Literature DB >> 31519766

BioID Performed on Golgi Enriched Fractions Identify C10orf76 as a GBF1 Binding Protein Essential for Golgi Maintenance and Secretion.

Calvin J Chan1, Roberta Le1, Kaylan Burns1, Khadra Ahmed1, Etienne Coyaud2, Estelle M N Laurent2, Brian Raught2, Paul Melançon3.   

Abstract

The Golgi-specific Brefeldin-A resistance factor 1 (GBF1) is the only large GEF that regulates Arf activation at the cis-Golgi and is actively recruited to membranes on an increase in Arf-GDP. Recent studies have revealed that GBF1 recruitment requires one or more heat-labile and protease-sensitive protein factor(s) (Quilty et al., 2018, J. Cell Science, 132). Proximity-dependent biotinylation (BioID) and mass spectrometry from enriched Golgi fractions identified GBF1 proximal proteins that may regulate its recruitment. Knockdown studies revealed C10orf76 to be involved in Golgi maintenance. We find that C10orf76 interacts with GBF1 and rapidly cycles on and off GBF1-positive Golgi structures. More importantly, its depletion causes Golgi fragmentation, alters GBF1 recruitment, and impairs secretion. Homologs were identified in most species, suggesting its presence in the last eukaryotic common ancestor.
© 2019 Chan et al.

Entities:  

Keywords:  BioID; Cell biology; GBF1; GTPase; biotin; cell secretion; cellular organelles; golgi; imaging; membranes; secretome

Mesh:

Substances:

Year:  2019        PMID: 31519766      PMCID: PMC6823846          DOI: 10.1074/mcp.RA119.001645

Source DB:  PubMed          Journal:  Mol Cell Proteomics        ISSN: 1535-9476            Impact factor:   5.911


  41 in total

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