BBSome regulation of LITE-1 receptor in a cilium-independent manner in C. elegans

Bardet-Biedl Syndrome (BBS) is a genetic disorder affecting primary cilia. BBSome, a protein complex composed of eight BBS proteins, regulates the structure and function of cilia in diverse organisms, and its malfunction causes BBS in humans. Here, we report a new function of BBSome in C. elegans. In a forward genetic screen for genes regulating the light sensitivity of the ciliated ASH sensory neurons, we isolated bbs mutants, indicating that BBSome regulates ASH photosensitivity. Surprisingly, cilia are not required for ASH neurons to sense light, suggesting that BBSome regulates ASH photosensitivity independently of cilia. Interestingly, the light-sensing receptor LITE-1, which mediates photosensation, is a non-ciliary protein in ASH neurons. LITE-1 in ASH neurons becomes unstable in bbs mutants in an age-dependent manner, indicating that BBSome regulates the stability of LITE-1 in these neurons. These results identify a cilium-independent function of BBSome in regulating a non-ciliary protein in ciliated cells.