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Socs36E Controls Niche Competition by Repressing MAPK Signaling in the Drosophila Testis

https://doi.org/10.1371/journal.pgen.1005815
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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/embr.201337799openalex-snapshot
Biased competition between Lgr5 intestinal stem cells driven by oncogenic mutation induces clonal expansion
inferredcites →https://doi.org/10.1002/jcp.22073openalex-snapshot
Competitiveness for the niche and mutual dependence of the germline and somatic stem cells in the Drosophila testis are regulated by the JAK/STAT signaling
inferredcites →https://doi.org/10.1007/s00018-014-1619-yopenalex-snapshot
SOCS proteins in regulation of receptor tyrosine kinase signaling
inferredcites →https://doi.org/10.1016/j.cell.2011.05.033openalex-snapshot
Strategies for Homeostatic Stem Cell Self-Renewal in Adult Tissues
inferredcites →https://doi.org/10.1016/j.cub.2003.10.063openalex-snapshot
Regulation of Stem Cell Maintenance and Transit Amplifying Cell Proliferation by TGF-β Signaling in Drosophila Spermatogenesis
inferredcites →https://doi.org/10.1016/j.cub.2007.06.048openalex-snapshot
Antagonistic Roles of Rac and Rho in Organizing the Germ Cell Microenvironment
inferredcites →https://doi.org/10.1016/j.devcel.2010.02.006openalex-snapshot
chinmo Is a Functional Effector of the JAK/STAT Pathway that Regulates Eye Development, Tumor Formation, and Stem Cell Self-Renewal in Drosophila
inferredcites →https://doi.org/10.1016/j.devcel.2011.06.018openalex-snapshot
Drosophila Stem Cell Niches: A Decade of Discovery Suggests a Unified View of Stem Cell Regulation
inferredcites →https://doi.org/10.1016/j.devcel.2014.10.004openalex-snapshot
The Jak-STAT Target Chinmo Prevents Sex Transformation of Adult Stem Cells in the Drosophila Testis Niche
inferredcites →https://doi.org/10.1016/j.devcel.2015.05.003openalex-snapshot
Somatic Cell Encystment Promotes Abscission in Germline Stem Cells following a Regulated Block in Cytokinesis
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.2013.05.003openalex-snapshot
The Nuclear Lamina Regulates Germline Stem Cell Niche Organization via Modulation of EGFR Signaling
inferredcites →https://doi.org/10.1016/j.ydbio.2008.11.014openalex-snapshot
SOCS36E specifically interferes with Sevenless signaling during Drosophila eye development
inferredcites →https://doi.org/10.1016/j.ymeth.2014.01.020openalex-snapshot
The regulation and functions of MAPK pathways in Drosophila
inferredcites →https://doi.org/10.1016/j.ymeth.2014.03.016openalex-snapshot
Strategies for exploring TGF-β signaling in Drosophila
inferredcites →https://doi.org/10.1016/s0092-8674(00)81462-2openalex-snapshot
Coordination of Growth and Cell Division in the Drosophila Wing
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/s0960-9822(01)00524-3openalex-snapshot
Identification of the first invertebrate interleukin JAK/STAT receptor, the Drosophila gene domeless
inferredcites →https://doi.org/10.1038/35037606openalex-snapshot
Somatic support cells restrict germline stem cell self-renewal and promote differentiation
inferredcites →https://doi.org/10.1038/35037613openalex-snapshot
Somatic control over the germline stem cell lineage during Drosophila spermatogenesis
inferredcites →https://doi.org/10.1038/ncb2086openalex-snapshot
Germline self-renewal requires cyst stem cells and stat regulates niche adhesion in Drosophila testes
inferredcites →https://doi.org/10.1038/sj.onc.1205618openalex-snapshot
SOCS36E, a novel Drosophila SOCS protein, suppresses JAK/STAT and EGF-R signalling in the imaginal wing disc
inferredcites →https://doi.org/10.1091/mbc.e13-05-0275openalex-snapshot
DrosophilaSOCS36E negatively regulates JAK/STAT pathway signaling via two separable mechanisms
inferredcites →https://doi.org/10.1101/gad.1320705openalex-snapshot
Genome-wide RNAi analysis of JAK/STAT signaling components in Drosophila
inferredcites →https://doi.org/10.1101/gad.192021.112openalex-snapshot
Oncogenic cooperation between SOCS family proteins and EGFR identified using a Drosophila epithelial transformation model
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.1097676openalex-snapshot
Regeneration of Male Germline Stem Cells by Spermatogonial Dedifferentiation in Vivo
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.1243148openalex-snapshot
Defining Stem Cell Dynamics in Models of Intestinal Tumor Initiation
inferredcites →https://doi.org/10.1126/science.277.5329.1103openalex-snapshot
In Situ Activation Pattern of Drosophila EGF Receptor Pathway During Development
inferredcites →https://doi.org/10.1146/annurev.immunol.22.091003.090312openalex-snapshot
T he R ole of S uppressors of C ytokine S ignaling (SOCS) P roteins in R egulation of the I mmune R esponse
inferredcites →https://doi.org/10.1186/1471-2121-5-38openalex-snapshot
Two Drosophila suppressors of cytokine signaling (SOCS) differentially regulate JAK and EGFR pathway activities
inferredcites →https://doi.org/10.1242/dev.01025openalex-snapshot
Gbb/Bmp signaling is essential for maintaining germline stem cells and for repressingbamtranscription in theDrosophilatestis
inferredcites →https://doi.org/10.1242/dev.056242openalex-snapshot
The stem cell niche: lessons from the Drosophila testis
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.117.4.1223openalex-snapshot
Analysis of genetic mosaics in developing and adult Drosophila tissues
inferredcites →https://doi.org/10.1242/dev.122.4.1125openalex-snapshot
hedgehog is required for the proliferation and specification of ovarian somatic cells prior to egg chamber formation in Drosophila
inferredcites →https://doi.org/10.1242/dev.124.19.3871openalex-snapshot
Ectopic activation of torpedo/Egfr, a Drosophila receptor tyrosine kinase, dorsalizes both the eggshell and the embryo
inferredcites →https://doi.org/10.1242/dev.129.19.4523openalex-snapshot
Signaling from germ cells mediated by therhomboidhomologstetorganizes encapsulation by somatic support cells
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.pone.0070678openalex-snapshot
A Temporal Signature of Epidermal Growth Factor Signaling Regulates the Differentiation of Germline Cells in Testes of Drosophila melanogaster
inferredcites →https://doi.org/10.15252/embj.201387500openalex-snapshot
Neutral competition of stem cells is skewed by proliferative changes downstream of Hh and Hpo

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.3155819openalex-extracted
Decoding the Regulatory Logic of the Drosophila Male Stem Cell System
inferred← citeshttps://doi.org/10.1002/arch.22065openalex-snapshot
Cloning of suppressor of cytokine signaling 7 from silkworm (Bombyx mori) and its response to the infection of Bombyx mori nucleopolyhedrovirus
inferred← citeshttps://doi.org/10.1002/arch.70017openalex-snapshot
ZnT35C Maintains Zinc Homeostasis to Regulate Spermatogenesis in Drosophila Testis
inferred← citeshttps://doi.org/10.1007/s10126-021-10083-yopenalex-snapshot
Genome-Wide Differential DNA Methylomes Provide Insights into the Infertility of Triploid Oysters
inferred← citeshttps://doi.org/10.1007/s40778-016-0048-2openalex-snapshot
Regulation of Stem Cells in Their Niche
inferred← citeshttps://doi.org/10.1016/b978-0-323-95424-2.00017-0openalex-snapshot
Spermatogenesis
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2026.03.001openalex-snapshot
Stem cell competition
inferred← citeshttps://doi.org/10.1016/j.cdev.2022.203822openalex-snapshot
Pvr regulates cyst stem cell division in the Drosophila testis niche, and has functions distinct from Egfr
inferred← citeshttps://doi.org/10.1016/j.celrep.2018.08.013openalex-snapshot
Decoding the Regulatory Logic of the Drosophila Male Stem Cell System
inferred← citeshttps://doi.org/10.1016/j.celrep.2019.12.086openalex-snapshot
EGFR Signaling Stimulates Autophagy to Regulate Stem Cell Maintenance and Lipid Homeostasis in the Drosophila Testis
inferred← citeshttps://doi.org/10.1016/j.celrep.2021.109553openalex-snapshot
Coordination of Tumor Growth and Host Wasting by Tumor-Derived Upd3
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.110679openalex-snapshot
Escargot controls somatic stem cell maintenance through the attenuation of the insulin receptor pathway in Drosophila
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.110774openalex-snapshot
Cell-cycle exit and stem cell differentiation are coupled through regulation of mitochondrial activity in the Drosophila testis
inferred← citeshttps://doi.org/10.1016/j.cub.2016.07.012openalex-snapshot
Occluding Junctions Maintain Stem Cell Niche Homeostasis in the Fly Testes
inferred← citeshttps://doi.org/10.1016/j.dci.2019.103561openalex-snapshot
Suppressors of cytokine signaling proteins as modulators of development and innate immunity of insects
inferred← citeshttps://doi.org/10.1016/j.devcel.2021.12.004openalex-snapshot
chinmo-mutant spermatogonial stem cells cause mitotic drive by evicting non-mutant neighbors from the niche
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2024.115948openalex-snapshot
Single-cell RNA sequencing analysis to evaluate antimony exposure effects on cell-lineage communications within the Drosophila testicular niche
inferred← citeshttps://doi.org/10.1016/j.ejcb.2023.151375openalex-snapshot
Rel governs loser elimination during stem cell competition in the Drosophila testis
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2018.06.028openalex-snapshot
Effect of dietary energy restriction and subsequent compensatory feeding on testicular transcriptome in developing rams
inferred← citeshttps://doi.org/10.1016/j.ydbio.2021.05.012openalex-snapshot
Merlin and expanded integrate cell signaling that regulates cyst stem cell proliferation in the Drosophila testis niche
inferred← citeshttps://doi.org/10.1016/j.yexcr.2019.02.024openalex-snapshot
Heterochromatin Protein 1 (HP1) inhibits stem cell proliferation induced by ectopic activation of the Jak/STAT pathway in the Drosophila testis
inferred← citeshttps://doi.org/10.1016/j.ygeno.2017.07.001openalex-snapshot
Genome-wide analysis of long non-coding RNAs and their role in postnatal porcine testis development
inferred← citeshttps://doi.org/10.1038/ncomms12149openalex-snapshot
Whole-animal genome-wide RNAi screen identifies networks regulating male germline stem cells in Drosophila
inferred← citeshttps://doi.org/10.1038/s41420-023-01391-4openalex-snapshot
Single-cell RNA sequencing reveals cell landscape following antimony exposure during spermatogenesis in Drosophila testes
inferred← citeshttps://doi.org/10.1038/s41598-019-42630-yopenalex-snapshot
Ectopic Dpp signaling promotes stem cell competition through EGFR signaling in the Drosophila testis
inferred← citeshttps://doi.org/10.1038/s41598-019-55728-0openalex-snapshot
Mitochondrial fission regulates germ cell differentiation by suppressing ROS-mediated activation of Epidermal Growth Factor Signaling in the Drosophila larval testis
inferred← citeshttps://doi.org/10.1093/genetics/iyag244openalex-snapshot
Niche cell positioning drives functional heterogeneity in the Drosophila testis stem cell niche
inferred← citeshttps://doi.org/10.1101/110619openalex-snapshot
Direct control of somatic stem cell proliferation by the Drosophila testis stem cell niche
inferred← citeshttps://doi.org/10.1101/2020.03.05.979161openalex-snapshot
Innate immune signalling drives loser cell elimination during stem cell competition in the Drosophila testis
inferred← citeshttps://doi.org/10.1101/2021.01.12.426342openalex-snapshot
Cell cycle exit and stem cell differentiation are coupled through regulation of mitochondrial activity in the Drosophila testis
inferred← citeshttps://doi.org/10.1101/2025.03.26.645575openalex-snapshot
The pioneer factor Zelda induces male-to-female somatic sex reversal in adult tissues
inferred← citeshttps://doi.org/10.1111/1744-7917.70072openalex-snapshot
Signaling pathways in Drosophila testis niche: Local signals that regulate stem cell fate
inferred← citeshttps://doi.org/10.1111/acel.14057openalex-snapshot
Single‐cell transcriptome characteristics of testicular terminal epithelium lineages during aging in the Drosophila
inferred← citeshttps://doi.org/10.1111/cpr.13648openalex-snapshot
A regulatory loop of JAK / STAT signalling and its downstream targets represses cell fate conversion and maintains male germline stem cell niche homeostasis
inferred← citeshttps://doi.org/10.1134/s1062360421010021openalex-snapshot
Somatic Cyst Cells as a Microenvironment for the Maintenance and Differentiation of Germline Cells in Drosophila Spermatogenesis
inferred← citeshttps://doi.org/10.1139/gen-2022-0069openalex-snapshot
Autophagy in cell fate decisions: knowledge gained fromDrosophila
inferred← citeshttps://doi.org/10.1155/2020/2846727openalex-snapshot
CG8005 Mediates Transit-Amplifying Spermatogonial Divisions via Oxidative Stress in Drosophila Testes
inferred← citeshttps://doi.org/10.1242/bio.059364openalex-snapshot
A kinase translocation reporter reveals real-time dynamics of ERK activity in Drosophila
inferred← citeshttps://doi.org/10.1242/dev.139782openalex-snapshot
Somatic stem cell differentiation is regulated by PI3K/Tor signaling in response to local cues
inferred← citeshttps://doi.org/10.1242/dev.156315openalex-snapshot
Direct control of somatic stem cell proliferation factors by the Drosophila testis stem cell niche
inferred← citeshttps://doi.org/10.1242/dev.167643openalex-snapshot
JAK/STAT signaling in stem cells and regeneration: fromDrosophilato vertebrates
inferred← citeshttps://doi.org/10.1242/dev.184259openalex-snapshot
Single-cyst transcriptome analysis of Drosophila male germline stem cell lineage
inferred← citeshttps://doi.org/10.1242/dev.202729openalex-snapshot
The Drosophila histone methyltransferase SET1 coordinates multiple signaling pathways in regulating male germline stem cell maintenance and differentiation
inferred← citeshttps://doi.org/10.1242/dev.204701openalex-snapshot
Antagonism between JAK/STAT downstream targets controls stem cell proliferation, cell fate conversion and tumorigenesis
inferred← citeshttps://doi.org/10.1371/journal.pgen.1006043openalex-snapshot
Maintenance of Stem Cell Niche Integrity by a Novel Activator of Integrin Signaling
inferred← citeshttps://doi.org/10.1371/journal.pgen.1006571openalex-snapshot
Enhancer of polycomb coordinates multiple signaling pathways to promote both cyst and germline stem cell differentiation in the Drosophila adult testis
inferred← citeshttps://doi.org/10.1371/journal.pgen.1007203openalex-snapshot
Chinmo prevents transformer alternative splicing to maintain male sex identity
inferred← citeshttps://doi.org/10.1371/journal.pgen.1009609openalex-snapshot
Germ cells commit somatic stem cells to differentiation following priming by PI3K/Tor activity in the Drosophila testis
inferred← citeshttps://doi.org/10.1530/rep-16-0347openalex-snapshot
A Drosophila toolkit for defining gene function in spermatogenesis
inferred← citeshttps://doi.org/10.21203/rs.3.rs-6588687/v1openalex-snapshot
Wnt6 is required for germline stem cell self-renewal and differentiation via regulating adhesion junction and ERK signaling in Drosophila testis
inferred← citeshttps://doi.org/10.3389/fcell.2026.1739650openalex-snapshot
Divergent functions of the RNA-binding protein, Mei-P26 in germline and somatic lineages of Drosophila testis
inferred← citeshttps://doi.org/10.3389/fendo.2017.00307openalex-snapshot
Cytokines in Male Fertility and Reproductive Pathologies: Immunoregulation and Beyond
inferred← citeshttps://doi.org/10.3389/fendo.2023.1165825openalex-snapshot
UBR4 deficiency causes male sterility and testis abnormal in Drosophila
inferred← citeshttps://doi.org/10.3390/ani11082263openalex-snapshot
Identification and Characterization of lncRNA and mRNA in Testes of Landrace and Hezuo Boars
inferred← citeshttps://doi.org/10.3390/ijms19124056openalex-snapshot
Drosophila Jak/STAT Signaling: Regulation and Relevance in Human Cancer and Metastasis
inferred← citeshttps://doi.org/10.3390/ijms27041884openalex-snapshot
Metabolic Regulation in the Maintenance of Drosophila Testis Stem Cells
inferred← citeshttps://doi.org/10.3390/life14101251openalex-snapshot
Mechanisms of Germline Stem Cell Competition across Species
inferred← citeshttps://doi.org/10.64898/2026.04.06.716791openalex-snapshot
Glia generate distinct visual processing centres by locally inhibiting ERK activity in an optic lobe neuroepithelium
inferred← citeshttps://doi.org/10.7554/elife.36095openalex-snapshot
JNK signaling triggers spermatogonial dedifferentiation during chronic stress to maintain the germline stem cell pool in the Drosophila testis
inferred← citeshttps://doi.org/10.7554/elife.78092openalex-snapshot
Differentiation signals from glia are fine-tuned to set neuronal numbers during development
inferred← citeshttps://doi.org/10.7554/elife.96446openalex-snapshot
Superoxide dismutases maintain niche homeostasis in stem cell populations
inferred← citeshttps://doi.org/10.7554/elife.96446.2openalex-snapshot
Superoxide Dismutases maintain niche homeostasis in stem cell populations
inferred← citeshttps://doi.org/10.7554/elife.96446.3openalex-snapshot
Superoxide Dismutases maintain niche homeostasis in stem cell populations
inferred← citeshttps://doi.org/10.7554/elife.96446.4openalex-snapshot
Superoxide dismutases maintain niche homeostasis in stem cell populations
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