A Novel Role for Polycystin-2 (Pkd2) in as a Probable Mg Channel Necessary for Mg-Induced Behavior.

A human ciliopathy gene codes for Polycystin-2 (Pkd2), a non-selective cation channel. Here, the Pkd2 channel was explored in the ciliate using combinations of RNA interference, over-expression, and epitope-tagging, in a search for function and novel interacting partners. Upon depletion of Pkd2, cells exhibited a phenotype similar to (XntA1), a mutant lacking the inward Ca-dependent Mg conductance. Further investigation showed both Pkd2 and XntA localize to the cilia and cell membrane, but do not require one another for trafficking. The XntA-myc protein co-immunoprecipitates Pkd2-FLAG, but not vice versa, suggesting two populations of Pkd2-FLAG, one of which interacts with XntA. Electrophysiology data showed that depletion and over-expression of Pkd2 led to smaller and larger depolarizations in Mg solutions, respectively. Over-expression of Pkd2-FLAG in the XntA1 mutant caused slower swimming, supporting an increase in Mg permeability, in agreement with the electrophysiology data. We propose that Pkd2 in collaborates with XntA for Mg-induced behavior. Our data suggest Pkd2 is sufficient and necessary for Mg conductance and membrane permeability to Mg, and that Pkd2 is potentially a Mg-permeable channel.