Abstract
Many cells require cilia to receive environmental signals. Mutations in the ciliary gene fam149b1 result in the ciliopathy Joubert syndrome. The C. elegans homolog of fam149b1 , xbx-4 , is required for normal cilium structure. We found that loss of XBX-4 hinders multiple cilium-mediated behaviors. xbx-4 mutants display mild defects in male mating and nose touch behaviors and dramatic changes in social feeding. Unexpectedly, xbx-4 mutants increased reversal behavior in response to ethanol, a control stimulus used in olfactory assays. Variation in the magnitude of phenotypes for different neurons is consistent with known cell-specific impacts of XBX-4 loss on cilium structure.