spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


Right arrow Help viewing high resolution images
Right arrow Return to article
(Downloading may take up to 30 seconds.
If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.


Figure 5


Fig. 5. EGL-43 is involved in AC invasion as a downstream target of HLH-2 and FOS-1. Animals containing cdh-3::CFP (red) were injected with egl-43 (PR-domain)::YFP constructs. (A-F) The PR-YFP transgene is expressed (green) in the VU and DU lineages as well as in the AC from early L2 when using the wild-type egl-43 regulatory region (A,B), and shows the AC (cdh-3::CFP, white) invasion defect (E). The transgene is expressed in the VU and DU lineages from late L2, but in the AC from mid-L3, when using the mutated E-boxes (C,D), and shows normal AC invasion (F). (G-L) egl-43 RNAi eliminates expression of zmp-1::GFP (G,H) and him-4::GFP (I,J) in the AC (arrow), but not of fos-1::YFP (K,L). egl-43 RNAi resulted in two ACs in which fos-1::YFP is expressed higher than in the neighboring gonadal cells (L, arrows). (M-R) fos-1 RNAi greatly reduces egl-43 expression in the AC, and in the DU and VU descendants at the L3 molt (M,N) and at mid-L3 (Q,R), but not at mid-L2 (O,P). Animals from a transgenic line that expresses egl-43(exon-5)::YFP were used for the fos-1 RNAi.





Right arrow Return to article