Abstract
The mechanisms that integrate genetic and environmental information to coordinate the expression of complex phenotypes are little understood. We investigated the role of two protein kinases (PKs) in the population density-dependent transition to gregarious behavior that underlies swarm formation in desert locusts: theforaginggene product, a cGMP-dependent PK (PKG) implicated in switching between alternative group-related behaviors in several animal species; and cAMP-dependent PK (PKA), a signal transduction protein with a preeminent role in different forms of learning. Solitarious locusts acquire key behavioral characters of the swarming gregarious phase within just 1 to 4 h of forced crowding. Injecting the PKA inhibitor KT5720 before crowding prevented this transition, whereas injecting KT5823, an inhibitor of PKG, did not. Neither drug altered the behavior of long-term gregarious locusts. RNAi againstforagingeffectively reduced its expression in the central nervous system, but this did not prevent gregarization upon crowding. By contrast, solitarious locusts with an RNAi-induced reduction in PKA catalytic subunit C1 expression behaved less gregariously after crowding, and RNAi against the inhibitory R1 subunit promoted more extensive gregarization following a brief crowding period. A central role of PKA is congruent with the recent discovery that serotonin mediates gregarization in locusts and with findings in vertebrates that similarly implicate PKA in the capacity to cope with adverse life events. Our results show that PKA has been coopted into effecting the wide-ranging transformation from solitarious to gregarious behavior, with PKA-mediated behavioral plasticity resulting in an environmentally driven reorganization of a complex phenotype.
Highlights
The mechanisms that integrate genetic and environmental information to coordinate the expression of complex phenotypes are little understood
To test for a role for protein kinase A (PKA) activity in this transition, we injected solitarious locusts (n = 23) with KT5720, a staurosporine/K525type inhibitor that competes for the ATP-binding site on the PKA catalytic subunits [38]
Locusts injected with KT5823 were as likely to show gregarious behavior as their matched controls (Pgreg = 0.723; t49 = 0.5964, P = 0.554), but those injected with KT5720 remained much more solitarious (Pgreg = 0.358; t43 = −3.0044, P = 0.00443)
Summary
The mechanisms that integrate genetic and environmental information to coordinate the expression of complex phenotypes are little understood. We investigated the role of two protein kinases (PKs) in the population density-dependent transition to gregarious behavior that underlies swarm formation in desert locusts: the foraging gene product, a cGMP-dependent PK (PKG) implicated in switching between alternative group-related behaviors in several animal species; and cAMP-dependent PK (PKA), a signal transduction protein with a preeminent role in different forms of learning. Our results show that PKA has been coopted into effecting the wide-ranging transformation from solitarious to gregarious behavior, with PKAmediated behavioral plasticity resulting in an environmentally driven reorganization of a complex phenotype. In solitarious locusts, gregarizing stimuli cause an increase in 5-HT in the thoracic ganglia, but with prolonged crowding, 5-HT decreases to lower than solitarious levels [16] This indicates that, after induction, gregariousness is maintained by other means, echoing the transient role of 5-HT in classical forms of learning.
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