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. 2009 Jan 9;284(2):1213–1223. doi: 10.1074/jbc.M805957200

FIGURE 5.

FIGURE 5.

Myosin Va and myosin Vb tails alter endogenous Rab11a distribution in an exon-independent manner. A and B, HeLa cells transfected with EGFP-myosin Va tail +D or EGFP-myosin Va tail -D and stained for endogenous Rab11a. Unlike Rab8a and Rab10, Rab11a co-localized with both splice isoforms of myosin Va tail in scattered puncta. C and D, similarly, expression of either splice isoform of EGFP-myosin Vb tail (+Dor -D) caused endogenous Rab11a to localize to the EGFP-labeled perinuclear cisterna. Scale bars in all panels represent 10 μm. Percent co-localization (±S.E.) are listed in the merged images on the right of each panel (n ≥ 10).