Summary
Lipid droplets (LDs) are transient lipid storage organelles that can be readily tapped to resupply cells with energy or lipid building blocks, and therefore play a central role in cellular metabolism. However, the molecular factors and underlying mechanisms that regulate the growth and degradation of LDs are poorly understood. It has emerged that LD metabolism is sensitive to the autophagy- and LD-associated protein Double FYVE Domain Containing Protein 1 (DFCP1), however, little is known about DFCP1’s roles in autophagy and LD metabolism. Here, we show that DFCP1 contains a novel GTPase domain that regulates LD size by controlling the assembly of DFCP1 onto LDs in response to changes in nutrient availability. Specifically, we show that DFCP1 accumulation on LDs is independent of PI3P-binding, but requires a combination of the ER-binding domain and a unique GTPase domain. This novel GTPase domain possesses a low basal GTP turnover rate and has the ability to dimerize. Furthermore, mutations in the DFCP1 that either impact GTP hydrolysis or dimerization, result in changes in the accumulation of DFCP1 on LDs, as well as in changes in LD density and size. Importantly, the magnitude of these changes depends on the nutritional status of the cell. Collectively, our findings indicate that DFCP1 is a GTP-dependent metabolic sensor capable of modulating cellular storage of free fatty acids.
Competing Interest Statement
The authors have declared no competing interest.
