MIR522
gene geneOn this page
Also known as hsa-mir-522
Summary
MIR522 (microRNA 522, HGNC:32127) is a microRNA gene on chromosome 19q13.42.
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 574495 — 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
| Field | Value |
|---|---|
| HGNC ID | HGNC:32127 |
| Approved symbol | MIR522 |
| Name | microRNA 522 |
| Location | 19q13.42 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-mir-522 |
| Ensembl gene | ENSG00000283685 |
| Ensembl biotype | miRNA |
| OMIM | 620623 |
| Entrez | 574495 |
| RNAcentral | URS0000680AAF — miRNA, 87 nt, 7 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 miRNA
ENST00000385071
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000385071 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001806829 | 53751211 | 53751297 |
Expression profiles
Bgee: expression breadth tissue_specific, 8 present calls, max score 73.11.
Top tissues by expression
8 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| monocyte | CL:0000576 | 73.11 | gold quality |
| blood | UBERON:0000178 | 68.15 | gold quality |
| body of pancreas | UBERON:0001150 | 66.70 | gold quality |
| transverse colon | UBERON:0001157 | 64.49 | gold quality |
| thoracic mammary gland | UBERON:0005200 | 62.86 | gold quality |
| omental fat pad | UBERON:0010414 | 61.61 | gold quality |
| lower esophagus muscularis layer | UBERON:0035833 | 60.56 | gold quality |
| left testis | UBERON:0004533 | 46.71 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.82 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 14)
- These results suggest variation at the PLIN4 locus, and its interaction with PUFA as a modulator of obesity related phenotypes, acts in part through creation of a miR-522 regulatory site (PMID:21533135)
- miR-522 regulates cell proliferation, detachment, migration, and epithelial-mesenchymal transition. (PMID:25131211)
- Glioblastoma tumor cell proliferation was promoted through miR-522. (PMID:25776496)
- MiR522 was overexpressed in the HT29/DOX cells, the protein expression levels of ABCB5 were downregulated. (PMID:26043974)
- DKK1 (dickkopf-1) and SFRP2 (secreted frizzled-related protein 2) were the targets of miR-522 in hepatocellular carcinoma (PMID:26960688)
- The data indicate that HMGB1-miR-522-3p-PTGR1 axis may be involved in the abnormal resolution of inflammation and suggest that this mechanism might be a target for modulation of chronic inflammatory disorder. (PMID:28088550)
- Results suggested that miR-522 regulated the expression of proinflammatory cytokines and MMPs partly via targeting SOCS3 in RA synovial fibroblasts, which may contribute to pathogenesis of RA. (PMID:29394098)
- Long non-coding RNA HCG11 sponging miR-522-3p inhibits the tumorigenesis of non-small cell lung cancer by upregulating SOCS5. (PMID:32844573)
- Targeting of DeltaNp63alpha by miR-522 promotes the migration of breast epithelial cells. (PMID:33369228)
- MicroRNA-522-3p plays an oncogenic role in glioblastoma through activating Wnt/beta-catenin signaling pathway via targeting SFRP2. (PMID:33395185)
- miR-522 regulates cell proliferation, migration, invasion capacities and acts as a potential biomarker to predict prognosis in triple-negative breast cancer. (PMID:34518949)
- rs6426881 in the 3’-UTR of PBX1 is involved in breast and gastric cancers via altering the binding potential of miR-522-3p. (PMID:34655407)
- LncRNA DHRS4-AS1 ameliorates hepatocellular carcinoma by suppressing proliferation and promoting apoptosis via miR-522-3p/SOCS5 axis. (PMID:34666613)
- Long noncoding RNA LINC00238 suppresses the malignant phenotype of liver cancer by sponging miR522. (PMID:35014686)
Cross-species orthologs
0 orthologs
Paralogs (24): MIR520E (ENSG00000207599), MIR515-2 (ENSG00000207615), MIR515-1 (ENSG00000207616), MIR516A2 (ENSG00000207620), MIR526A1 (ENSG00000207629), MIR521-1 (ENSG00000207634), MIR518F (ENSG00000207706), MIR525 (ENSG00000207711), MIR520B (ENSG00000207722), MIR517A (ENSG00000207734), MIR520C (ENSG00000207738), MIR516A1 (ENSG00000207767), MIR519C (ENSG00000207788), MIR519B (ENSG00000207825), MIR517B (ENSG00000207837), MIR518B (ENSG00000207862), MIR516B1 (ENSG00000207946), MIR518E (ENSG00000207987), MIR524 (ENSG00000283289), MIR518D (ENSG00000283330), MIR523 (ENSG00000283455), MIR518C (ENSG00000283490), MIR520F (ENSG00000283540), MIR519A2 (ENSG00000284362)
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.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.