TY - JOUR
T1 - A longitudinal study of caenorhabditis elegans larvae reveals a novel locomotion switch, regulated by gαs signaling
AU - Nagy, Stanislav
AU - Wright, Charles
AU - Tramm, Nora
AU - Labello, Nicholas
AU - Burov, Stanislav
AU - Biron, David
PY - 2013/7/2
Y1 - 2013/7/2
N2 - Despite their simplicity, longitudinal studies of invertebrate models are rare. We thus sought to characterize behavioral trends of Caenorhabditis elegans, from the mid fourth larval stage through the mid young adult stage. We found that, outside of lethargus, animals exhibited abrupt switching between two distinct behavioral states: active wakefulness and quiet wakefulness. The durations of epochs of active wakefulness exhibited non-Poisson statistics. Increased Gαs signaling stabilized the active wakefulness state before, during and after lethargus. In contrast, decreased Gαs signaling, decreased neuropeptide release, or decreased CREB activity destabilized active wakefulness outside of, but not during, lethargus. Taken together, our fndings support a model in which protein kinase A (PKA) stabilizes active wakefulness, at least in part through two of its downstream targets: neuropeptide release and CREB. However, during lethargus, when active wakefulness is strongly suppressed, the native role of PKA signaling in modulating locomotion and quiescence may be minor.
AB - Despite their simplicity, longitudinal studies of invertebrate models are rare. We thus sought to characterize behavioral trends of Caenorhabditis elegans, from the mid fourth larval stage through the mid young adult stage. We found that, outside of lethargus, animals exhibited abrupt switching between two distinct behavioral states: active wakefulness and quiet wakefulness. The durations of epochs of active wakefulness exhibited non-Poisson statistics. Increased Gαs signaling stabilized the active wakefulness state before, during and after lethargus. In contrast, decreased Gαs signaling, decreased neuropeptide release, or decreased CREB activity destabilized active wakefulness outside of, but not during, lethargus. Taken together, our fndings support a model in which protein kinase A (PKA) stabilizes active wakefulness, at least in part through two of its downstream targets: neuropeptide release and CREB. However, during lethargus, when active wakefulness is strongly suppressed, the native role of PKA signaling in modulating locomotion and quiescence may be minor.
UR - http://www.scopus.com/inward/record.url?scp=84881527710&partnerID=8YFLogxK
U2 - 10.7554/eLife.00782
DO - 10.7554/eLife.00782
M3 - Article
C2 - 23840929
AN - SCOPUS:84881527710
SN - 2050-084X
VL - 2013
JO - eLife
JF - eLife
IS - 2
M1 - e00782
ER -