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Significance Endosomes are membrane-bound organelles that are important for nutrient uptake, protein and lipid sorting, and signal transduction. When integral membrane proteins have reached the endosomal system, they can be sent to the lysosome for degradation or recycled for reuse. Here we provide insight into how the machinery important for reuse controls the machinery that mediates degradation. We show that these opposing functions occupy physically distinct regions of the endosomes, termed microdomains, and that this separation is likely to provide a physical framework for a variety of sorting decisions.

SNX-1 and RME-8 oppose the assembly of HGRS-1/ESCRT-0 degradative microdomains on endosomes