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Expr4382
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Expressed in AVA, RIB, RID, SIB, SMD, CEP(?), ADE(?), some unidentified neurons in the head and tail. Also expressed in anal depressor, head muscles (strong), body wall muscles (strong). |
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sin-3 = pqn-28 according to this paper. |
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Expr4679
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When the sin-3 expression profile was examined in transgenic animals using a gfp reporter driven by a 1.5 kb sin-3 5'-flanking sequence, the sin-3::gfp signal was detected in all the ray structural cells. In addition, sin-3::gfp expression was observed in the inner labial neurons, socket cells, the cephalic neurons in the head region and the ventral nerve cord from L1 to adult stage. |
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Expr16352
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We confirmed previous reports that the asic-1 promoter drives expression in the ADE, CEP, PVQ, PDE and PVD neurons (De Stasio et al., 2018; Husson et al., 2012; Voglis & Tavernarakis, 2008) and also observed expression in FLP and ventral cord neurons. |
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Expr11820
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asic-1 is expressed in eight neurons comprising the C. elegans dopaminergic system (the four cephalic neurons; two anterior deirid neurons and two posterior deirid neurons; CEP, ADE, PDE, respectively). Expression is also detected in four additional neurons in the tail, two of which are the bilaterally symmetric PVQ interneurons. |
A full-length ASIC-1::GFP and an amino-terminal ASIC-1N::GFP chimaeras showed prominent punctuate distribution along the processes of dopaminergic neurons, in synapse-rich areas. A DsRED-synaptobrevin fusion colocalizes with both ASIC- 1::GFP and ASIC-1N::GFP in these puncta. Thus, ASIC-1 localizes at presynaptic termini of dopaminergic neurons. |
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Expr15649
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Picture: Figure 2B. Reporter gene fusion type not specified. |
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Marker31
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Expressed in CEP neurons. |
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Expr11574
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atat-2 is expressed not only in touch receptor neurons but also in a subset of ciliated neurons, namely, PDE, ADE, CEP, and OLQ. |
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Expr14514
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Full-length NPHP-2::GFP localized to a short proximal region of amphid channel and phasmid cilia as well as IL, CEP, OLQ, amphid channel and phasmid cilia, and the AWC wing cilia. Native promoter driven NPHP-2::GFP was not visible in AWB cilia, as reported previously for AWB- specific promoter driven NPHP-2. We conclude that NPHP-2 marks a region of the cilium distinct from the doublet region, and propose that this region is analogous to the InvC of mammalian cilia. |
genomic |
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Expr11753
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Isoform 1a |
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Expr11754
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Isoform 1b.1 |
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Expr11755
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Expr12168
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qdpr-1 was expressed in the epidermis -similar to what observed in cat-4 transgenics- but was not highly expressed in 5HT and DA neurons. These transgenics all also showed some expression of varying intensity in other cells (non-epidermal cells, and non-5HT and non-DA neurons in the head and body). A qdpr-1 full-length translational fusion was expressed in several known 5HT and DA neurons, including NSMs, ADFs, CEPs, and other cells. |
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Expr15558
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Expr15560
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Expr9325
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Synaptogyrin is expressed in all 26 GABAergic neurons including also RMER and most though not all other neurons. Synaptogyrin is absent in amphids and phasmids and can be detected in non-neuronal glial-like sheath cells in adult worms. The cephalic neurons CEPDR/L and CEPVR/L and amphid-associated sheath cells CEPshDR/L, CEPshVR/L were tentatively positive. Several other neurons that could be tentatively identified in the anterior part are MI, M4, I4, AVL, AIY, RIS, I5, M3R/L, and in the posterior part DVA, AS11, ALNR/L, DVC, DVB, PQR, DA9 (characteristic axonal process denoted by arrowhead), VD13, DD6, VD12. Of these, AVL, RIS, VD13, DD6 and VD12 are GABAergic based on the colocalization with the unc-47p::GFP reporter. In addition, IL neurons were tentatively identified in the anterior (IL*). Synaptogyrin reporter constructs are also expressed in developing neurons. The expression of sng-1p::YFP is closely associated with the development of the nervous system being absent in the gastrula stage with first fluorescence in neuronal precursor cells and newly-formed neurons in the anterior part during the 1.5-fold stage. In addition, it is also detected transiently in cells in the posterior body at the 1.25-fold and 1.5-fold stage. |
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Expr15571
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Expr15572
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Expr15573
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Expr15579
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Expr15586
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Expr15651
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Expr15652
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Expr15589
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Expr13158
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Expr15591
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Expr15598
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Expr15604
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Expr14590
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Embryonic expression of exc-7 was first observed at the bean stage. By reverse lineaging with use of SIMI-Biocell software, we confirm the identity of one of the expressing cells at this stage as the excretory canal cell. In L1 animals, broad expression in the head, ventral nerve cord (VNC), and tail was observed. In young adults, expression is notably observed in vulva cells. In the nervous system specifically, expression is observed in many neurons throughout the body, but unlike Drosophila Elav, exc-7::gfp it is not panneuronally expressed. We confirmed previously reported expression in cholinergic VNC MNs, but absence of GABAergic VNC MNs, consistent with previous reports (Fujita et al., 1999; Loria et al., 2003) and consistent with exc-7 functioning in cholinergic, but not GABAergic neurons to control alternative splicing (Norris et al., 2014). exc-7::gfp is also expressed in some non-neuronal cell types, including muscle and hypodermis, but not in the gut. A previous report showed that exc-7 is only transiently and weakly expressed in the excretory cell, which, based on exc-7's excretory mutant phenotype, has puzzled researchers (Fujita et al., 2003). We find that the gfp tagged exc-7 locus is strongly and continuously expressed in the excretory canal cell. |
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Expr15608
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Expr15611
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