MIR128-1

gene
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Also known as hsa-mir-128ahsa-mir-128-1mir-128-1

Summary

MIR128-1 (microRNA 128-1, HGNC:31510) is a microRNA gene on chromosome 2q21.3.

microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop.

Source: NCBI Gene 406915 — RefSeq curated summary.

At a glance

  • Gene type: non-coding (miRNA) — no protein product; not a drug target. Variant/disease associations are omitted (they would be positional, from an overlapping protein-coding gene).

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:31510
Approved symbolMIR128-1
NamemicroRNA 128-1
Location2q21.3
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-128a, hsa-mir-128-1, mir-128-1
Ensembl geneENSG00000207654
Ensembl biotypemiRNA
OMIM611774
Entrez406915
RNAcentralURS00002D9CBA — miRNA, 82 nt, 29 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000384921

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000384921 — 1 exons

ExonStartEnd
ENSE00001499928135665397135665478

Expression profiles

Bgee: expression breadth broad, 72 present calls, max score 82.73.

Top tissues by expression

72 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
calcaneal tendonUBERON:000370182.73gold quality
monocyteCL:000057679.18gold quality
bloodUBERON:000017876.44gold quality
olfactory segment of nasal mucosaUBERON:000538674.86gold quality
islet of LangerhansUBERON:000000673.78gold quality
gastrocnemiusUBERON:000138873.62gold quality
heartUBERON:000094873.22gold quality
endometriumUBERON:000129572.05gold quality
tibial arteryUBERON:000761071.11gold quality
adult mammalian kidneyUBERON:000008270.94gold quality
lungUBERON:000204870.33gold quality
popliteal arteryUBERON:000225070.24gold quality
stomachUBERON:000094569.51gold quality
prefrontal cortexUBERON:000045168.47gold quality
liverUBERON:000210768.31gold quality
granulocyteCL:000009468.16gold quality
body of stomachUBERON:000116167.37gold quality
lymph nodeUBERON:000002967.11gold quality
left adrenal glandUBERON:000123467.03gold quality
right atrium auricular regionUBERON:000663166.85gold quality
caudate nucleusUBERON:000187366.35gold quality
subcutaneous adipose tissueUBERON:000219066.21gold quality
esophagogastric junction muscularis propriaUBERON:003584166.03gold quality
tonsilUBERON:000237265.96gold quality
ascending aortaUBERON:000149665.85gold quality
Brodmann (1909) area 9UBERON:001354065.68gold quality
left coronary arteryUBERON:000162665.49gold quality
dorsolateral prefrontal cortexUBERON:000983465.28gold quality
lower esophagus muscularis layerUBERON:003583364.77gold quality
esophagus mucosaUBERON:000246964.76gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no0.27

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 40)

  • findings show HIV-1 Tat deregulates expression levels of microRNAs, including mir-128, in cortical neurons; mir-128a inhibits expression of SNAP25; the anti-mir-128a partially restores Tat/mir-128a-induced downregulation of SNAP25 expression (PMID:18381601)
  • a role for miR-128 in the molecular events modulating neuroblastoma progression and aggressiveness (PMID:19713529)
  • miR-128 is a potentially important negative regulator of prostate cancer cell invasion. (PMID:19955085)
  • Data suggest that the hormone-responsive miR-128a can modulate TGFbeta signaling and survival of the letrozole-resistant breast cancer cell lines. (PMID:20054641)
  • Data show there was an inverse correlation between the expression level of EZH2 and that of miR-101 or miR-128a, suggesting that the altered expression of the latter miRNAs accounts for the overexpression of the former. (PMID:21228036)
  • The over-expression of the naturally under-expressed miR-128 in glioma cells resulted in the inhibition of WEE1 in glioblastoma cells. (PMID:21358821)
  • miR-128-1 represses nonsense-mediated RNA decay by targeting the RNA helicase UPF1 and the exon-junction complex core component MLN51. (PMID:21596314)
  • miR-26b and miR-128 as central regulators of pituitary somatomammotrophic tumor growth through activation of the PTEN-AKT pathway. (PMID:22614013)
  • MiR-7 transfection into ovarian cancer cells induces changes in cell adhesion and other developmental networks, while miR-128 transfection induces changes in cell cycle control. (PMID:22853714)
  • Low miR-128 is associated with glioblastoma. (PMID:23482671)
  • MiR-128 exerts pro-apoptotic effect in a p53 transcription-dependent and -independent manner via PUMA-Bak axis. (PMID:23492773)
  • Reduced expression of miR-128 is associated with glioma. (PMID:23835497)
  • Aberrant expression of miR-128 has been detected in many types of human tumors and its validated target genes are involved in cancer-related biological processes such as cell proliferation, differentiation and apoptosis. (PMID:23958464)
  • Low microRNA-128 expression is associated with colorectal cancer. (PMID:24046120)
  • miR-128 inhibition in monocytes from AD patients improves Ab(1-42) degradation. These results could contribute to clarify the molecular mechanisms that affect the imbalanced Ab production/clearance involved in the pathogenesis of AD. (PMID:24064186)
  • CH-11 induced demethylation of the promoter region of miR-128a. (PMID:24316133)
  • The secreted proteins from Salmonella were identified as possible effectors to induce miR-128 expression via the p53 signaling pathway. (PMID:24415783)
  • MIR128a and MIR146a SNPs are associated with diabetic polyneuropathy susceptibility. (PMID:24682535)
  • low expression of miR-124-3p, miR-128-1, and miR-221-3p may constitute a potential marker of astrocytomas that correlates with localization (PMID:24718706)
  • Overexpression of miR-128 increased programmed cell death but had no effect on cell cycle profile (PMID:24846063)
  • Data revealed that upregulated SNAI1 accelerates glioma progression and suppresses the expression of miR-128, which can oppose SNAI1’s effect and modulate SP1 expression. (PMID:24959930)
  • Study showed that the expression of miR-128 and miR-149 was downregulated in glioblastoma; the lower expression of miR-128 and miR-149 contributed to astrocytoma tumorigenesis. (PMID:25017996)
  • miR-128 may act as a promising therapeutic target for improvement of tumor sensitivity to cisplatin. (PMID:25248111)
  • the expression of hsa-miR-128-3p is inversely correlated with the expression of CYP2C9 in hepatocellular carcinoma tumor tissues; the study helped to elucidate the mechanism of CYP2C9 regulation by hsa-miR-128-3p, and the inverse association in hepatocellular carcinoma (PMID:25704921)
  • Data suggest that miR-128 acted as a tumor suppressor inhibiting the head and neck squamous cell carcinoma growth by directly mediating the expression of putative targets. (PMID:25764126)
  • Data indicate that plentiful targets of microRNA miR-128 were screened and laid the foundation for research into the miR-128 regulation network. (PMID:25781272)
  • The use of miR-128 as a diagnostic and/or therapeutic tool may result in improvements in diagnosis, prognosis, and treatment of numerous cancers. (PMID:25916109)
  • miR-128 functions as a tumor suppressor by directly targeting ZEB1 in prostate cancer. (PMID:25921099)
  • we conclude that miR-128-3p, which is frequently downregulated in HCC, inhibits hepatocellular carcinoma (HCC). progression by regulating PIK3R1 and PI3K/AKT activation, and is a prognostic marker for HCC patients. (PMID:25962360)
  • miRNA-128a and its downstream target gene Bmi-1 may have an important role in the radioresistance of U-87 MG glioma cells. (PMID:26238021)
  • Levels of miR-128 are decreased in astrocytoma tumor cell lines compared to normal astrocytes. (PMID:26307612)
  • Mutant IDH1 R132H decreased cell proliferation of U87 glioma cells by inducing the expression of the miRNA miR128a. (PMID:26324126)
  • Decreased expression of miR-128 in both tissue and serum samples of prostate cancer patients may be associated with tumor malignant progression and BCR-free survival. (PMID:26339409)
  • miR-128 represses L1 retrotransposition by binding directly to L1 RNA. (PMID:26367248)
  • miR-27b, miR-101 and miR-128 inhibit angiogenesis by down-regulating VEGF-C expression in gastric cancers. (PMID:26460960)
  • high miR-128 expression suppressed osteosarcoma cell migration, invasion, and EMT development through targeting ITGA2, which may be recommended as a therapeutic target for osteosarcoma (PMID:26700675)
  • miR-128 regulates the differentiation of human hair follicle mesenchymal stem cells into smooth muscle cells via targeting SMAD2, a main transcription regulator in TGF-beta signaling pathway involving smooth muscle cell differentiation. (PMID:27087048)
  • miR-128 and miR-125 could help to increase the nonsense-mutant F9 levels by repressing nonsense-mediated mRNA decay. (PMID:27133073)
  • miR-128a is an up-regulated miRNA in patient with preeclampsia. (PMID:27261578)
  • AurkA suppresses the expression of miR-128, inhibitor of wnt3a mRNA stabilization. (PMID:27341528)

Cross-species orthologs

3 orthologs

OrganismSymbolGene ID
danio_reriomir128-2ENSDARG00000083495
mus_musculusMir128-1ENSMUSG00000065520
rattus_norvegicusMir128-1ENSRNOG00000035534

Paralogs (1): MIR128-2 (ENSG00000207625)

Protein

Non-coding RNA — no protein product; not a drug target.

Function

No curated pathway, Gene-Ontology, or interaction data.

Disease & clinical

No curated disease, variant, or cancer-driver associations.

Drugs & pharmacology

No drug or pharmacology data — not an established drug target.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.