HCSGD entry for GSC


1. General information

Official gene symbolGSC
Entrez ID145258
Gene full namegoosecoid homeobox
Other gene symbols
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

color bar
This gene isn't in PPI subnetwork.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0000122Negative regulation of transcription from RNA polymerase II promoterIEAbiological_process
GO:0001085RNA polymerase II transcription factor bindingISSmolecular_function
GO:0001103RNA polymerase II repressing transcription factor bindingISSmolecular_function
GO:0003700Sequence-specific DNA binding transcription factor activityIEAmolecular_function
GO:0005634NucleusIEAcellular_component
GO:0005667Transcription factor complexIEAcellular_component
GO:0007369GastrulationNASbiological_process
GO:0021904Dorsal/ventral neural tube patterningIEAbiological_process
GO:0023019Signal transduction involved in regulation of gene expressionIEAbiological_process
GO:0030178Negative regulation of Wnt signaling pathwayIEAbiological_process
GO:0030900Forebrain developmentIEAbiological_process
GO:0042474Middle ear morphogenesisISSbiological_process
GO:0043565Sequence-specific DNA bindingIEAmolecular_function
GO:0048644Muscle organ morphogenesisIEAbiological_process
GO:0048704Embryonic skeletal system morphogenesisIEAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.34402842980.75482801570.99999024731.0000000000

  • Individual experiment result
    ( "-" represent NA in the specific microarray platform )

Data sourceUp or downLog fold change
GSE11954Up0.0994219017
GSE13712_SHEARDown-0.1118752203
GSE13712_STATICUp0.2135233159
GSE19018Down-0.1272927956
GSE19899_A1Down-0.1050661477
GSE19899_A2Up0.0166255309
PubMed_21979375_A1Up0.0538919368
PubMed_21979375_A2Up0.1416041219
GSE35957Down-0.2749401047
GSE36640Down-0.0650180891
GSE54402Down-0.0628127507
GSE9593Up0.0279941063
GSE43922Up0.3210765667
GSE24585Down-0.0273712702
GSE37065Down-0.0482059071
GSE28863_A1Down-0.1257912240
GSE28863_A2Up0.0419702793
GSE28863_A3Up0.5059554176
GSE28863_A4Up0.0203947553
GSE48662Up0.5670116419

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Not regulated by compounds

  • Drugs

Not regulated by drugs

  • MicroRNAs

    • mirTarBase

MiRNA_name

mirBase ID

miRTarBase ID

Experiment

Support type

References (Pubmed ID)

hsa-miR-375MIMAT0000728MIRT019699MicroarrayFunctional MTI (Weak)20215506
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    • mirRecord
No target information from mirRecord

6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 4 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

25470527Insulin signaling, which controls cellular nutrient sensing and organismal aging, regulates the G2 phase of Drosophila female germ line stem cell (GSC) division cycle in response to diet; furthermore, this signaling pathway is attenuated with age
25470527Here, we report that aging results in the accumulation of tumorous GSCs, accompanied by a decline in GSC number and proliferation rate
25470527In addition, GSC tumors (which escape the normal stem cell regulatory microenvironment, known as the niche) still respond to aging in a similar manner to normal GSCs, suggesting that niche signals are not required for GSCs to sense or respond to aging
25157949If GSCs were present in adult female ovaries, it could be postulated that the occurrence of menopause is not due to the exhaustion of a fixed supply of oocytes but instead is a result of GSC and somatic cell aging
18371381BMP signaling activity from the niche significantly decreases with age, and increasing BMP signaling can prolong GSC life span and promote their proliferation
18371381Finally, overexpression of SOD, an enzyme that helps eliminate free oxygen species, in either GSCs or their niche alone can prolong GSC life span and increase GSC proliferation
18267001Here we show in female Drosophila that germline stem cell (GSC) division rate progressively declines with age, which is accompanied by reduced decapentaplegic (dpp) niche signaling pathway activation within GSCs
18267001Genetically increasing dpp expression delays GSC activity decline and transiently increases egg production
18267001We conclude that age-related decline of reproduction is caused by both decreased GSC activity and increased incidence of cell death during oogenesis, while decreased GSC activity is attributed to declined signaling from the regulatory niche
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