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Expr15619
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Expr15558
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Expr15567
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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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Expr12196
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To determine where lite-1 is expressed and identify likely sites of lite-1 function, the authors generated and examined worms carrying one of four transgenes derived from the wild-type lite-1 locus: a genomic fragment (lite-1 genomic), a transcriptional fusion (lite-1prom::gfp), a C-terminal translational fusion (lite-1prom::lite-1::gfp), and an N-terminal translational fusion (lite-1prom::gfp::lite-1). GFP expression was observed in a total of 29 cells: pharyngeal neurons M1, M4, M5, and MI; non-pharyngeal neurons ASK, ADL, ASI, ASH, AVG, AVB, RIM, ADF, PHA, PHB, and PVT; and non-neuronal cells Hyp3 (hypoderm), AMso (amphid socket cells), and PHso (phasmid socket cells). AVB was observed only with the C-terminal fusion transgene, and RIM and ADF were observed only with the transcriptional fusion transgene. lite-1 expression in AVG and PVT was previously reported. |
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Expr15598
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Picture: Fig 3. |
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Expr8850
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Neuronal Expression: AVA, AVB, AVE, PVC, AIB, AUA, AVG, RIB, RIC, SAA, SIA, SIB, RIF, RIM, RMD, RME, SMD, DA, DB, VA, VB, M5, NSM, MC, I3, MI?. Non-neuronal Expression: rectal epithelium, body wall muscle, spermethecae, vulva muscle. |
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Expr15604
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Expr15608
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Expr15611
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Expr249
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AVG AVJ DVC PVC PVQ RIG RIS RMD RMEL/R SMD URY [Nature 378:82] |
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Expr14671
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The lin-11-int3p::GFP (pGLC59) transgenic lines that contain the entire intron 3 sequence showed GFP reporter expression in seven neurons at the larval stage L4. These include two sensory neurons (ADL and ADF), four interneurons (AVJ, RIC, AIZ, and RIF) and one pioneer interneuron (AVG). Expression was also detected in embryos. Because some of the lin-11 neurons are specified in the embryo, lin-11::GFP was expected to be expressed in these neurons during their specification. Consistent with this, GFP fluorescence was observed as early as in the pre-gastrula stage in the presumptive head and tail regions. By the 3-fold embryonic stage, fluorescence could be seen in neuronal cells in the anterior region. GFP fluorescence in ADL, ADF and AVJ was very strong and observed in almost all animals. Fluorescence was less frequently observed in RIC and AIZ and was rarely seen in RIF and AVG. |
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Expr14672
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Intron 7-driven GFP reporter fluorescence was first detected in two head neurons in post-gastrulating embryos; based on reporter gene expression, one of those neurons is likely to be AVG. The identification of this neuron as AVG in larval stages was confirmed by co-localization with two reporters, glr-1::DsRed and odr-2::DsRed (Chou et al., 2001; Maricq et al., 1995). The other unidentified cell had variable fluorescence. Fluorescence in lin-11-int-7p::GFP animals persisted in both neurons throughout the larval stages, but the intensity decreased with time. Adults showed faint expression mostly in AVG. |
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Expr12087
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GFP expression is detectable in comma stage embryos with strongest expression in the tail region. The distinct subcellular localization makes it difficult to confirm cell identities, but overall expression is comparable to the plr-1::GFP promoter construct. Postembryonical GFP expression in the head region seems restricted to some neurons and the posterior region of the pharynx. Expression was not readily detectable in hypodermal or body wall muscle cells with this construct postembryonically. Expression of the PLR-1::GFP fusion protein, however, is detectable in the AVG neuron and also in the excretory cell. This suggests that the promoter construct lacks some control elements. Since the GFP expression of the fusion protein is significantly lower than the expression of the promoter construct, it is possible that low levels of expression in tissues and cells expressing the plr-1::GFP transcriptional reporter remain undetectable. |
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Expr14117
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Several head sensory neurons (ASI, ASH, ASJ), one neuron pair in ventral ganglion, AVG, ALN, PLN, pharynx |
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Clone: pUL#JRH/AH7 |
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Expr7632
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Expression is seen in 2 nerve cells in the head and 5 in the tail. The expression is very specific, late embryo to adult. Expressing nerve cells may be AVG, M5, PVT and 4 of PVCL/R, PVNL/R, PVQL/R. |
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Expr9959
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PDF-2::GFP signals could be observed throughout post-embryonic life. The PDF-2::GFP-expressing cells were identified as the interneurons BDUL/R, AVG, AIML/R, RIS, AVD and PVT, the chemosensory neuron pairs PHA and PHB, the motor neurons RID and RIML/R, the sensory neurons AQR and PQR, and less frequently in the PVPL/R interneurons. Outside the nervous system, strong expression was observed in rectal gland cells rectD and rectVL/R, the intestino-rectal valve cells virL/R and three posterior arcade cells in the head. Weak GFP fluorescence could also be observed in four additional head neurons that could not be unequivocally identified. GFP fluorescence was visible in neuronal cell bodies, axons and dendrites. |
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Expr15648
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Picture: Fig 6. |
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Expr8786
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Apart from cells in the neuroblast lineage that generate ASE, nhr-67::mCherry was expressed in multiple other neuroblast lineages in the developing embryo. Expression was usually observed in the grandmother or mother of a neuron, but not earlier. Within the ASEL and ASER-generating lineage branches, nhr-67 was expressed in neuroblasts that generate closely or distantly related cousins of ASEL and ASER. For example, the sister neuroblast of the ASE-generating neuroblast creates the AUA and ASJ neurons and it expressed nhr-67. The cousin of the ASE-mother cell generates the AWB and ADF sensory neurons. nhr-67 was expressed in these cells. In late stage embryos, a few other, postmitotic neurons started to express nhr-67. Embryonic nhr-67 expression was not restricted to the nervous system, but was observed in a small subset of mesodermal and hypodermal cells. No expression was detected in endodermal cells or the germ line. nhr-67 was expressed in the excretory canal cell. Postembryonically, nhr-67 expression persisted only in a few neurons in the head ganglia until the first larval stage and faded shortly thereafter in most, but not all, of these neurons, with expression persisting through adulthood only in the CEPD/V, RMED/V, AVL and RIS neurons. During mid-larval development, nhr-67 was transiently and dynamically expressed in the AC cells of the vulva. Expression was also found in the VU cells and somatic gonad, but not in vulA, vulB or vulC. Within the ASEL/R generating lineages, nhr-67::mCherry was first observed in the grandmother cells of ASEL and ASER. Transgenic animals that co-express a functional nhr-67::mCherry reporter and a functional che-1::yfp reporter revealed that nhr-67 precedes che-1 expression. nhr-67 expression was maintained in the ASEL and ASER neurons until the first larval stage after which it became undetectable, whereas che-1 expression was maintained throughout the life of the animal. In spite of its genetically deduced role in asymmetric gene expression in ASEL and ASER, nhr-67 expression is bilaterally symmetric in ASEL and ASER. |
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Expr12717
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At 335 minutes post fertilization. |
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Expr11224
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efn-2 expression showed widespread left-right asymmetry inembryos, both in amphid neurons and in other cells. |
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