IMAGE

Fig. 4

ID
ZDB-IMAGE-130426-8
Genes
Antibodies
Source
Figures for Choe et al., 2013
Image
Figure Caption

Fig. 4 Wnt Signaling and Cdc42 Regulate Junctional Localization of Alcama in Developing Pouches(A–D) Immunohistochemistry shows progressive junctional localization of Alcama in the wild-type fourth pouch. Below each image, the normalized intensity of fluorescent signal is plotted along the 35 μM red lines. Asterisks indicate clear cell-cell boundaries.(E–H) Still images from a time-lapse confocal recording of fourth pouch development in nkx2.3:Alcama-GFP; her5:mCherryCAAX transgenic embryos (see Movie S6). As with endogenous Alcama protein, plots of fluorescence intensity through the red lines show progressive junctional localization of Alcama-GFP (green) within her5:mCherryCAAX-positive pouch cells (red).(I–X) Immunohistochemistry shows Alcama localization at the level of the fourth pouch in wild-type, mutant, and fzd8a-MO embryos, as well as UAS transgenic embryos (capitalized) doubly positive for nkx2.3:Gal4VP16. Alcama is partially mislocalized from pouch cell membranes to the cytoplasm in wnt4a-, wnt11r-wnt4a-, and fzd8a-MO embryos but not in wnt11r- embryos. In contrast, misexpression of Wnt11r results in disorganized endoderm (n = 28/32, data not shown) and occasionally rosette-like structures (n = 3/32), with rosette-like structures never observed in fzd8a-MO-injected siblings (n = 0/23, p = 0.003). Similarly, the inappropriate Alcama junctional localization induced by Wnt4a misexpression (n = 26/114) was never seen in fzd8a-MO-injected siblings (n = 0/74, p = 0.004) or doubly transgenic Wnt4a; DN-Cdc42 embryos (n = 0/31, p = 0.005). Rosette-like structures were observed in both CA-Rac1 embryos (n = 104/112) and their wnt11r mutant siblings (n = 11/17), and hyperelongated pouches were observed in both CA-Cdc42 embryos (n = 85/122) and their wnt4a-MO-injected siblings (n = 72/101). Plots of fluorescence intensity through the red lines are shown, with asterisks indicating clear cell-cell junctions.(Y–AB) Immunohistochemistry and normalized line plots show junctional localization of E-cadherin throughout wild-type pouch development, with pronounced apical enrichment (arrow in AA) as pouches mature. Inhibition of Dvl in nkx2.3:Gal4VP16; UAS:DvlΔDEP embryos does not significantly disrupt E-cadherin localization.See also Figure S3.

Figure Data
Acknowledgments
This image is the copyrighted work of the attributed author or publisher, and ZFIN has permission only to display this image to its users. Additional permissions should be obtained from the applicable author or publisher of the image.

Reprinted from Developmental Cell, 24(3), Choe, C.P., Collazo, A., Trinh, L.A., Pan, L., Moens, C.B., and Crump, J.G., Wnt-Dependent Epithelial Transitions Drive Pharyngeal Pouch Formation, 296-309, Copyright (2013) with permission from Elsevier. Full text @ Dev. Cell