcas3 phenocopied knkA and Bcas3 colocalized with KnkA to puncta. Bcas3 shares sequence similarity with proppins (beta-propellors that bind phosphoinositides). Mutation of 2 Bcas3 residues that are essential for PtdIns3P binding in proppins prevented Bcas3 binding to PtdIns3P as well as punctate Bcas3 and KnkA localization. KnkA puncta also colocalized with small but not large vesicles that contain the autophagy protein Atg8 and were contiguous with the endoplasmic reticulum. knkA and bcas3 cells showed a pronounced decrease of RFP-GFP-Atg8 in neutral early autophagosomes, indicating that KnkA and Bcas3 are required for macroautophagy/autophagy. Knockouts in atg7, atg5 or atg9 substantiated this finding by showing similar sporulation defects as knkA and bcas3. Defective Dictyostelium sporulation is evidently a useful diagnostic tool for the discovery of novel autophagy genes.Abbreviations: Atg: Autophagy-related; BCAS3: BCAS3 microtubule associated cell migration factor; cAMP: 3',5'-cyclic adenosine monophosphate; ER: endoplasmic reticulum; GFP: green fluorescent protein; PAS: phagophore assembly site; PRKA/PKA: protein kinase cAMP-dependent; Proppin: beta-propellers that bind phosphoinositides; PtdIns3P: phosphatidylinositol 3-phosphate; REMI: restriction enzyme-mediated insertional mutagenesis; RFP: red fluorescent protein; RT-qPCR: reverse transcriptase - quantitative polymerase chain reaction; WIPI: WD repeat domain, phosphoinositide interacting; YFP: yellow fluorescent protein.
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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