We previously discovered an autophagy‐like proteolysis mechanism that uses the Golgi membrane, namely, Golgi membrane‐associated degradation (GOMED). Morphologically, GOMED resembles canonical autophagy, but the two mechanisms have different cellular functions, as they degrade different substrates and use different membrane sources. Furthermore, although the molecules involved partially overlap, the core molecules are completely different. GOMED preferentially degrades Golgi‐trafficking proteins, including insulin granules in pancreatic β‐cells and ceruloplasmin in neurons, and is involved in a wide variety of physiological events.
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