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WBPicture0000007891Descriptiondrag-1 is expressed and functions in the same cell types as the Sma/Mab pathway components. (A-L) Images shown are side views with anterior to the left and posterior to the right. drag-1p::gfp (A-D) and sma-6p::rfp (E-H) colocalize in pharyngeal (A,E,I), hypodermal (B,F,J) and intestinal (C,G,K) cells, but do not colocalize in the male tail (D,H,L). I-L are merged images of A-D and E-H, respectively. (M-O) DRAG-1::GFP (M,N) or LIN-12TM::GFP (O; see Fig. 5 for details) localization in pharyngeal (M), hypodermal (N) and intestinal (O) cells, as visualized by anti-GFP antibody staining. Note that the GFP signal (green) is located outside of the nucleus (blue, stained with DAPI), both at the cell surface and inside the cell. Arrow heads, hypodermal cells; arrow, pharynx. (Q-U) The M lineage expression pattern of drag-1 using LIN-12TM::GFP (green; see Fig. 5 for details). Anti-FOZI-1 antibody staining (red) was used to mark M lineage cells from the 4-M to the 12-M stage (S-U). Only one focal plane was shown for the 8-M (T) and 12-M (U) stage worms. DRAG-1::GFP is present from the 1-M to the 4-M stage (O-S), then becomes fainter at the 8-M stage (T) and undetectable after the 8-M stage (U).
NameF4.large_A.jpg
CropCropped_fromWBPicture0000007890
DepictExpr_patternExpr9068
Expr9069
AnatomyWBbt:0003681
WBbt:0005733
WBbt:0005741
WBbt:0005772
AcknowledgmentTemplateWormBase thanks <Journal_URL> for permission to reproduce figures from this article. Please note that this material may be protected by copyright. Reprinted from <Article_URL>. Copyright (<Publication_year>) with permission from <Publisher_URL>.
Publication_year2010
Article_URLDOIid10.1242/dev.051615
Journal_URLDevelopment
Publisher_URLTheCompanyofBiologists
ReferenceWBPaper00036372