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Conserved nuclear receptors controlling a novel trait target fast-evolving genes expressed in a single cell
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9780470015902.a0024603openalex-snapshot
Structure, Function and Evolution of The Nematode Genome
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Complex Small‐Molecule Architectures Regulate Phenotypic Plasticity in a Nematode
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Molecular cloning of a dominant roller mutant and establishment of DNA‐mediated transformation in the nematode Pristionchus pacificus
inferredcites →https://doi.org/10.1002/jmor.20739openalex-snapshot
Three‐dimensional reconstruction of the pharyngeal gland cells in the predatory nematode Pristionchus pacificus
inferredcites →https://doi.org/10.1007/978-1-4939-7015-5_6openalex-snapshot
Predicting Secretory Proteins with SignalP
inferredcites →https://doi.org/10.1007/s00239-014-9651-yopenalex-snapshot
The Same or Not the Same: Lineage-Specific Gene Expansions and Homology Relationships in Multigene Families in Nematodes
inferredcites →https://doi.org/10.1007/s00427-014-0486-8openalex-snapshot
Gene inactivation using the CRISPR/Cas9 system in the nematode Pristionchus pacificus
inferredcites →https://doi.org/10.1016/j.actbio.2013.08.020openalex-snapshot
Structure–function–property–design interplay in biopolymers: Spider silk
inferredcites →https://doi.org/10.1016/j.cell.2013.09.054openalex-snapshot
A Developmental Switch Coupled to the Evolution of Plasticity Acts through a Sulfatase
inferredcites →https://doi.org/10.1016/j.cell.2014.03.012openalex-snapshot
Nuclear Receptors, RXR, and the Big Bang
inferredcites →https://doi.org/10.1016/j.celrep.2017.09.077openalex-snapshot
Single-Molecule Sequencing Reveals the Chromosome-Scale Genomic Architecture of the Nematode Model Organism Pristionchus pacificus
inferredcites →https://doi.org/10.1016/j.celrep.2018.05.008openalex-snapshot
A Developmental Switch Generating Phenotypic Plasticity Is Part of a Conserved Multi-gene Locus
inferredcites →https://doi.org/10.1016/j.celrep.2018.12.064openalex-snapshot
A Persistence Detector for Metabolic Network Rewiring in an Animal
inferredcites →https://doi.org/10.1016/j.cois.2015.12.003openalex-snapshot
Molecular mechanisms of phenotypic plasticity in social insects
inferredcites →https://doi.org/10.1016/j.cub.2009.01.015openalex-snapshot
Transcriptional autoregulation in development
inferredcites →https://doi.org/10.1016/j.cub.2015.04.017openalex-snapshot
Transcriptional Regulation via Nuclear Receptor Crosstalk Required for the Drosophila Circadian Clock
inferredcites →https://doi.org/10.1016/j.cub.2016.06.018openalex-snapshot
The Nuclear Hormone Receptor NHR-40 Acts Downstream of the Sulfatase EUD-1 as Part of a Developmental Plasticity Switch in Pristionchus
inferredcites →https://doi.org/10.1016/j.cub.2018.06.075openalex-snapshot
The Genetic Basis of Adaptation following Plastic Changes in Coloration in a Novel Environment
inferredcites →https://doi.org/10.1016/j.gde.2017.07.015openalex-snapshot
Decoding the architecture and origins of mechanisms for developmental polyphenism
inferredcites →https://doi.org/10.1016/j.ijpara.2012.05.005openalex-snapshot
The importance of being regular: Caenorhabditis elegans and Pristionchus pacificus defecation mutants are hypersusceptible to bacterial pathogens
inferredcites →https://doi.org/10.1016/j.isci.2018.11.027openalex-snapshot
Adult Influence on Juvenile Phenotypes by Stage-Specific Pheromone Production
inferredcites →https://doi.org/10.1016/j.mod.2006.06.006openalex-snapshot
NHR-40, a Caenorhabditis elegans supplementary nuclear receptor, regulates embryonic and early larval development
inferredcites →https://doi.org/10.1016/j.semcdb.2018.01.012openalex-snapshot
Phenotypic plasticity, canalization, and the origins of novelty: Evidence and mechanisms from amphibians
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Comparative genomics of nematodes
inferredcites →https://doi.org/10.1016/j.tplants.2010.09.008openalex-snapshot
Plant phenotypic plasticity in a changing climate
inferredcites →https://doi.org/10.1016/s0968-0004(02)02179-5openalex-snapshot
Evolution of protein kinase signaling from yeast to man
inferredcites →https://doi.org/10.1021/bm201032vopenalex-snapshot
Two Mechanisms for Supercontraction in Nephila Spider Dragline Silk
inferredcites →https://doi.org/10.1038/nature09164openalex-snapshot
Co-option of the hormone-signalling module dafachronic acid–DAF-12 in nematode evolution
inferredcites →https://doi.org/10.1038/nature14099openalex-snapshot
An Arabidopsis gene regulatory network for secondary cell wall synthesis
inferredcites →https://doi.org/10.1038/nature15256openalex-snapshot
Non-adaptive plasticity potentiates rapid adaptive evolution of gene expression in nature
inferredcites →https://doi.org/10.1038/nclimate2457openalex-snapshot
Physiological plasticity increases resilience of ectothermic animals to climate change
inferredcites →https://doi.org/10.1038/ncomms12337openalex-snapshot
Chromatin remodelling and antisense-mediated up-regulation of the developmental switch gene eud-1 control predatory feeding plasticity
inferredcites →https://doi.org/10.1038/ng.227openalex-snapshot
The Pristionchus pacificus genome provides a unique perspective on nematode lifestyle and parasitism
inferredcites →https://doi.org/10.1038/nmeth.1923openalex-snapshot
Fast gapped-read alignment with Bowtie 2
inferredcites →https://doi.org/10.1038/nmeth.2019openalex-snapshot
Fiji: an open-source platform for biological-image analysis
inferredcites →https://doi.org/10.1038/s41467-018-03384-9openalex-snapshot
Strong phenotypic plasticity limits potential for evolutionary responses to climate change
inferredcites →https://doi.org/10.1038/s41467-018-05612-8openalex-snapshot
A sulfotransferase dosage-dependently regulates mouthpart polyphenism in the nematode Pristionchus pacificus
inferredcites →https://doi.org/10.1038/s41467-018-07640-wopenalex-snapshot
Neurohormonal signaling via a sulfotransferase antagonizes insulin-like signaling to regulate a Caenorhabditis elegans stress response
inferredcites →https://doi.org/10.1038/s41598-017-07455-7openalex-snapshot
Environmental influence on Pristionchus pacificus mouth form through different culture methods
inferredcites →https://doi.org/10.1038/srep28838openalex-snapshot
Structural and functional characterization of the CAP domain of pathogen-related yeast 1 (Pry1) protein
inferredcites →https://doi.org/10.1046/j.1432-1033.2003.03891.xopenalex-snapshot
The astacin protein family in Caenorhabditis elegans
inferredcites →https://doi.org/10.1073/pnas.0501844102openalex-snapshot
Developmental plasticity and the origin of species differences
inferredcites →https://doi.org/10.1073/pnas.1209086109openalex-snapshot
Pathogen-Related Yeast (PRY) proteins and members of the CAP superfamily are secreted sterol-binding proteins
inferredcites →https://doi.org/10.1073/pnas.2133841100openalex-snapshot
Structure and function of the feed-forward loop network motif
inferredcites →https://doi.org/10.1073/pnas.92.15.7090openalex-snapshot
Conserved catalytic machinery and the prediction of a common fold for several families of glycosyl hydrolases.
inferredcites →https://doi.org/10.1086/590966openalex-snapshot
A Test of the “Flexible Stem” Model of Evolution: Ancestral Plasticity, Genetic Accommodation, and Morphological Divergence in the Threespine Stickleback Radiation
inferredcites →https://doi.org/10.1093/bioinformatics/btp324openalex-snapshot
Fast and accurate short read alignment with Burrows–Wheeler transform
inferredcites →https://doi.org/10.1093/bioinformatics/btp352openalex-snapshot
The Sequence Alignment/Map format and SAMtools
inferredcites →https://doi.org/10.1093/bioinformatics/bts635openalex-snapshot
STAR: ultrafast universal RNA-seq aligner
inferredcites →https://doi.org/10.1093/bioinformatics/btu033openalex-snapshot
RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies
inferredcites →https://doi.org/10.1093/molbev/mst010openalex-snapshot
MAFFT Multiple Sequence Alignment Software Version 7: Improvements in Performance and Usability
inferredcites →https://doi.org/10.1093/molbev/msx106openalex-snapshot
The Role of DAF-21/Hsp90 in Mouth-Form Plasticity in Pristionchus pacificus
inferredcites →https://doi.org/10.1093/molbev/msz171openalex-snapshot
Multiple Plasticity Regulators Reveal Targets Specifying an Induced Predatory Form in Nematodes
inferredcites →https://doi.org/10.1093/nar/gkv1344openalex-snapshot
The Pfam protein families database: towards a more sustainable future
inferredcites →https://doi.org/10.1093/oso/9780195122343.001.0001openalex-snapshot
Developmental Plasticity and Evolution
inferredcites →https://doi.org/10.1098/rsob.160332openalex-snapshot
The genetics of phenotypic plasticity in nematode feeding structures
inferredcites →https://doi.org/10.1098/rspb.2000.1132openalex-snapshot
Ultrastructure of the post–corpus of Zeldia punctata (Cephalobina) for analysis of the evolutionary framework of nematodes related to Caenorhabditis elegans (Rhabditina)
inferredcites →https://doi.org/10.1098/rspb.2011.0971openalex-snapshot
The role of developmental plasticity in evolutionary innovation
inferredcites →https://doi.org/10.1101/gad.10.3.301openalex-snapshot
Conservation of the hedgehog/patched signaling pathway from flies to mice: induction of a mouse patched gene by Hedgehog.
inferredcites →https://doi.org/10.1101/gad.14.12.1512openalex-snapshot
daf-12encodes a nuclear receptor that regulates the dauer diapause and developmental age inC. elegans
inferredcites →https://doi.org/10.1101/gr.097378.109openalex-snapshot
Gene regulatory networks and the role of robustness and stochasticity in the control of gene expression
inferredcites →https://doi.org/10.1101/gr.234872.118openalex-snapshot
Young genes have distinct gene structure, epigenetic profiles, and transcriptional regulation
inferredcites →https://doi.org/10.1101/gr.234971.118openalex-snapshot
Deep taxon sampling reveals the evolutionary dynamics of novel gene families in Pristionchus nematodes
inferredcites →https://doi.org/10.1101/gr.9.2.103openalex-snapshot
The Nuclear Receptor Superfamily Has Undergone Extensive Proliferation and Diversification in Nematodes
inferredcites →https://doi.org/10.1107/s2059798317011822openalex-snapshot
Structural insights into the interaction of the conserved mammalian proteins GAPR-1 and Beclin 1, a key autophagy protein
inferredcites →https://doi.org/10.1111/2041-210x.12035openalex-snapshot
geomorph: an r package for the collection and analysis of geometric morphometric shape data
inferredcites →https://doi.org/10.1111/ede.12030openalex-snapshot
Feeding plasticity in the nematode Pristionchus pacificus is influenced by sex and social context and is linked to developmental speed
inferredcites →https://doi.org/10.1126/science.1157174openalex-snapshot
Adaptive Phenotypic Plasticity in Response to Climate Change in a Wild Bird Population
inferredcites →https://doi.org/10.1126/science.aav9856openalex-snapshot
Small peptide–mediated self-recognition prevents cannibalism in predatory nematodes
inferredcites →https://doi.org/10.1139/cjz-79-1-16openalex-snapshot
Ultrastructure of the postcorpus of the esophagus of Teratocephalus lirellus (Teratocephalida) and its use for interpreting character evolution in Secernentea (Nematoda)
inferredcites →https://doi.org/10.1139/z00-174openalex-snapshot
Ultrastructure of the postcorpus of the esophagus of Teratocephalus lirellus (Teratocephalida) and its use for interpreting character evolution in Secernentea (Nematoda)
inferredcites →https://doi.org/10.1146/annurev-genet-120116-024456openalex-snapshot
Recent Advances in Behavioral (Epi)Genetics in Eusocial Insects
inferredcites →https://doi.org/10.1146/annurev.cellbio.20.010403.113126openalex-snapshot
THE WNT SIGNALING PATHWAY IN DEVELOPMENT AND DISEASE
inferredcites →https://doi.org/10.1163/156854109x456862openalex-snapshot
A phylogenetic tree of nematodes based on about 1200 full-length small subunit ribosomal DNA sequences
inferredcites →https://doi.org/10.1186/1471-213x-10-14openalex-snapshot
Characterization of the astacin family of metalloproteases in C. elegans
inferredcites →https://doi.org/10.1186/gb-2004-5-10-r80openalex-snapshot
Bioconductor: open software development for computational biology and bioinformatics
inferredcites →https://doi.org/10.1186/s13059-014-0550-8openalex-snapshot
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
inferredcites →https://doi.org/10.1210/er.2008-0032openalex-snapshot
The CAP Superfamily: Cysteine-Rich Secretory Proteins, Antigen 5, and Pathogenesis-Related 1 Proteins—Roles in Reproduction, Cancer, and Immune Defense
inferredcites →https://doi.org/10.1242/dev.00914openalex-snapshot
Genome-wide germline-enriched and sex-biased expression profiles in Caenorhabditis elegans
inferredcites →https://doi.org/10.1242/dev.122.8.2517openalex-snapshot
Stage-specific accumulation of the terminal differentiation factor LIN-29 during Caenorhabditis elegans development
inferredcites →https://doi.org/10.1242/dev.166272openalex-snapshot
Two independent sulfation processes regulate mouth-form plasticity in the nematodePristionchus pacificus
inferredcites →https://doi.org/10.1242/jeb.02165openalex-snapshot
Evolution of pharyngeal behaviors and neuronal functions in free-living soil nematodes
inferredcites →https://doi.org/10.1261/rna.041954.113openalex-snapshot
Genome-wide analysis of trans-splicing in the nematode Pristionchus pacificus unravels conserved gene functions for germline and dauer development in divergent operons
inferredcites →https://doi.org/10.1371/journal.pntd.0007396openalex-snapshot
Characterization of a non-sexual population of Strongyloides stercoralis with hybrid 18S rDNA haplotypes in Guangxi, Southern China
inferredcites →https://doi.org/10.1515/hsz-2012-0149openalex-snapshot
Functional and structural insights into astacin metallopeptidases
inferredcites →https://doi.org/10.1534/genetics.104.027953openalex-snapshot
Gene Interactions in Caenorhabditis elegans Define DPY-31 as a Candidate Procollagen C-Proteinase and SQT-3/ROL-4 as Its Predicted Major Target
inferredcites →https://doi.org/10.1621/nrs.10001openalex-snapshot
Post-Translational Modifications of Nuclear Receptors and Human Disease
inferredcites →https://doi.org/10.1895/wormbook.1.114.2openalex-snapshot
Pristionchus pacificus protocols
inferredcites →https://doi.org/10.7554/elife.05463openalex-snapshot
Rapid diversification associated with a macroevolutionary pulse of developmental plasticity
inferredcites →https://doi.org/10.7554/elife.46566openalex-snapshot
The transcription factor odd-paired regulates temporal identity in transit-amplifying neural progenitors via an incoherent feed-forward loop
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1098/rspb.2019.2595openalex-snapshot
Regulators of an ancient polyphenism evolved through episodic protein divergence and parallel gene radiations
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