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Direct control of somatic stem cell proliferation by the Drosophila testis stem cell niche

https://doi.org/10.1101/110619
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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.21411openalex-snapshot
Genes of Hippo signaling network act unconventionally in the control of germline proliferation in Drosophila
inferredcites →https://doi.org/10.1007/s00018-012-0935-3openalex-snapshot
Evolutionary functional analysis and molecular regulation of the ZEB transcription factors
inferredcites →https://doi.org/10.1016/0925-4773(91)90048-bopenalex-snapshot
The Drosophila zfh-1 and zfh-2 genes encode novel proteins containing both zinc-finger and homeodomain motifs
inferredcites →https://doi.org/10.1016/0925-4773(91)90049-copenalex-snapshot
The embryonic expression patterns of zfh-1 and zfh-2, two Drosophila genes encoding novel zinc-finger homeodomain proteins
inferredcites →https://doi.org/10.1016/j.cell.2014.02.013openalex-snapshot
Nice Neighborhood: Emerging Concepts of the Stem Cell Niche
inferredcites →https://doi.org/10.1016/j.cub.2003.09.033openalex-snapshot
Dpp Signaling Silences bam Transcription Directly to Establish Asymmetric Divisions of Germline Stem Cells
inferredcites →https://doi.org/10.1016/j.devcel.2008.01.006openalex-snapshot
The TEAD/TEF Family of Transcription Factor Scalloped Mediates Hippo Signaling in Organ Size Control
inferredcites →https://doi.org/10.1016/j.devcel.2009.12.011openalex-snapshot
Kibra Is a Regulator of the Salvador/Warts/Hippo Signaling Network
inferredcites →https://doi.org/10.1016/j.devcel.2009.12.012openalex-snapshot
Kibra Functions as a Tumor Suppressor Protein that Regulates Hippo Signaling in Conjunction with Merlin and Expanded
inferredcites →https://doi.org/10.1016/j.devcel.2009.12.013openalex-snapshot
The WW Domain Protein Kibra Acts Upstream of Hippo in Drosophila
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.2013.05.020openalex-snapshot
Cell-Type-Specific Profiling of Gene Expression and Chromatin Binding without Cell Isolation: Assaying RNA Pol II Occupancy in Neural Stem Cells
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.gde.2016.05.011openalex-snapshot
Zebrafish fin and heart: what's special about regeneration?
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/s0012-1606(03)00127-1openalex-snapshot
A somatic role for eyes absent (eya) and sine oculis (so) in drosophila spermatocyte development
inferredcites →https://doi.org/10.1016/s0092-8674(02)00824-3openalex-snapshot
salvador Promotes Both Cell Cycle Exit and Apoptosis in Drosophila and Is Mutated in Human Cancer Cell Lines
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/10.1038/459927aopenalex-snapshot
Unlocking the secrets of the genome
inferredcites →https://doi.org/10.1038/nature09990openalex-snapshot
A cis-regulatory map of the Drosophila genome
inferredcites →https://doi.org/10.1038/nature14602openalex-snapshot
Nanotubes mediate niche–stem-cell signalling in the Drosophila testis
inferredcites →https://doi.org/10.1038/nbt957openalex-snapshot
Correction of multi-gene deficiency in vivo using a single 'self-cleaving' 2A peptide–based retroviral vector
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/ncb3385openalex-snapshot
Metabolic regulation of stem cell function in tissue homeostasis and organismal ageing
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/ncomms1426openalex-snapshot
Local BMP receptor activation at adherens junctions in the Drosophila germline stem cell niche
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/nmeth.2019openalex-snapshot
Fiji: an open-source platform for biological-image analysis
inferredcites →https://doi.org/10.1038/s41598-017-02768-zopenalex-snapshot
Merlin is required for coordinating proliferation of two stem cell lineages in the Drosophila testis
inferredcites →https://doi.org/10.1073/pnas.1405500111openalex-snapshot
Optimized CRISPR/Cas tools for efficient germline and somatic genome engineering in Drosophila
inferredcites →https://doi.org/10.1073/pnas.96.12.6683openalex-snapshot
ZEB represses transcription through interaction with the corepressor CtBP
inferredcites →https://doi.org/10.1083/jcb.201309141openalex-snapshot
Coupling of Hedgehog and Hippo pathways promotes stem cell maintenance by stimulating proliferation
inferredcites →https://doi.org/10.1093/bioinformatics/btv386openalex-snapshot
damidseq_pipeline: an automated pipeline for processing DamID sequencing datasets
inferredcites →https://doi.org/10.1093/nar/gkv1194openalex-snapshot
PANTHER version 10: expanded protein families and functions, and analysis tools
inferredcites →https://doi.org/10.1101/cshperspect.a019224openalex-snapshot
Control of Organ Growth by Patterning and Hippo Signaling inDrosophila
inferredcites →https://doi.org/10.1101/gad.274027.115openalex-snapshot
Mechanisms of Hippo pathway regulation
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.1140861openalex-snapshot
Male and Female Drosophila Germline Stem Cells: Two Versions of Immortality
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.1232542openalex-snapshot
Genome-Wide Quantitative Enhancer Activity Maps Identified by STARR-seq
inferredcites →https://doi.org/10.1126/science.290.5490.328openalex-snapshot
A Niche Maintaining Germ Line Stem Cells in the Drosophila Ovary
inferredcites →https://doi.org/10.1126/scisignal.2004208openalex-snapshot
Hippo Gains Weight: Added Insights and Complexity to Pathway Control
inferredcites →https://doi.org/10.1134/s0026893314010087openalex-snapshot
Transcription factor Comr acts as a direct activator in the genetic program controlling spermatogenesis in D. melanogaster
inferredcites →https://doi.org/10.1186/1471-2105-11-237openalex-snapshot
ChIPpeakAnno: a Bioconductor package to annotate ChIP-seq and ChIP-chip data
inferredcites →https://doi.org/10.1186/1471-2164-10-22openalex-snapshot
BioMart – biological queries made easy
inferredcites →https://doi.org/10.1186/gb-2010-11-10-r106openalex-snapshot
Differential expression analysis for sequence count data
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.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.125.4.655openalex-snapshot
zfh-1 is required for germ cell migration and gonadal mesoderm development in Drosophila
inferredcites →https://doi.org/10.1242/dev.126.14.3241openalex-snapshot
The Drosophila homeobox genes zfh-1 and even-skipped are required for cardiac-specific differentiation of a numb-dependent lineage decision
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/10.15252/embj.201387500openalex-snapshot
Neutral competition of stem cells is skewed by proliferative changes downstream of Hh and Hpo
inferredcites →https://doi.org/10.1534/genetics.108.090563openalex-snapshot
Efficient Ends-Out Gene Targeting In Drosophila
inferredcites →https://doi.org/10.1534/genetics.113.160713openalex-snapshot
Highly Specific and Efficient CRISPR/Cas9-Catalyzed Homology-Directed Repair in Drosophila

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

inferred← citeshttps://doi.org/10.7554/elife.30107openalex-snapshot
Identification and functional characterization of muscle satellite cells in Drosophila
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