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Innate immune signalling drives loser cell elimination during stem cell competition in the Drosophila testis

https://doi.org/10.1101/2020.03.05.979161
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1016/0012-1606(81)90261-xopenalex-snapshot
Differential mitotic rates and patterns of growth in compartments in the Drosophila wing
inferredcites →https://doi.org/10.1016/0092-8674(85)90274-0openalex-snapshot
Establishment of dorsal-ventral polarity in the Drosophila embryo: Genetic studies on the role of the Toll gene product
inferredcites →https://doi.org/10.1016/j.ceb.2018.08.002openalex-snapshot
Cell competition in development: information from flies and vertebrates
inferredcites →https://doi.org/10.1016/j.cell.2010.09.016openalex-snapshot
Intestinal Crypt Homeostasis Results from Neutral Competition between Symmetrically Dividing Lgr5 Stem Cells
inferredcites →https://doi.org/10.1016/j.cell.2013.09.007openalex-snapshot
MEF2 Is an In Vivo Immune-Metabolic Switch
inferredcites →https://doi.org/10.1016/j.celrep.2019.06.037openalex-snapshot
Three-Dimensional Genomic Structure and Cohesin Occupancy Correlate with Transcriptional Activity during Spermatogenesis
inferredcites →https://doi.org/10.1016/j.cmet.2014.01.012openalex-snapshot
Supercompetitor Status of Drosophila Myc Cells Requires p53 as a Fitness Sensor to Reprogram Metabolism and Promote Viability
inferredcites →https://doi.org/10.1016/j.dci.2008.12.002openalex-snapshot
The N-terminal half of the Drosophila Rel/NF-κB factor Relish, REL-68, constitutively activates transcription of specific Relish target genes
inferredcites →https://doi.org/10.1016/j.dci.2012.10.007openalex-snapshot
Transcription factor zfh1 downregulates Drosophila Imd pathway
inferredcites →https://doi.org/10.1016/j.devcel.2018.08.001openalex-snapshot
Spatially Restricted Regulation of Spätzle/Toll Signaling during Cell Competition
inferredcites →https://doi.org/10.1016/j.stem.2008.05.001openalex-snapshot
Zfh-1 Controls Somatic Stem Cell Self-Renewal in the Drosophila Testis and Nonautonomously Influences Germline Stem Cell Self-Renewal
inferredcites →https://doi.org/10.1016/j.stem.2019.07.002openalex-snapshot
Defining Adult Stem Cell Function at Its Simplest: The Ability to Replace Lost Cells through Mitosis
inferredcites →https://doi.org/10.1016/j.ydbio.2006.02.030openalex-snapshot
Development of the male germline stem cell niche in Drosophila
inferredcites →https://doi.org/10.1016/j.ydbio.2012.09.009openalex-snapshot
Jak-STAT regulation of cyst stem cell development in the Drosophila testis
inferredcites →https://doi.org/10.1016/s0092-8674(04)00214-4openalex-snapshot
Drosophila Myc Regulates Organ Size by Inducing Cell Competition
inferredcites →https://doi.org/10.1016/s0092-8674(04)00262-4openalex-snapshot
dMyc Transforms Cells into Super-Competitors
inferredcites →https://doi.org/10.1016/s0896-6273(00)80701-1openalex-snapshot
Mosaic Analysis with a Repressible Cell Marker for Studies of Gene Function in Neuronal Morphogenesis
inferredcites →https://doi.org/10.1016/s1097-2765(00)80392-5openalex-snapshot
Relish, a Central Factor in the Control of Humoral but Not Cellular Immunity in Drosophila
inferredcites →https://doi.org/10.1038/416755aopenalex-snapshot
Cells compete for Decapentaplegic survival factor to prevent apoptosis in Drosophila wing development
inferredcites →https://doi.org/10.1038/emboj.2012.106openalex-snapshot
Drosophila midgut homeostasis involves neutral competition between symmetrically dividing intestinal stem cells
inferredcites →https://doi.org/10.1038/nature07173openalex-snapshot
Multipotent somatic stem cells contribute to the stem cell niche in the Drosophila testis
inferredcites →https://doi.org/10.1038/ncomms10473openalex-snapshot
The novel tumour suppressor Madm regulates stem cell competition in the Drosophila testis
inferredcites →https://doi.org/10.1038/nmeth.2019openalex-snapshot
Fiji: an open-source platform for biological-image analysis
inferredcites →https://doi.org/10.1038/nri2194openalex-snapshot
The Drosophila systemic immune response: sensing and signalling during bacterial and fungal infections
inferredcites →https://doi.org/10.1038/s41467-017-00485-9openalex-snapshot
miR-9a modulates maintenance and ageing of Drosophila germline stem cells by limiting N-cadherin expression
inferredcites →https://doi.org/10.1093/bioinformatics/btz931openalex-snapshot
ShinyGO: a graphical gene-set enrichment tool for animals and plants
inferredcites →https://doi.org/10.1093/emboj/17.5.1217openalex-snapshot
A drosomycin–GFP reporter transgene reveals a local immune response in Drosophila that is not dependent on the Toll pathway
inferredcites →https://doi.org/10.1126/science.1066700openalex-snapshot
Control of Stem Cell Self-Renewal in Drosophila Spermatogenesis by JAK-STAT Signaling
inferredcites →https://doi.org/10.1126/science.1066707openalex-snapshot
Stem Cell Self-Renewal Specified by JAK-STAT Activation in Response to a Support Cell Cue
inferredcites →https://doi.org/10.1126/science.1176817openalex-snapshot
JAK-STAT Signal Inhibition Regulates Competition in the Drosophila Testis Stem Cell Niche
inferredcites →https://doi.org/10.1126/science.1258236openalex-snapshot
An ancient defense system eliminates unfit cells from developing tissues during cell competition
inferredcites →https://doi.org/10.1146/annurev-biochem-062917-012341openalex-snapshot
Defining Adult Stem Cells by Function, not by Phenotype
inferredcites →https://doi.org/10.1242/dev.075242openalex-snapshot
Hh signalling is essential for somatic stem cell maintenance in theDrosophilatestis niche
inferredcites →https://doi.org/10.1242/dev.086413openalex-snapshot
Hedgehog is required for CySC self-renewal but does not contribute to the GSC niche in the Drosophila testis
inferredcites →https://doi.org/10.1242/dev.156315openalex-snapshot
Direct control of somatic stem cell proliferation factors by the Drosophila testis stem cell niche
inferredcites →https://doi.org/10.1242/dev.167486openalex-snapshot
Cell competition: the winners and losers of fitness selection
inferredcites →https://doi.org/10.1242/jcs.128926openalex-snapshot
Phosphorylation of the Smo tail is controlled by membrane localization and is dispensable for clustering
inferredcites →https://doi.org/10.1371/journal.pbio.1000422openalex-snapshot
Involvement of Lgl and Mahjong/VprBP in Cell Competition
inferredcites →https://doi.org/10.1371/journal.pbio.1000441openalex-snapshot
A Short Receptor Downregulates JAK/STAT Signalling to Control the Drosophila Cellular Immune Response
inferredcites →https://doi.org/10.1371/journal.pgen.1004713openalex-snapshot
Coordinate Regulation of Stem Cell Competition by Slit-Robo and JAK-STAT Signaling in the Drosophila Testis
inferredcites →https://doi.org/10.1371/journal.pgen.1005815openalex-snapshot
Socs36E Controls Niche Competition by Repressing MAPK Signaling in the Drosophila Testis
inferredcites →https://doi.org/10.1371/journal.ppat.0030026openalex-snapshot
A Specific Primed Immune Response in Drosophila Is Dependent on Phagocytes
inferredcites →https://doi.org/10.15252/embj.201387500openalex-snapshot
Neutral competition of stem cells is skewed by proliferative changes downstream of Hh and Hpo
inferredcites →https://doi.org/10.32614/cran.package.pmcmrplusopenalex-snapshot
PMCMRplus: Calculate Pairwise Multiple Comparisons of Mean Rank Sums Extended
inferredcites →https://doi.org/10.7554/elife.19942openalex-snapshot
Genome-wide identification of neuronal activity-regulated genes in Drosophila
inferredcites →https://doi.org/10.7554/elife.19942.040openalex-snapshot
Author response: Genome-wide identification of neuronal activity-regulated genes in Drosophila
inferredcites →https://doi.org/10.7554/elife.35954openalex-snapshot
A population of adult satellite-like cells in Drosophila is maintained through a switch in RNA-isoforms
inferredcites →https://doi.org/10.7554/elife.35954.020openalex-snapshot
Author response: A population of adult satellite-like cells in Drosophila is maintained through a switch in RNA-isoforms

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1101/2020.02.24.962639openalex-snapshot
Transcriptome analysis of somatic cell populations in the Drosophila testis links metabolism and stemness
inferred← citeshttps://doi.org/10.1101/2021.04.06.438672openalex-snapshot
The Drosophila TNF Eiger contributes to Myc super-competition independent of JNK activity
inferred← citeshttps://doi.org/10.1101/2022.12.16.520841openalex-snapshot
An important role for triglyceride in regulating spermatogenesis
inferred← citeshttps://doi.org/10.1242/dev.205006openalex-snapshot
Toll receptors mediate tissue intrinsic surveillance against aberrant cells by detecting cell fate aberrations
inferred← citeshttps://doi.org/10.7554/elife.87523openalex-snapshot
An important role for triglyceride in regulating spermatogenesis
inferred← citeshttps://doi.org/10.7554/elife.87523.1openalex-snapshot
An important role for triglyceride in regulating spermatogenesis
inferred← citeshttps://doi.org/10.7554/elife.87523.1.sa0openalex-snapshot
Reviewer #3 (Public Review): An important role for triglyceride in regulating spermatogenesis
inferred← citeshttps://doi.org/10.7554/elife.87523.1.sa1openalex-snapshot
Reviewer #2 (Public Review): An important role for triglyceride in regulating spermatogenesis
inferred← citeshttps://doi.org/10.7554/elife.87523.1.sa2openalex-snapshot
Reviewer #1 (Public Review): An important role for triglyceride in regulating spermatogenesis
inferred← citeshttps://doi.org/10.7554/elife.87523.1.sa3openalex-snapshot
eLife Assessment: An important role for triglyceride in regulating spermatogenesis
inferred← citeshttps://doi.org/10.7554/elife.87523.1.sa4openalex-snapshot
Author Response: An important role for triglyceride in regulating spermatogenesis
inferred← citeshttps://doi.org/10.7554/elife.87523.2openalex-snapshot
An important role for triglyceride in regulating spermatogenesis
inferred← citeshttps://doi.org/10.7554/elife.87523.3openalex-snapshot
An important role for triglyceride in regulating spermatogenesis
inferred← citeshttps://doi.org/10.7554/elife.87523.4openalex-snapshot
An important role for triglyceride in regulating spermatogenesis
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