HCSGD entry for PTRF


1. General information

Official gene symbolPTRF
Entrez ID284119
Gene full namepolymerase I and transcript release factor
Other gene symbolsCAVIN CAVIN1 CGL4 cavin-1
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

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3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0005515Protein bindingIPImolecular_function
GO:0005634NucleusIDAcellular_component
GO:0005654NucleoplasmTAScellular_component
GO:0005737CytoplasmIDAcellular_component
GO:0005739MitochondrionIDAcellular_component
GO:0005783Endoplasmic reticulumIEAcellular_component
GO:0005829CytosolIEAcellular_component
GO:0005901CaveolaIDAcellular_component
GO:0006355Regulation of transcription, DNA-templatedIEAbiological_process
GO:0006360Transcription from RNA polymerase I promoterTASbiological_process
GO:0006361Transcription initiation from RNA polymerase I promoterIDAbiological_process
GO:0006363Termination of RNA polymerase I transcriptionIDA TASbiological_process
GO:0010467Gene expressionTASbiological_process
GO:0042134RRNA primary transcript bindingIDAmolecular_function
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.44751303520.00848699520.99999024730.1841600989

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

Data sourceUp or downLog fold change
GSE11954Down-0.7419809144
GSE13712_SHEARDown-0.2158250180
GSE13712_STATICDown-0.2594405395
GSE19018Down-0.1010584096
GSE19899_A1Down-1.3924217161
GSE19899_A2Down-0.8404625505
PubMed_21979375_A1Down-1.7480518693
PubMed_21979375_A2Down-1.5167519677
GSE35957Up0.0397986468
GSE36640Up0.1782825365
GSE54402Down-0.7248885125
GSE9593Up0.3923241923
GSE43922Down-0.5994284757
GSE24585Up0.2278367596
GSE37065Down-0.8122713386
GSE28863_A1Up0.7699682425
GSE28863_A2Up0.3693051699
GSE28863_A3Up0.4813751299
GSE28863_A4Up0.2182330074
GSE48662Down-0.1651004156

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-124-3pMIMAT0000422MIRT023054Proteomics;MicroarrayFunctional MTI (Weak)18668037
hsa-miR-342-3pMIMAT0000753MIRT043709CLASHFunctional MTI (Weak)23622248
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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: 5 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

25407919Senescent EC induced by either the overexpression of ARHGAP18/SENEX or by H(2)O(2) showed significantly increased numbers of caveolae and associated proteins Caveolin-1, cavin-1 and cavin-2
24812087Polymerase I and transcript release factor (PTRF) regulates adipocyte differentiation and determines adipose tissue expandability
24812087Using proteomics, we compared subcutaneous adipose tissues from mice in these groups and found that the expression of PTRF (polymerase I and transcript release factor) associated selectively with their glucose tolerance status
24812087Lentiviral and pharmacologically overexpressed PTRF, whose function is critical for caveola formation, compromised adipocyte differentiation of cultured 3T3-L1cells
24812087In human adipose tissue, PTRF mRNA levels positively correlated with markers of lipolysis and cellular senescence
24812087Furthermore, a negative relationship between telomere length and PTRF mRNA levels was observed in human subcutaneous fat
24812087PTRF is associated with limited adipose tissue expansion underpinning the key role of caveolae in adipocyte regulation
24812087Furthermore, PTRF may be a suitable adipocyte marker for predicting pathological obesity and inform clinical management
24471649Increased polymerase I and transcript release factor (Cavin-1) expression attenuates platelet-derived growth factor receptor signalling in senescent human fibroblasts
24471649Previously, we showed that the essential caveolar component polymerase I and transcript release factor (PTRF) was upregulated and promoted caveolae formation in senescent cells
24471649In addition, we found that overexpression of PTRF increased the number of caveolae and induced cellular senescence
24471649Herein, we investigated the role of PTRF in the regulation of platelet-derived growth factor (PDGF) signalling in young and senescent cells
24471649We first confirmed that PTRF was upregulated in senescent human fibroblasts and aged mouse tissues
24471649Furthermore, our results show that PTRF interacts with PDGFRs and this interaction is increased in senescent cells
24471649These results suggest that the unresponsiveness of senescent fibroblasts to PDGF stimulation may be due to increased levels of PTRF and the formation of caveolae, which, in turn sequester growth receptors, such as PDGFR and its signalling molecules
23941874Caveolin-1/PTRF upregulation constitutes a mechanism for mediating p53-induced cellular senescence: implications for evidence-based therapy of delayed wound healing in diabetes
23941874Mechanistically, we found that diabetes-induced oxidative stress upregulated caveolin-1 (Cav-1) and PTRF expression, which in turn sequestered Mdm2 away from p53
23941874Intriguingly, we confirmed that the targeted depletion of Cav-1 or PTRF using siRNA- or Vivo-Morpholino antisense-based gene therapy markedly inhibited diabetes/oxidative stress-induced premature senescence and also accelerated tissue repair in this disease state
21445100Regulation of cellular senescence by the essential caveolar component PTRF/Cavin-1
21445100Polymerase I and transcript release factor (PTRF, also known as Cavin-1) is an essential component in the biogenesis and function of caveolae
21445100Here, we show that PTRF expression is increased in senescent human fibroblasts
21445100Importantly, overexpression of PTRF induced features characteristic of cellular senescence, whereas reduced PTRF expression extended the cellular replicative lifespan
21445100Interestingly, we found that PTRF localized primarily to the nuclei of young and quiescent WI-38 human fibroblasts, but translocated to the cytosol and plasma membrane during cellular senescence
21445100Our data suggest that the role of PTRF in cellular senescence is dependent on its targeting to caveolae and its interaction with caveolin-1, which appeared to be regulated by the phosphorylation of PTRF
21445100Taken together, our findings identify PTRF as a novel regulator of cellular senescence that acts through the p53/p21 and caveolar pathways
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