Citation
- Authors: Dewees SI. et al.
- Year: 2022
- Journal: Mol Biol Cell 33 ar33
- Applications: in vitro / DNA / jetOPTIMUS
- Cell type: MEF
Description: Murine embryonic fibroblast cells
Method
Cells were transfected with 4 µg DNA: 4 µL JetOPTIMUS transfection reagent according to manufacturer guidelines in standard medium overnight.
The next day, cells were replated on coverslips in standard medium and allowed to recover for 24 hr. Cells were then serum starved for 24-72 hr to induce ciliation prior to fixation.
Abstract
The ARF family of regulatory GTPases is ancient, with 16 members predicted to have been present in the last eukaryotic common ancestor. Our phylogenetic profiling of paralogues in diverse species identified four family members whose presence correlates with that of a cilium/flagellum: ARL3, ARL6, ARL13, and ARL16. No prior evidence links ARL16 to cilia or other cell functions, despite its presence throughout eukaryotes. Deletion of ARL16 in mouse embryonic fibroblasts (MEFs) results in decreased ciliogenesis yet increased ciliary length. We also found Arl16 knockout (KO) in MEFs to alter ciliary protein content, including loss of ARL13B, ARL3, INPP5E, and the IFT-A core component IFT140. Instead, both INPP5E and IFT140 accumulate at the Golgi in Arl16 KO lines, while other intraflagellar transport (IFT) proteins do not, suggesting a specific defect in traffic from Golgi to cilia. We propose that ARL16 regulates a Golgi-cilia traffic pathway and is required specifically in the export of IFT140 and INPP5E from the Golgi.