AMP-activated protein kinase (AMPK) is a key metabolic regulator which responds to changes in the AMP:ATP ratio within
cells. In response to high AMP levels, AMPK promotes a metabolic shift towards increased catabolism and autophagy to
restore cellular energy and maintain homeostasis. In C. elegans, AMPK is important for controlling a multitude of functions
including metabolism, reproductive health, and lifespan. AMPK is a heterotrimeric protein consisting of α catalytic, β linker,
and γ regulatory subunits. Active AMPK is characterised by phosphorylation of the α subunit. It is also regulated allosterically
by the nucleotide AMP binding within the γ subunit. C. elegans have five different AMPKγ subunits and their primary amino
acid sequence implies two different modes of AMP-binding. Modifying the ability of AMPKγ to bind adenine nucleotides
could directly impact how effectively AMPK manages energy homeostasis. Despite the importance of the γ subunit, most C.
elegans AMPK research has focused on the catalytic α subunit. Here, we genetically dissect the functional role of the different
γ subunits in relation to physiology and lifespan. We show that in normal animals, three of these γ subunits (aakg-1, aakg-2,
and aakg-3) are required for normal responses to AMP, and contribute to normal fecundity and lifespan
