“…Genetic studies of orthologues in lower eukaryotes suggest that the system arose as a Abbreviations: ACC, acetyl-CoA carboxylase; AgRP, agouti-related peptide; AICAR, 5-aminoimidazole-4-carboxamide riboside; AMPK, AMP-activated protein kinase; AS160, Akt substrate of 160 kDa; CaMKK, calmodulin-dependent protein kinase kinase; CBS1-4, cystathionine b-synthase motif 1-4; GLUT4, glucose transporter-4; IRS1, insulin receptor substrate-1; MC4, melanocortin-4; OCT1, organic cation transporter-1; PGC-1a, peroxisome proliferator-activated receptor-c co-activator-1a; POMC, pro-opiomelanocortin; PPAR-c, peroxisome proliferator-activated receptor-c; TSC, tuberous sclerosis complex protective mechanism that allows the organism to survive periods of starvation. The S. cerevisiae orthologue (the SNF1 complex) is required for the response to starvation for its preferred carbon source (glucose) and switches on expression of genes required for metabolism of other carbon sources [4]. It is also required for sporulation, which allows the organism to withstand a period of prolonged starvation.…”