Proximity-based proteomics (BioID) uncovers the Rho GTPase interactome in kidney podocytes

Our BioID analysis detected a total of 1927 interactions with AvgP ≥ 0.95. Approximately 50% of the interactions are unique to podocytes compared to interactions in HEK293 and HeLa cells, with enrichment in pathways related to cell adhesion and shape organization. <i>KIAA1522</i> emerged as a Rac1/Cdc42 interactor. <i>KIAA1522</i> knockout reduced cellular projection formation in podocytes, while <i>KIAA1522</i> knockdown in zebrafish resulted in foot process effacement. Additionally, we identified 20 guanine nucleotide exchange factors (GEFs), with 11, 8, and 5 interacting with RhoA, Rac1, and Cdc42, respectively. Analysis of public scRNA-seq datasets identified RhoA regulators as highly enriched in podocytes. Knockout of most RhoA GEFs reduced RhoA activity, with ARHGEF12 having the greatest effect. Our study defined key upstream regulators and downstream effectors of Rho GTPases in podocytes, identifying <i>KIAA1522</i> as a novel Cdc42 effector and ARHGEF12 as a key RhoA regulator.