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. 2016 Nov 15;27(23):3780–3790. doi: 10.1091/mbc.E16-03-0189

FIGURE 2:

FIGURE 2:

Nonciliary Arl13bV358A mutant is defective in Shh-stimulated MEF migration despite Arl13bV358A being biochemically indistinguishable from wild-type Arl13b protein. (A) Average total migration for Arl13bhnn MEFs expressing Arl13b-GFP mutants, normalized to wild-type Arl13b-GFP, migrating toward rShhN. N = 12. Analysis described in Materials and Methods. (B) Recombinant mouse Arl13b and Arl13bV358A display indistinguishable intrinsic and GAP-stimulated rates of GTP hydrolysis. (C) Arl13bhnn MEFs expressing GFP or Arl13bWT-GFP, normalized to the GFP-only control, migrate similarly toward fetal calf serum (FCS). (D) Arl13bhnn MEFs expressing GFP show impaired migration toward the Smo agonist purmorphamine, which can be rescued by Arl13bWT-GFP.