Avl9は多様な細胞生物学的機能を調節するGTPアーゼ活性化タンパク質のファミリーを定義する
Abstract:
Ras-related GTPases are molecular switches regulating hundreds of signaling and trafficking pathways in cells. Many GTPase regulators remain to be identified despite extensive genetic and biochemical screens. Here we present the results of computational protein-protein interaction screens and functional experiments identifying the DENN domain protein Avl9 as a GTPase-activating protein for Arf1. Avl9 is involved in secretion and cell migration, but its molecular function has not been characterized. We determined that Avl9 possesses robust Arf-GAP activity and is recruited to secretory vesicles by Rab8. We find that Avl9 function is conserved in humans and enhances cell migration. We propose that several other DENN domain proteins are also candidate GAPs, and we demonstrate that one candidate previously characterized as a Rab-GEF, DENND6A, exhibits strong Arf-GAP activity towards ARL8B, explaining its role in lysosome positioning. Collectively, this work uncovers a family of monomeric 'DENN GAP' proteins that regulate diverse cell biological pathways.
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GTPases and their Regulation
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GTPases and their Regulation
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Small GTPases - Ras and Rho
Three regulatory proteins control their activity:
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Rab proteins switch between a cytosolic, GDP-bound inactive state and a membrane-anchored, GTP-bound active state. By themselves, Rabs show slow rates of GDP/GTP exchange and GTP hydrolysis. Thus, Rab proteins are considered...
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