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. Author manuscript; available in PMC: 2010 Mar 1.
Published in final edited form as: Nat Genet. 2009 Aug 16;41(9):1022–1026. doi: 10.1038/ng.425

Figure 4. Consequences of SHOC2S2G expression in C. elegans vulva development.

Figure 4

(a–d) Nomarski images of vulvas of adult animals. A normal vulva is observed in animals expressing SHOC2wt (a), while in worms expressing SHOC2S2G (b and c) or myr::SHOC2wt (d) a protrusion of the vulva is visible. (e–j) Subcellular localization of V5-tagged SHOC2 proteins in C. elegans cells. In excretory canal cells (e–g) and intestinal cells (h–j), SHOC2wt protein is present throughout the cytoplasm (e and h), while both SHOC2S2G (f and i) and myr::SHOC2wt (g and j) are enriched in or restricted to the plasma membrane. Anti-V5 antibody (red) was used to visualize SHOC2 proteins. In intestinal cells, nuclei express GFP due to pelt-2::GFP plasmid used as a marker for transformation. (k–n) Nomarski images of vulval precursor cells at L3 stage. In animals expressing SHOC2wt only P6.p descendant invaginate (k), while in SHOC2S2G (l and m) and myr::SHOC2wt (n) expressing animals also P5.p (l to n) and P7.p descendants (m and n) detach from the cuticle. Black arrowheads point to P6.p descendant invagination, while white arrowheads point to P5.p and P7.p descendant invagination. Anterior is to the left and dorsal is up in all images.