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Critical role for protein kinase A in the acquisition of gregarious behavior in the desert locust

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posted on 2014-11-12, 14:35 authored by Swidbert R. Ott, Heleen Verlinden, Stephen M. Rogers, Caroline H. Brighton, Pei Shan Quah, Rut K. Vleugels, Rik Verdonck, Jozef Vanden Broeck
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. 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 against foraging effectively 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.

History

Citation

Proceedings of the National Academy of Sciences U S A, 2012, 109 (7), pp. E381-E387

Author affiliation

/Organisation/COLLEGE OF MEDICINE, BIOLOGICAL SCIENCES AND PSYCHOLOGY/School of Biological Sciences/Department of Biology

Version

  • AM (Accepted Manuscript)

Published in

Proceedings of the National Academy of Sciences U S A

Publisher

National Academy of Sciences

eissn

1091-6490

Copyright date

2014

Available date

2014-11-12

Publisher version

http://www.pnas.org/content/109/7/E381.full.pdf+html

Language

en

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