A lateralized sensory signaling pathway mediates context-dependent olfactory plasticity in <i>Caenorhabditis elegans</i>

Lateralization of neuronal functions plays a critical role in regulating behavioral flexibility, but the underlying molecular mechanisms are challenging to establish at a single-neuron level. We previously showed that attraction of <i>Caenorhabditis elegans</i> to a medium-chain alcohol switches to avoidance in a uniform background of a second attractive odorant. This context-dependent behavioral plasticity is mediated by symmetric inversion of the odor-evoked response sign in the bilateral AWC olfactory neurons. Here, we show that this symmetric response plasticity is driven by asymmetric molecular mechanisms in the AWC neuron pair. Mutations in the <i>gcy-12</i> receptor guanylyl cyclase abolish odor response plasticity only in AWC^OFF; the opposite odor-evoked response signs in AWC^OFF and AWC^ON in <i>gcy-12</i> mutants result in these animals being behaviorally indifferent to this chemical. We find that <i>gcy-12</i> is expressed, and required, in both AWC neurons to regulate odor response plasticity only in AWC^OFF. We further show that disruption of AWC fate lateralization results in loss of asymmetry in the response plasticity in <i>gcy-12</i> mutants. Our results indicate that symmetric neuronal response plasticity can arise from asymmetric underlying molecular mechanisms and suggest that lateralization of signaling pathways in defined conditions may enhance neuronal and behavioral flexibility.