Murphy and Montell. Vol. 133, No. 3, May 1996. Pages 617–630.
A corrected Table II and legend to Fig. 5 appear below.
Figure 5. Changes in F-actin distribution during normal border cell migration and effects of altered Rho proteins on border cells. (A and K) Wild-type stage 10 egg chambers stained for F-actin. (B) Nomarski optics image of slbo1/CyO stage 10 egg chamber stained for β-galactosidase activity. (C) High power confocal micrographs of wild-type border cells initiating migration in stage 9 (C) and after migration in stage 10 (D), stained for F-actin. The triangle indicates one filopodium in C. C and D are high power images of the same egg chambers shown in Fig. 1, H and I. (E) F-actin staining of a representative egg chamber expressing RacN17 in border cells and posterior follicle cells (Gal4-306;UAS-RacN17). (F) β-Galactosidase activity staining of a stage 10 egg chamber (Gal4-306;UAS-RacN17; slbo1/+), showing that the cells at the anterior tip are border cells. (G) High power confocal micrograph of stage 10 border cells from Gal4-306;UAS-RacN17 stained for F-actin. Note the lack of cellular extensions of filopodia. (H) Nuclear staining of G. (I) F-actin staining of a stage 9 egg chamber expressing dominant-negative RhoL. (J) β-Galactosidase activity staining in a similar egg chamber. Arrows indicate border cells.
