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Loss of pseudouridine synthases in the RluA family causes hypersensitive nociception in Drosophila
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/dvdy.22737openalex-snapshot
Pokes, sunburn, and hot sauce: Drosophila as an emerging model for the biology of nociception
inferredcites →https://doi.org/10.1007/978-1-60327-323-7_2openalex-snapshot
Alternatives to Mammalian Pain Models 2: Using Drosophila to Identify Novel Genes Involved in Nociception
inferredcites →https://doi.org/10.1007/s004380050866openalex-snapshot
The Nop60B gene of Drosophila encodes an essential nucleolar protein that functions in yeast
inferredcites →https://doi.org/10.1016/j.ajhg.2018.10.026openalex-snapshot
Variants in PUS7 Cause Intellectual Disability with Speech Delay, Microcephaly, Short Stature, and Aggressive Behavior
inferredcites →https://doi.org/10.1016/j.cell.2010.09.047openalex-snapshot
A Genome-wide Drosophila Screen for Heat Nociception Identifies α2δ3 as an Evolutionarily Conserved Pain Gene
inferredcites →https://doi.org/10.1016/j.cell.2014.08.028openalex-snapshot
Transcriptome-wide Mapping Reveals Widespread Dynamic-Regulated Pseudouridylation of ncRNA and mRNA
inferredcites →https://doi.org/10.1016/j.celrep.2011.11.002openalex-snapshot
Thermosensory and Nonthermosensory Isoforms of Drosophila melanogaster TRPA1 Reveal Heat-Sensor Domains of a ThermoTRP Channel
inferredcites →https://doi.org/10.1016/j.celrep.2014.10.034openalex-snapshot
Identification of Ppk26, a DEG/ENaC Channel Functioning with Ppk1 in a Mutually Dependent Manner to Guide Locomotion Behavior in Drosophila
inferredcites →https://doi.org/10.1016/j.celrep.2015.01.059openalex-snapshot
Plug-and-Play Genetic Access to Drosophila Cell Types using Exchangeable Exon Cassettes
inferredcites →https://doi.org/10.1016/j.celrep.2016.06.003openalex-snapshot
Nociceptor-Enriched Genes Required for Normal Thermal Nociception
inferredcites →https://doi.org/10.1016/j.celrep.2017.09.001openalex-snapshot
Enclosure of Dendrites by Epidermal Cells Restricts Branching and Permits Coordinated Development of Spatially Overlapping Sensory Neurons
inferredcites →https://doi.org/10.1016/j.celrep.2018.08.070openalex-snapshot
The Drosophila Small Conductance Calcium-Activated Potassium Channel Negatively Regulates Nociception
inferredcites →https://doi.org/10.1016/j.chembiol.2006.09.009openalex-snapshot
Pseudouridine Synthases
inferredcites →https://doi.org/10.1016/j.conb.2017.05.005openalex-snapshot
mRNA transport & local translation in neurons
inferredcites →https://doi.org/10.1016/j.cub.2004.01.052openalex-snapshot
nanos and pumilio Are Essential for Dendrite Morphogenesis in Drosophila Peripheral Neurons
inferredcites →https://doi.org/10.1016/j.cub.2004.09.085openalex-snapshot
The Drosophila Fragile X Gene Negatively Regulates Neuronal Elaboration and Synaptic Differentiation
inferredcites →https://doi.org/10.1016/j.cub.2007.11.029openalex-snapshot
Nociceptive Neurons Protect Drosophila Larvae from Parasitoid Wasps
inferredcites →https://doi.org/10.1016/j.cub.2008.04.033openalex-snapshot
Spatial Regulation of nanos Is Required for Its Function in Dendrite Morphogenesis
inferredcites →https://doi.org/10.1016/j.cub.2009.12.057openalex-snapshot
Pickpocket Is a DEG/ENaC Protein Required for Mechanical Nociception in Drosophila Larvae
inferredcites →https://doi.org/10.1016/j.cub.2010.07.016openalex-snapshot
Bicaudal-D Regulates Fragile X Mental Retardation Protein Levels, Motility, and Function during Neuronal Morphogenesis
inferredcites →https://doi.org/10.1016/j.cub.2012.09.019openalex-snapshot
Dendritic Filopodia, Ripped Pocket, NOMPC, and NMDARs Contribute to the Sense of Touch in Drosophila Larvae
inferredcites →https://doi.org/10.1016/j.cub.2014.10.038openalex-snapshot
Balboa Binds to Pickpocket In Vivo and Is Required for Mechanical Nociception in Drosophila Larvae
inferredcites →https://doi.org/10.1016/j.cub.2016.09.038openalex-snapshot
The TRP Channels Pkd2, NompC, and Trpm Act in Cold-Sensing Neurons to Mediate Unique Aversive Behaviors to Noxious Cold in Drosophila
inferredcites →https://doi.org/10.1016/j.cub.2017.07.031openalex-snapshot
Nociceptive Circuits: Can’t Escape Detection
inferredcites →https://doi.org/10.1016/j.jpain.2012.03.009openalex-snapshot
The Economic Costs of Pain in the United States
inferredcites →https://doi.org/10.1016/j.molcel.2006.09.017openalex-snapshot
Crystal Structure of Pseudouridine Synthase RluA: Indirect Sequence Readout through Protein-Induced RNA Structure
inferredcites →https://doi.org/10.1016/j.neuron.2011.10.036openalex-snapshot
Integrins Regulate Repulsion-Mediated Dendritic Patterning of Drosophila Sensory Neurons by Restricting Dendrites in a 2D Space
inferredcites →https://doi.org/10.1016/j.neuron.2016.01.020openalex-snapshot
Epidermis-Derived Semaphorin Promotes Dendrite Self-Avoidance by Regulating Dendrite-Substrate Adhesion in Drosophila Sensory Neurons
inferredcites →https://doi.org/10.1016/j.tibs.2013.01.002openalex-snapshot
RNA pseudouridylation: new insights into an old modification
inferredcites →https://doi.org/10.1016/j.ymeth.2013.12.002openalex-snapshot
Targeted genome engineering techniques in Drosophila
inferredcites →https://doi.org/10.1016/s0092-8674(03)00272-1openalex-snapshot
painless, a Drosophila Gene Essential for Nociception
inferredcites →https://doi.org/10.1016/s0960-9822(03)00596-7openalex-snapshot
Enhanced Locomotion Caused by Loss of the Drosophila DEG/ENaC Protein Pickpocket1
inferredcites →https://doi.org/10.1021/bi00190a008openalex-snapshot
Crystal Structure of Unmodified tRNAGln Complexed with Glutaminyl-tRNA Synthetase and ATP Suggests a Possible Role for Pseudo-Uridines in Stabilization of RNA Structure
inferredcites →https://doi.org/10.1038/mt.2008.200openalex-snapshot
Incorporation of Pseudouridine Into mRNA Yields Superior Nonimmunogenic Vector With Increased Translational Capacity and Biological Stability
inferredcites →https://doi.org/10.1038/nature09576openalex-snapshot
Light-avoidance-mediating photoreceptors tile the Drosophila larval body wall
inferredcites →https://doi.org/10.1038/nature10165openalex-snapshot
Converting nonsense codons into sense codons by targeted pseudouridylation
inferredcites →https://doi.org/10.1038/nature10801openalex-snapshot
The role of Drosophila Piezo in mechanical nociception
inferredcites →https://doi.org/10.1038/nature13802openalex-snapshot
Pseudouridine profiling reveals regulated mRNA pseudouridylation in yeast and human cells
inferredcites →https://doi.org/10.1038/nature14297openalex-snapshot
A multilevel multimodal circuit enhances action selection in Drosophila
inferredcites →https://doi.org/10.1038/nchembio.1836openalex-snapshot
Chemical pulldown reveals dynamic pseudouridylation of the mammalian transcriptome
inferredcites →https://doi.org/10.1038/ng1312openalex-snapshot
Systematic generation of high-resolution deletion coverage of the Drosophila melanogaster genome
inferredcites →https://doi.org/10.1038/nmeth.1331openalex-snapshot
Versatile P[acman] BAC libraries for transgenesis studies in Drosophila melanogaster
inferredcites →https://doi.org/10.1038/nmeth.1662openalex-snapshot
MiMIC: a highly versatile transposon insertion resource for engineering Drosophila melanogaster genes
inferredcites →https://doi.org/10.1038/nn.4580openalex-snapshot
Sensory integration and neuromodulatory feedback facilitate Drosophila mechanonociceptive behavior
inferredcites →https://doi.org/10.1038/nprot.2013.143openalex-snapshot
Genome engineering using the CRISPR-Cas9 system
inferredcites →https://doi.org/10.1038/nsb873openalex-snapshot
Sculpting of the spliceosomal branch site recognition motif by a conserved pseudouridine
inferredcites →https://doi.org/10.1038/s41598-017-00446-8openalex-snapshot
Drosophila dyskerin is required for somatic stem cell homeostasis
inferredcites →https://doi.org/10.1073/pnas.1817334116openalex-snapshot
Transcriptome-wide profiling of multiple RNA modifications simultaneously at single-base resolution
inferredcites →https://doi.org/10.1074/jbc.274.27.18880openalex-snapshot
Functional Effect of Deletion and Mutation of theEscherichia coli Ribosomal RNA and tRNA Pseudouridine Synthase RluA
inferredcites →https://doi.org/10.1083/jcb.144.6.1123openalex-snapshot
minifly, A Drosophila Gene Required for Ribosome Biogenesis
inferredcites →https://doi.org/10.1086/302446openalex-snapshot
X-Linked Dyskeratosis Congenita Is Predominantly Caused by Missense Mutations in the DKC1 Gene
inferredcites →https://doi.org/10.1093/nar/24.12.2411openalex-snapshot
Pseudouridine Synthases: Four Families of Enzymes Containing a Putative Uridine-Binding Motif Also Conserved in dUTPases and dCTP Deaminases
inferredcites →https://doi.org/10.1109/isbi.2016.7493338openalex-snapshot
CRF formulation of active contour population for efficient three-dimensional neurite tracing
inferredcites →https://doi.org/10.1111/j.1399-0004.2012.01941.xopenalex-snapshot
Drosophila as a tool for studying the conserved genetics of pain
inferredcites →https://doi.org/10.1111/ped.12217openalex-snapshot
Pathophysiology and genetic mutations in congenital sideroblastic anemia
inferredcites →https://doi.org/10.1126/sciadv.aaw4099openalex-snapshot
Nerve injury drives a heightened state of vigilance and neuropathic sensitization in Drosophila
inferredcites →https://doi.org/10.1242/dev.014423openalex-snapshot
Molecules and mechanisms of dendrite development in Drosophila
inferredcites →https://doi.org/10.1242/dev.121.9.2923openalex-snapshot
Origin and specification of type II sensory neurons in Drosophila
inferredcites →https://doi.org/10.1242/dev.129.12.2867openalex-snapshot
Tiling of theDrosophilaepidermis by multidendritic sensory neurons
inferredcites →https://doi.org/10.1261/rna.2550105openalex-snapshot
The pseudouridine synthase RluD is required for normal ribosome assembly and function in Escherichia coli
inferredcites →https://doi.org/10.1371/journal.pone.0071706openalex-snapshot
High-Throughput Analysis of Stimulus-Evoked Behaviors in Drosophila Larva Reveals Multiple Modality-Specific Escape Strategies
inferredcites →https://doi.org/10.1371/journal.pone.0095449openalex-snapshot
Evolution of Bacterial Consortia in Spontaneously Started Rye Sourdoughs during Two Months of Daily Propagation
inferredcites →https://doi.org/10.1387/ijdb.103112cwopenalex-snapshot
Spatially controlled expression of the Drosophila pseudouridine synthase RluA-1
inferredcites →https://doi.org/10.1523/eneuro.0076-15.2015openalex-snapshot
Single-Trial Event-Related Potential Correlates of Belief Updating
inferredcites →https://doi.org/10.1523/jneurosci.5864-12.2013openalex-snapshot
Dynein-Dependent Transport ofnanosRNA inDrosophilaSensory Neurons Requires Rumpelstiltskin and the Germ Plasm Organizer Oskar
inferredcites →https://doi.org/10.15252/embr.201744045openalex-snapshot
Local translation in neuronal compartments: how local is local?
inferredcites →https://doi.org/10.1534/g3.113.009795openalex-snapshot
Extensive Use of RNA-Binding Proteins inDrosophilaSensory Neuron Dendrite Morphogenesis
inferredcites →https://doi.org/10.1534/genetics.113.152710openalex-snapshot
Genome Engineering of Drosophila with the CRISPR RNA-Guided Cas9 Nuclease
inferredcites →https://doi.org/10.7554/elife.08469.009openalex-snapshot
Author response: A genetic toolkit for tagging intronic MiMIC containing genes
inferredcites →https://doi.org/10.7554/elife.26016.038openalex-snapshot
Author response: Nociceptive interneurons control modular motor pathways to promote escape behavior in Drosophila
inferredcites →https://doi.org/10.7554/elife.29754.030openalex-snapshot
Author response: Small conductance Ca2+-activated K+ channels induce the firing pause periods during the activation of Drosophila nociceptive neurons
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1101/pdb.prot108125openalex-snapshot
Mechanical Nociception Assay inDrosophilaLarvae
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