Picture from Susoy, Vladislav et al. (2019) MicroPubl Biol

Figure 1. Psto3::wrmScarlet reporter is expressed in R4BL/R and R8BL/R ray neurons.

Picture from Etchberger JF et al. (2007) Genes Dev "The molecular signature and cis-regulatory architecture of a C. elegans ...."

The srd-33 7TMR reporter gene fusion also shows a restricted expression pattern (ASEL/R, AWBL/R, ASHL/R, AVKL/R, PHAL/R, PHBL/R, and weakly in another unidentified tail neuron pair, possibly PHCL/R). Each data set of micrographs shows expression of the reporter construct under investigation in a high-magnification (400x) image, the overlap with a red fluorescent marker for ASEL/ASER (otIs151 transgene; 'ASE-RFP'), and a low-magnification (160x) overview of expression of the reporter construct under investigation throughout the whole worm. In the low-magnification images, the asterisk (*) indicates expression of the gut-specific injection marker elt-2::gfp.

Picture from Lin L et al. (2013) J Cell Biol "The scaffold protein EPG-7 links cargo-receptor complexes with the autophagic ...."

At larval stages, W07G4.5::GFP forms aggregates in intestinal cells (Q and R).

Picture from Yan D et al. (2009) Cell "The DLK-1 kinase promotes mRNA stability and local translation in C. elegans ...."

Figure S7. Colocalization analysis of MAK-2 and CEBP-1 with presynapticmarkersAll images are of synaptic regions of the dorsal processes of GABAergic motorneurons. For each panel, pixel values obtained from line scans of a confocalprojection (on left) are plotted on the right. Pearson's correlation coefficient r and the probability were calculated. (A) mCherry::MAK-2 (juEx1503) partly colocalizes with SNB-1::GFP (juIs1). r = 0.69, P < 0.0001. (B) In rpm-1(lf) mutants mCherry::MAK-2 and SNB-1::GFP are aberrantly distributed but remain colocalized. (C) mCherry::MAK-2 does not colocalize with RPM-1::GFP (juIs77). r = -0.14, P = 0.054. (D) mCherry::CEBP-1 (juEx1735) colocalizes with SNB1::GFP. r = 0.88, P < 0.0001.(E) mCherry::CEBP-1 is excluded from areas of RPM-1::GFP. r = -0.67, P < 0.001. (F) mCherry::MAK-2 and CEBP-1::GFP (juEx2157) partly colocalize; r = 0.48, P < 0.0001. Scale, 10 um.

Picture from Mariner BL et al. (2023) MicroPubl Biol "Easy C. elegans Worm Lifespan Plotting and Statistics with ...."

Figure 1. Example plot generated from WLSplot workflow:Visualization of WLS_autoplot() features when plotting worm lifespan data with the WLSplot R package.

Picture from Etchberger JF et al. (2007) Genes Dev "The molecular signature and cis-regulatory architecture of a C. elegans ...."

Figure 2. Expression patterns of genes from the SAGE library as assessed by gfp reporter gene technology. Only a selected and representative number of examples are shown in this figure. All analyzed reporter strains, including those shown here, are shown in Supplementary Figures 1-3. Green boxes indicate gfp coding sequences (rfp in the case of dop-3 and yfp in the case of hlh-10). If extrachromosomal arrays were generated, multiple lines were analyzed for each reporter construct, as indicated below each panel of micrographs. Each data set of micrographs shows expression of the reporter construct under investigation in a high-magnification (400x) image, the overlap with a red fluorescent marker for ASEL/ASER (otIs151 transgene; 'ASE-RFP'), and a low-magnification (160x) overview of expression of the reporter construct under investigation throughout the whole worm. In the low-magnification images, the asterisk (*) indicates expression of the gut-specific injection marker elt-2::gfp. (A) Expression patterns of two selected TFs from the SAGE data set. (B) Expression patterns of two selected peptidergic signaling proteins from the SAGE data set. (C) Expression patterns of two selected putative chemoreceptor proteins of the 7TMR family from the SAGE data set. The srg-30 7TMR-type chemoreceptor shows the most restricted expression pattern with strong expression in ASEL/R and weak expression in the chemosensory neurons ASIL/R and ADLL/R. Additional expression can be observed in a pharyngeal neuron. The srd-33 7TMR reporter gene fusion also shows a restricted expression pattern (ASEL/R, AWBL/R, ASHL/R, AVKL/R, PHAL/R, PHBL/R, and weakly in another unidentified tail neuron pair, possibly PHCL/R). The bottom panels in C demonstrate that 7TMR-type chemoreceptors localize to the dendritic ending of the ASE neurons. In order to boost expression in the ASE neurons, a 188-bp ASEL-specific regulatory element from the gcy-7 gene was appended to each locus (indicated as a black box). One transgenic line each was analyzed in detail. Yellow arrows point to the dendritic endings.

Picture from Lu Q et al. (2011) Dev Cell "The WD40 repeat PtdIns(3)P-binding protein EPG-6 regulates progression of ...."

Q-T. Expression of gfp::epg-6 in the head region (Q), body wall muscles (R), the tail region (S) and the ventral cord (T) at larval stages.

Picture from Etchberger JF et al. (2007) Genes Dev "The molecular signature and cis-regulatory architecture of a C. elegans ...."

The srg-30 7TMR-type chemoreceptor shows the most restricted expression pattern with strong expression in ASEL/R and weak expression in the chemosensory neurons ASIL/R and ADLL/R. Additional expression can be observed in a pharyngeal neuron. Each data set of micrographs shows expression of the reporter construct under investigation in a high-magnification (400x) image, the overlap with a red fluorescent marker for ASEL/ASER (otIs151 transgene; 'ASE-RFP'), and a low-magnification (160x) overview of expression of the reporter construct under investigation throughout the whole worm. In the low-magnification images, the asterisk (*) indicates expression of the gut-specific injection marker elt-2::gfp.

Picture from Li M et al. (2005) Dev Cell "Regulatory mutations of mir-48, a C. elegans let-7 family MicroRNA, cause ...."

(P-R) mir-241::gfp is expressed in a variety of cell types as indicated for the (P) L3 and (R) L2 stages. (Q) is the Nomarski DIC image corresponding to (P). The bar in (B) is 10 um and applies to all panels except (J) and (O); the bar in (J) is 20 um. Stage-nonspecific expression was observed in unidentified neurons in the head, tail, and ventral nerve cord.

Picture from Huang X et al. (2004) Development "The AHR-1 aryl hydrocarbon receptor and its co-factor the AHA-1 aryl hydrocarbon ...."

Figure 4. AHR-1 is expressed in RMEL/R cells. (A) Nomarski picture of the head of an animal, with an enlarged view shown in B. (C) Fluorescence image of Pahr-1GFP expression. Overlay is shown D. Arrows indicate the RMEL neurons. Pahr-1GFP is also brightly expressed in a pair of sensory neurons (arrowhead), likely to be ASKL/R. Scale bar: in A,C,D, 50 um; in B, 20 um.