HCSGD entry for RPE


1. General information

Official gene symbolRPE
Entrez ID6120
Gene full nameribulose-5-phosphate-3-epimerase
Other gene symbolsRPE2-1
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

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This gene isn't in Literature mining network.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0004750Ribulose-phosphate 3-epimerase activityEXP IDA IEAmolecular_function
GO:0005829CytosolTAScellular_component
GO:0005975Carbohydrate metabolic processIDA IEA TASbiological_process
GO:0006098Pentose-phosphate shuntIDA IEA TASbiological_process
GO:0016857Racemase and epimerase activity, acting on carbohydrates and derivativesIEAmolecular_function
GO:0042802Identical protein bindingIPImolecular_function
GO:0042803Protein homodimerization activityIPImolecular_function
GO:0044281Small molecule metabolic processTASbiological_process
GO:0046872Metal ion bindingIDA IEAmolecular_function
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.97383024580.14540071430.99999024730.7355549106

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

Data sourceUp or downLog fold change
GSE11954Down-0.1368049143
GSE13712_SHEARUp0.0862250682
GSE13712_STATICUp0.2170652871
GSE19018Down-0.0703555541
GSE19899_A1Down-0.1257314591
GSE19899_A2Down-0.2169863703
PubMed_21979375_A1Down-0.2078564380
PubMed_21979375_A2Down-0.3965044686
GSE35957Up0.0876428627
GSE36640Down-0.2836181382
GSE54402Up0.0045959282
GSE9593Up0.0000232346
GSE43922Down-0.0437894267
GSE24585Down-0.0205771934
GSE37065Down-0.1717285494
GSE28863_A1--
GSE28863_A2--
GSE28863_A3--
GSE28863_A4--
GSE48662Down-0.4526340760

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-142-3pMIMAT0000434MIRT021632MicroarrayFunctional MTI (Weak)17612493
hsa-miR-1260bMIMAT0015041MIRT052778CLASHFunctional 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: 19 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

27917303METHODS: The expression of miR-146a and miR-146b was examined in the neuroretina and RPE/choroid in mice aged from 2 months to 24 months
27917303RESULTS: miR-146a and miR-146b was upregulated during aging of RPE/choroid but not neuroretina, supporting tissue-specific regulation of aging-related miRNAs in retinal tissues
27917303CONCLUSIONS: Elevation of miR-146a and miR-146b in the aging RPE/choroid but not neuroretina suggests a role for miRNAs in inflammaging in the RPE/choroid
27115165Expressions of IL-6 and IL-8 in RPE/choroid were analyzed using RT-PCR
27115165Expressions of proinflammatory IL-6 and IL-8 were significantly upregulated in RPE/choroid of aged SAMP8 mice
26934949However, the molecular mechanisms underlying RPE dysfunction are not well understood
25385658The accumulation of vacuoles and the loss of basal infoldings in the RPE were identified using an electron microscope
25385658In conclusion, our results confirm the effects of Abeta(1-42) peptide on RPE senescence in vivo
23964074The P2X7R was expressed on apical and basolateral membranes of mouse RPE; mRNA expression of P2X7R and extracellular ATP marker NTPDase1 was raised in RPE tissue from the ABCA4(-/-) mouse model of Stargardt's retinal degeneration
23169885HFE is expressed in retinal pigment epithelium (RPE), and Hfe(-/-) mice develop age-related iron accumulation and retinal degeneration associated with RPE hyperproliferation
23169885Here, the mechanism underlying the hyperproliferative phenotype in RPE was investigated
21526120It is thought that some peripheral cells migrate centrally to correct age-related central RPE loss
21526120Low density RPE cultures obtained from adult mice revealed significantly greater levels of proliferation when derived from peripheral compared to central tissue, but this significance declined with increasing culture density
21526120A range of other genes were investigated both in vivo and in vitro associated with RPE proliferation in order to identify gene expression differences between the centre and the periphery
19932443Autofluorescence of the A2E fluorophore within retinal pigment epithelial (RPE) lipofuscin affords the opportunity for noninvasive evaluation of age- and disease-related pathophysiological changes in the human retina
19932443RESULTS: The data reveal improvements in all measures of visual function, subjective improvement in vision and mental functioning on the VFQ 25, and visible clearing of RPE lipofuscin
19458325This study was designed to improve the understanding of proteomic changes that underlie RPE senescence
19274853The loss of vision involves primarily a progressive degeneration and cell death of postmitotic retinal pigment epithelial cells (RPE), which secondarily evokes adverse effects on photoreceptor cells
19171648Therefore, reduction of oxidative stress and minimizing TGF-beta may help to prevent senescence-associated changes in the RPE as seen in early age-related macular degeneration
18817863Immunofluorescence assay revealed that the 20S proteasome was concentrated in RPE nucleus, and redistributed partly to the peri-nuclear regions in old RPE passages
18817863Further analysis of the proteasome-to-oxidized protein ratio indicated a preferred protection of the RPE nuclear proteins by the 20S proteasome, which also subsided remarkably as a function of the cell ageing
18385095The protective effect of quercetin against oxidative stress in the human RPE in vitro
18226607The prime target of the disease is the retinal pigmented epithelium (RPE)
18226607To study the molecular mechanisms underlying RPE degeneration, we investigated whether repetitive oxidative stress induced premature senescence in RPE cells from the human ARPE-19 cell line
11381070In 16 of 17 eyes, IGFBP-2 mRNA expression was detected in the RPE
10643311CONCLUSIONS: The feeding of A2-E/LDL complexes to cultured RPE-cells proved to be highly effective in specific loading of the lysosomal compartment, providing a suitable in vitro cell culture model for RPE aging and the investigation of A2-E-effects on lysosomal functions in RPE cells
10576245RPE cells irradiated by near-ultraviolet (NUV) were characterized at cellular, biochemical and molecular levels in order to determine whether light-induced RPE changes contribute to the senescence of RPE cells in vitro
10576245After repeated NUV irradiation, RPE proliferation was markedly suppressed
10576245The phenomena of downregulation of the possible senescence markers imply that photochemical reactions of RPE cells accelerate the process of RPE senescence
10562657Several studies by Burke and others illustrate the relationship between donor age and replicative lifespan, the relationship between geographical location of RPE in the posterior pole and replicative lifespan, and the phenomena of altered cellular morphology and decreased culture saturation density for senescent RPE cells
10562657Our results show that RPE cultures accumulate beta galactosidase positive cells as a function of the number of population doublings and that these data correlate with the shortening of chromosomal telomeres to a functional limit observed for many human cell types at senescence
10562657Basically, the same histochemical procedure is used with a post-staining bleaching step to clearly visualize staining in the RPE
10562657These studies represent a first effort to determine if senescent RPE are present in vivo
669891We have quantitated the content of LPG in human retinal pigment epithelium (RPE) as a function of age
669891The RPE topographic distribution of LPG revealed an increased accumulation in the posterior pole, with a consistent dip at the fovea
669891The ratio of lipofusion accumulation at the posterior pole, to the total RPE, remained constant throughout life
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