The ETS-5 transcription factor regulates activity states in Caenorhabditis elegans by controlling satiety.
Vaida JuozaityteDavid Pladevall-MoreraAgnieszka PodolskaSteffen NørgaardBrent NeumannRoger PocockPublished in: Proceedings of the National Academy of Sciences of the United States of America (2017)
Animal behavior is shaped through interplay among genes, the environment, and previous experience. As in mammals, satiety signals induce quiescence in Caenorhabditis elegans Here we report that the C. elegans transcription factor ETS-5, an ortholog of mammalian FEV/Pet1, controls satiety-induced quiescence. Nutritional status has a major influence on C. elegans behavior. When foraging, food availability controls behavioral state switching between active (roaming) and sedentary (dwelling) states; however, when provided with high-quality food, C. elegans become sated and enter quiescence. We show that ETS-5 acts to promote roaming and inhibit quiescence by setting the internal "satiety quotient" through fat regulation. Acting from the ASG and BAG sensory neurons, we show that ETS-5 functions in a complex network with serotonergic and neuropeptide signaling pathways to control food-regulated behavioral state switching. Taken together, our results identify a neuronal mechanism for controlling intestinal fat stores and organismal behavioral states in C. elegans, and establish a paradigm for the elucidation of obesity-relevant mechanisms.
Keyphrases
- transcription factor
- genome wide identification
- dna binding
- adipose tissue
- human health
- signaling pathway
- type diabetes
- metabolic syndrome
- physical activity
- insulin resistance
- weight loss
- computed tomography
- genome wide
- spinal cord
- risk assessment
- high glucose
- positron emission tomography
- diabetic rats
- high fat diet induced
- gene expression
- climate change
- skeletal muscle
- drug induced
- brain injury
- oxidative stress
- cell proliferation
- subarachnoid hemorrhage