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Expr4403
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Strong and consistent expression was observed in a limited number of neurons in the head and tail and coelomocytes. Weaker and/or inconsistent expression of TTX-7::EGFP was detected in nerve cord motor neurons, intestine, and somatic gonad. The head neurons expressing ttx-7::EGFP include AFD and RIA neurons. Also expressed in ASH, ASE, ASJ, AWC, ADF, ADL, ASI, ASK, AWB, VNC motor neurons, etc. |
TTX-7::EGFP was diffusely expressed in the cytoplasm and was not localized to any specific subcellular compartment. |
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Expr4526
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Expressed in AWAL/R, ASIL/R, RIAL/R, PVT. |
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Expr15388
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Expr15558
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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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Expr15608
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Expr11375
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eat-4 is expressed in 78 of the 302 neurons of the adult hermaphrodite, which fall into 38 neuron classes (out of a total of 118 anatomically defined neuron classes in the hermaphrodite). Most of these neurons are either sensory- or interneurons. Only two motorneurons utilize glutamate; both are located in the pharynx. |
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Expr15611
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Cells expressing TAX-6 were visualized using several tax-6::gfp fusion genes. The expression of tax-6 is under diverse transcriptional controls. Reporter gene fusion type not specified. pAK43 is a larger transgene that should include all promoter regions for tax-6 transcription, since another gene is encoded just upstream of this region and tax-6 mRNA does not seem to be derived from a polycistronic transcript. |
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Expr1824
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When introduced into wildtype animals, pAK43 drove TAX-6 expression in many sensory neurons, as well as interneurons including AIY and AIZ, and most, if not all, muscle cells. pAK43 is expressed in muscle, AIB, AIY, AIZ, RIA, RIB, RIS, RIM, ASI, ADF, ASH, ASK, ADL, AUA, PHA, PHB, AVE. It is also expressed in AFD, ASE, AWA, AWC, AVK, AIM, RMDV, AVA. |
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Expr12599
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Broad expression of the frpr-4::gfp translational reporter was observed during both larval development and adulthood; expression was in body wall muscles, pharyngeal muscles, and multiple neurons, including the RIA neurons, the DVA neuron, and the PVM neuron. Membrane localization of the green fluorescence was observed, as would be expected for a GPCR. |
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Picture: Fig. 7. |
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Expr7825
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The most predominant fluorescence was detected in the head ganglia and the ring neuropile. Among the head neurons labeled, strong and consistent fluorescence was detected in the bilaterally symmetrical pair of RIA interneurons and, less strongly but also consistently, in the bilaterally symmetrical RIC neurons. In addition, inconsistent staining of URY was detected. Outside the head region consistent labeling of the tail neuron, PVT, and possibly DVC was detected, although this latter neuron could not be positively identified. Authors could not detect any consistent expression of our ser-1::GFP construct in muscle either of the body wall, vulva or pharynx. |
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Expr15344
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[ser-2::gfp] transcriptional fusion constructs. Ser-2 reporter constructs were generated by using a PCR fusion protocol, using pPD95.75 as a template for green fluorescent protein (gfp). For all gfp fusion primers listed, gfp vector sequence is indicated in lowercase, and gene-specific sequence is indicated in uppercase. [ser-2::gfp] translational fusion. A translational fusion of the whole ser-2 locus to gfp was created by using an in vivo recombination technique. Specifically, two overlapping PCR fragments, one containing the 5' part of a locus, the other containing the remainder of the locus PCR-fused to gfp, were coinjected into the worm. Recombination of these two fragments via the homologous region leads to the expression of a full-length ser-2::gfp fusion. |
Expr2707
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Expression using the upstream regulatory regions of exon 1bc (ser-2prom2::gfp) is mostly restricted to the AIYL/R, AIZL/R, RID, DVA, BDUL/R, SIADL/R, and SIAVL/R interneurons. Less consistent expression is observed in PVT. In addition, expression is observed in the RMEL/R motor neurons. Outside the nervous system, expression can be observed in the excretory gland cells. No more transcriptional regulatory information is contained within intronic regions by generating a fusion of gfp to the full coding genomic ser-2 locus using an in vivo recombination technique([ser-2::gfp] translational fusion. Transgenic animals expressing such a construct show an expression pattern similar to the one observed with the ser-2prom1::gfp construct. The upstream regulatory region of the third splice form, containing exon 1d(ser-2prom3::gfp), drives expression exclusively in two sensory neuron classes, OLL(L/R) and PVD(L/R). ser-2prom1::gfp is expressed in the AIY interneuron class and a set of unidentified neurons. These neurons were identified as head and tail interneuron classes, namely AVHL/R, AUAL/R, AIYL/R, RICL/R, SABVL/R, RID, RIAL/R, SABD, SDQ, CANL/R, DA9, LUAL/R, ALNL/R, and PVCL/R. In addition to its expression in neurons, ser-2prom1::gfp is also expressed in pharyngeal cells (NSM neurons and pm1/6 muscles) and in head muscles. In males, expression can be observed in posterior dorsal and ventral body wall muscles, the male-specific diagonal muscles, and several posterior neurons likely to be CP neurons. |
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Picture: Fig. 2a, b. |
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Expr8733
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MAGI-1::GFP was expressed in several interneurons, including AVA, AVD, AVE, RIM, and RIA. |
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Expr15570
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Expr3206
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In addition to expression in a number of neurons (RMEL/R, RID, BDUL/R, AIYL/R, AVHL/R, AIZL/R, ALNL/R, RICL/R, RIAL/R and PDA) as has been reported previously, intense fluorescence was also observed in uterine toroid cells (ut1 and ut2). |
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Expr15648
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Expr15626
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Promoter 6-1 |
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Expr15340
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