HCSGD entry for MKRN1


1. General information

Official gene symbolMKRN1
Entrez ID23608
Gene full namemakorin ring finger protein 1
Other gene symbolsRNF61
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:0003674Molecular_functionNDmolecular_function
GO:0003682Chromatin bindingIEAmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005575Cellular_componentNDcellular_component
GO:0008150Biological_processNDbiological_process
GO:0008270Zinc ion bindingIEAmolecular_function
GO:0016567Protein ubiquitinationIEAbiological_process
GO:0016874Ligase activityIEAmolecular_function
GO:0046872Metal ion bindingIEAmolecular_function
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.09348240570.94186087530.64076833331.0000000000

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

Data sourceUp or downLog fold change
GSE11954Up0.0758638787
GSE13712_SHEARDown-0.0716595721
GSE13712_STATICUp0.0029294269
GSE19018Up0.8021532336
GSE19899_A1Up0.2071472704
GSE19899_A2Up0.3555161945
PubMed_21979375_A1Up0.1503453704
PubMed_21979375_A2Up0.3939147545
GSE35957Down-0.1465550232
GSE36640Up0.1119274964
GSE54402Down-0.0918275370
GSE9593Up0.2315422902
GSE43922Down-0.0215340868
GSE24585Up0.4994811527
GSE37065Up0.2825955332
GSE28863_A1Down-0.0255928329
GSE28863_A2Up0.1573942607
GSE28863_A3Up0.0261322059
GSE28863_A4Down-0.1422892228
GSE48662Up0.1725709819

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-373-3pMIMAT0000726MIRT002511MicroarrayFunctional MTI (Weak)15685193
hsa-miR-375MIMAT0000728MIRT019801MicroarrayFunctional MTI (Weak)20215506
hsa-miR-574-3pMIMAT0003239MIRT040519CLASHFunctional MTI (Weak)23622248
hsa-miR-197-3pMIMAT0000227MIRT048130CLASHFunctional MTI (Weak)23622248
hsa-let-7c-5pMIMAT0000064MIRT051838CLASHFunctional MTI (Weak)23622248
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  • mirRecord

MicroRNA name

mirBase ID

Target site number

MiRNA mature ID

Test method inter

MiRNA regulation site

Reporter target site

Pubmed ID

hsa-miR-373-3pMIMAT0000726NAhsa-miR-37315685193
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6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 1 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

23104211BACKGROUND: We investigated whether Makorin ring finger protein 1 (MKRN1), an E3 ligase, affects p14ARF-associated cellular senescence and tumorigenesis by posttranslational modification in gastric tumorigenesis
23104211METHODS: A link between MKRN1 and ARF was examined in MKRN1 null mouse embryonic fibroblasts (MEFs) and in human fibroblasts and gastric cancer cells by silencing MKRN1 using small interfering RNA (siRNA) and short hairpin RNA (shRNA)
23104211Ubiquitination and proteasomal degradation assays were used to assess p14ARF degradation associated with MKRN1
23104211MKRN1 and p14ARF expression levels were analyzed with immunohistochemistry in malignant and normal tissues from gastric cancer patients and with chi(2) tests
23104211The tumor growth of gastric cancer cells stably expressing MKRN1 shRNA, p14ARF shRNA, or both was examined in mouse xenograft models (n = 4-6) and analyzed with unpaired t tests
23104211RESULTS: MKRN1 knockout MEFs exhibited premature senescence and growth retardation with increased p19ARF protein expression
23104211Similar results were obtained for human fibroblasts or gastric cancer cell lines by MKRN1 knockdown
23104211Biochemical analyses confirmed that MKRN1 targets p14ARF for ubiquitination and subsequent proteasome-dependent degradation
23104211A statistically significant association was shown between MKRN1 overexpression and p14ARF underexpression (P =
23104211Xenograft analyses using p53-functional AGS or -dysfunctional SNU601 cells displayed statistically significant tumor growth retardation by silencing MKRN1, which was reversed under depletion of p14ARF (AGS cells, MKRN1 knockdown tumors vs MKRN1 and p14ARF knockdown tumors: 164
23104211CONCLUSIONS: We demonstrated that MKRN1 functions as a novel E3 ligase of p14ARF and that it potentially regulates cellular senescence and tumorigenesis in gastric cancer
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