Abstract
Rab GTPases are key regulators of membrane traffic. The Rab GTPase Ypt1 is essential for endoplasmic reticulum (ER)-Golgi traffic, intra-Golgi traffic, and the macroautophagy pathway. To identify effectors on the macroautophagy pathway, known autophagy-related genes (Atg genes) required for macroautophagy were tagged with GFP and screened for mislocalization in the ypt1-2 mutant. At the pre-autophagosomal structure (PAS), the localization of the serine/threonine kinase Atg1 was affected in the ypt1-2 mutant. We then used an in vitro binding assay to determine if Atg1 and Ypt1 physically interact with each other and co-immunoprecipitation experiments were performed to address if Atg1 preferentially interacts with the GTP-bound form of Ypt1.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Autophagy*
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Autophagy-Related Proteins
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Glutathione / chemistry
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Guanosine Triphosphate / metabolism
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Immunoprecipitation
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Microscopy, Fluorescence
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Mutation
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Phagosomes / metabolism
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Protein Interaction Mapping / methods*
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Protein Kinases / isolation & purification
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Protein Kinases / metabolism
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Protein Transport
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Saccharomyces cerevisiae / cytology
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Saccharomyces cerevisiae / genetics
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Saccharomyces cerevisiae / metabolism
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Saccharomyces cerevisiae Proteins / genetics
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Saccharomyces cerevisiae Proteins / isolation & purification
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Saccharomyces cerevisiae Proteins / metabolism
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Sepharose / chemistry
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rab GTP-Binding Proteins / genetics
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rab GTP-Binding Proteins / isolation & purification
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rab GTP-Binding Proteins / metabolism*
Substances
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Autophagy-Related Proteins
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Saccharomyces cerevisiae Proteins
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Guanosine Triphosphate
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Sepharose
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Protein Kinases
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ATG1 protein, S cerevisiae
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YPT1 protein, S cerevisiae
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rab GTP-Binding Proteins
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Glutathione