MIR888
gene geneOn this page
Also known as hsa-mir-888
Summary
MIR888 (microRNA 888, HGNC:33648) is a microRNA gene on chromosome Xq27.3.
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 100126306 — 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:33648 |
| Approved symbol | MIR888 |
| Name | microRNA 888 |
| Location | Xq27.3 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-mir-888 |
| Ensembl gene | ENSG00000216005 |
| Ensembl biotype | miRNA |
| Entrez | 100126306 |
| RNAcentral | URS000075C9F0 — miRNA, 77 nt, 3 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 miRNA
ENST00000401186
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000401186 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001546530 | 145994784 | 145994860 |
Expression profiles
Bgee: expression breadth broad, 24 present calls, max score 77.57.
Top tissues by expression
24 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| epididymis | UBERON:0001301 | 77.57 | gold quality |
| lung | UBERON:0002048 | 71.31 | gold quality |
| body of stomach | UBERON:0001161 | 67.94 | gold quality |
| skin of leg | UBERON:0001511 | 67.94 | gold quality |
| lower esophagus muscularis layer | UBERON:0035833 | 66.90 | gold quality |
| transverse colon | UBERON:0001157 | 66.26 | gold quality |
| right atrium auricular region | UBERON:0006631 | 64.26 | gold quality |
| subcutaneous adipose tissue | UBERON:0002190 | 64.09 | gold quality |
| esophagogastric junction muscularis propria | UBERON:0035841 | 63.77 | gold quality |
| endocervix | UBERON:0000458 | 63.61 | gold quality |
| Brodmann (1909) area 9 | UBERON:0013540 | 63.55 | gold quality |
| right lobe of thyroid gland | UBERON:0001119 | 63.10 | gold quality |
| caudate nucleus | UBERON:0001873 | 62.91 | gold quality |
| tibial nerve | UBERON:0001323 | 62.64 | gold quality |
| C1 segment of cervical spinal cord | UBERON:0006469 | 62.30 | gold quality |
| muscle layer of sigmoid colon | UBERON:0035805 | 62.19 | gold quality |
| corpus callosum | UBERON:0002336 | 61.41 | gold quality |
| left ovary | UBERON:0002119 | 60.54 | gold quality |
| Ammon’s horn | UBERON:0001954 | 59.99 | gold quality |
| spleen | UBERON:0002106 | 59.22 | gold quality |
| frontal cortex | UBERON:0001870 | 58.89 | gold quality |
| right frontal lobe | UBERON:0002810 | 57.38 | gold quality |
| anterior cingulate cortex | UBERON:0009835 | 54.94 | gold quality |
| hypothalamus | UBERON:0001898 | 39.77 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 1.00 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 10)
- miR-888 functions to promote prostate cancer progression and can suppress protein levels of the tumor suppressor genes RBL1 and SMAD4. (PMID:24200968)
- Over-expression of miR-888 reduced the mRNA levels of E-cadherin in MCF-7 side population sphere cells. (PMID:24480745)
- miR-888 maintains SP properties and regulates EMT and metastasis in MCF-7 cells, potentially by targeting E-Cadherin expression (PMID:24845571)
- miR-888-5p increased the expression of MMP-2 and MMP-9 proteins that promoted cell migration and invasion, and decreased the expression of p53 protein which further enhanced the cell tumorigenicity. (PMID:28337887)
- MiR-888 promotes cell migration and invasion of hepatocellular carcinoma by targeting SMAD4. (PMID:30915745)
- the immunohistochemical results and The Cancer Genome Atlas (TCGA) database revealed that CDC7 was significantly upregulated in lung adenocarcinoma tissues, suggesting that miR888 may function as an oncogene in the progression of lung adenocarcinoma patients, and the miR888/CDC7 axis was not the dominant pathway for CDC7 regulation in patients with lung adenocarcinoma (PMID:31002360)
- Study showed that upregulation of miR-888-3p was associated with idiopathic asthenozoospermia (AZS). This finding paves the way to the future investigation on the actual molecular role of miR-888-3p in aetiology of AZS. (PMID:31012127)
- Circ-CUL2/microRNA-888-5p/RB1CC1 axis participates in cisplatin resistance in NSCLC via repressing cell advancement. (PMID:35068326)
- miR-888 and E-Cadherin Levels in Ductal Carcinoma Breast Cancer as Possible Cancer-Related Markers. (PMID:35442769)
- CircRAD54L2 promotes triple-negative breast cancer progression by regulating the miR-888 family/PDK1 axis. (PMID:36334805)
Cross-species orthologs
0 orthologs
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.