FORWARD GENETICS IN REVEALS GENETIC ADAPTATIONS TO POLYUNSATURATED FATTY ACID DEFICIENCY.

Polyunsaturated fatty acids (PUFAs) are essential for mammalian health and function as membrane fluidizers and precursors for signaling lipids though the primary essential function of PUFAs within organisms has not been established. Unlike mammals who cannot endogenously synthesize PUFAs, can synthesize PUFAs starting with the Δ12 desaturase FAT-2 which introduces a second double bond to monounsaturated fatty acids to generate the PUFA linoleic acid. FAT-2 desaturation is essential for survival since null mutants are non-viable; the near-null allele synthesizes only small amounts of PUFAs and produces extremely sick worms. Using fluorescence recovery after photobleaching (FRAP), we found that the mutant has rigid membranes and can be efficiently rescued by dietarily providing various PUFAs, but not by fluidizing treatments or mutations. With the aim of identifying mechanisms that compensate for PUFA-deficiency, we performed a forward genetics screen to isolate novel suppressors and identified four internal mutations within , and six mutations within the HIF-1 pathway. The suppressors increase PUFA levels in mutant worms and additionally suppress the activation of the , UPR and UPR stress response pathways that are active in worms. We hypothesize that the six HIF-1 pathway mutations, found in , , and all converge on raising Fe levels and in this way boost desaturase activity, including that of the allele. We conclude that PUFAs cannot be genetically replaced and that the only genetic mechanism that can alleviate PUFA-deficiency do so by increasing PUFA levels.