HCSGD entry for BLVRA


1. General information

Official gene symbolBLVRA
Entrez ID644
Gene full namebiliverdin reductase A
Other gene symbolsBLVR BVR BVRA
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:0004074Biliverdin reductase activityIDAmolecular_function
GO:0005829CytosolTAScellular_component
GO:0006778Porphyrin-containing compound metabolic processTASbiological_process
GO:0008270Zinc ion bindingIEAmolecular_function
GO:0016491Oxidoreductase activityIEAmolecular_function
GO:0042167Heme catabolic processTASbiological_process
GO:0044281Small molecule metabolic processTASbiological_process
GO:0055114Oxidation-reduction processIDAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.98354905590.01146097410.99999024730.2122901478

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

Data sourceUp or downLog fold change
GSE11954Down-0.2150153701
GSE13712_SHEARDown-0.1374805328
GSE13712_STATICUp0.1095972159
GSE19018Down-0.1269549343
GSE19899_A1Down-0.4932021151
GSE19899_A2Down-0.8045317840
PubMed_21979375_A1Down-1.6955385813
PubMed_21979375_A2Down-1.4466684131
GSE35957Down-0.3223087702
GSE36640Down-0.0762182517
GSE54402Down-0.8389870581
GSE9593Up0.0461967347
GSE43922Down-0.5452474917
GSE24585Down-0.0921340473
GSE37065Down-0.1358396249
GSE28863_A1Up0.0317081448
GSE28863_A2Up0.5830713658
GSE28863_A3Down-0.3377420831
GSE28863_A4Up0.0136952802
GSE48662Down-0.1923559831

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Not regulated by compounds

  • Drugs

Name

Drug

Accession number

NADHDB00157 NUTR00041 | DB01907 | EXPT02287 | DB03527

  • MicroRNAs

  • mirTarBase

MiRNA_name

mirBase ID

miRTarBase ID

Experiment

Support type

References (Pubmed ID)

hsa-miR-17-5pMIMAT0000070MIRT050960CLASHFunctional 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: 2 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

22457648In this regard, the biliverdin to bilirubin conversion pathway, via biliverdin reductase (BVR), is suggested to be another major protective mechanism that scavenges lipophilic oxidants because of the lipophilic nature of bilirubin
22457648The efficiency of this bilirubin system might be potentiated by operation of the intertwined bicyclic systems of the suggested redox metabolic cycle of biliverdin and bilirubin and the interactive control cycle of BVR and heme oxygenase
21099244Biliverdin reductase A in the prevention of cellular senescence against oxidative stress
21099244Biliverdin reductase A (BLVRA), an enzyme that converts biliverdin to bilirubin, has recently emerged as a key regulator of the cellular redox cycle
21099244However, the role of BLVRA in the aging process remains unclear
21099244To study the role of BLVRA in the aging process, we compared the stress responses of young and senescent human diploid fibroblasts (HDFs) to the reactive oxygen species (ROS) inducer, hydrogen peroxide (H2O2)
21099244H2O2 markedly induced BLVRA activity in young HDFs, but not in senescent HDFs
21099244Additionally, depletion of BLVRA reduced the H2O2-dependent induction of heme oxygenase-1 (HO-1) in young HDFs, but not in senescent cells, suggesting an aging-dependent differential modulation of responses to oxidative stress
21099244The role of BLVRA in the regulation of cellular senescence was confirmed when lentiviral RNAi- transfected stable primary HDFs with reduced BLVRA expression showed upregulation of the CDK inhibitor family members p16, p53, and p21, followed by cell cycle arrest in G0-G1 phase with high expression of senescence-associated beta-galactosidase
21099244Taken together, these data support the notion that BLVRA contributes significantly to modulation of the aging process by adjusting the cellular oxidative status
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