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GCN5L1/BLOS1 Links Acetylation, Organelle Remodeling, and Metabolism

Journal

TRENDS IN CELL BIOLOGY
Volume 28, Issue 5, Pages 346-355

Publisher

ELSEVIER SCIENCE LONDON
DOI: 10.1016/j.tcb.2018.01.007

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Funding

  1. American Diabetes Association [1-17-IBS-197]
  2. NHLBI [K22-HL116728, R56-HL132917, R01-HL132917, HL006047-06, HL005102-11]

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General control of amino acid synthesis 5 (GCN5) like-1 (GCN5L1) was identified as a novel gene with sequence homology to the histone acetyltransferase Gcn5. Subsequent protein-interaction studies identified GCN5L1 as a subunit of the multiprotein lysosome biogenesis complex, resulting in an alternative designation as biogenesis of lysosome-related organelle complex 1 subunit 1 (BLOS1 or BLOC1S1). Despite the distinct nomenclatures, GCN5L1/BLOS1 has been shown to play crucial roles in mitochondria, endosomes, lysosomes, and synaptic vesicle precursors (SVPs). GCN5L1/BLOS1 controls mitochondrial protein acetylation, modulates metabolic pathways, and orchestrates retrograde mitochondria-to-nucleus signaling. It also contributes to endosome-lysosome and vesicle trafficking and to endolysosomal function. Here we discuss the intracellular roles of GCN5L1/BLOS1 in the hope of linking mitochondria-centric effects to cytosolic vesicle biology.

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