MIR98

gene
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Also known as hsa-mir-98MIRLET7L

Summary

MIR98 (microRNA 98, HGNC:31649) is a microRNA gene on chromosome Xp11.22.

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 407054 — 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:31649
Approved symbolMIR98
NamemicroRNA 98
LocationXp11.22
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-98, MIRLET7L
Ensembl geneENSG00000271886
Ensembl biotypemiRNA
OMIM300810
Entrez407054
RNAcentralURS000075BF40 — miRNA, 119 nt, 8 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000606724

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000606724 — 1 exons

ExonStartEnd
ENSE000036986555355622353556341

Expression profiles

Bgee: expression breadth broad, 61 present calls, max score 86.29.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
olfactory segment of nasal mucosaUBERON:000538686.29gold quality
sural nerveUBERON:001548885.29gold quality
endometriumUBERON:000129578.22gold quality
monocyteCL:000057677.39gold quality
bloodUBERON:000017876.18gold quality
uterusUBERON:000099576.13gold quality
gastrocnemiusUBERON:000138875.19gold quality
adrenal tissueUBERON:001830375.18gold quality
muscle of legUBERON:000138374.89gold quality
bone marrowUBERON:000237173.88gold quality
calcaneal tendonUBERON:000370173.80gold quality
anterior cingulate cortexUBERON:000983571.65gold quality
heart left ventricleUBERON:000208471.00gold quality
adult mammalian kidneyUBERON:000008270.98gold quality
lungUBERON:000204870.35gold quality
stomachUBERON:000094570.09gold quality
heartUBERON:000094869.28gold quality
lower esophagus muscularis layerUBERON:003583368.85gold quality
colonUBERON:000115568.83gold quality
intestineUBERON:000016068.66gold quality
kidneyUBERON:000211368.31gold quality
midbrainUBERON:000189168.27gold quality
substantia nigraUBERON:000203868.27gold quality
right adrenal gland cortexUBERON:003582768.01gold quality
ascending aortaUBERON:000149667.99gold quality
body of pancreasUBERON:000115067.86gold quality
left coronary arteryUBERON:000162667.75gold quality
body of stomachUBERON:000116167.46gold quality
omental fat padUBERON:001041467.29gold quality
esophagogastric junction muscularis propriaUBERON:003584166.93gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no1.20

Regulation

Is transcription factor: no

Upstream regulators (CollecTRI, top): VDR

Literature-anchored findings (GeneRIF, showing 40)

  • miR-98 and let-7 confer cholangiocyte expression of CIS in response to microbial challenge, a process that may be relevant to the regulation of TLR-mediated epithelial innate immune response. (PMID:19592657)
  • These results suggest that the three miRNAs are negative regulators of Fus1 expression in lung cancers. (PMID:19671678)
  • These data suggest that miRNAs play an important role in the regulation of cytokine-inducible Src homology and SOCS expression in epithelial cells in response to C. parvum infection. (PMID:20486857)
  • Study demonstrates that let-7/miR-98 regulated Fas expression and the sensitivity of Fas-mediated apoptosis. (PMID:21228813)
  • Data suggest that miR-98 (and miR-453) down-regulates TP53 expression by targeting the 3-prime-UTR of TP53 in lung cancer cells. (PMID:21880462)
  • miR-98 and miR-181a through their regulatory functions on PGRMC1, PGR, CYP19A1, TIMP3, and DDX3X expression may influence a wide range of endometrial cellular activities during normal menstrual cycle and transition into disease states. (PMID:22492871)
  • MicroRNA-98 and microRNA-214 post-transcriptionally regulate enhancer of zeste homolog 2 and inhibit migration and invasion in human esophageal squamous cell carcinoma. (PMID:22867052)
  • microRNA-98 is a therapeutic target inhibiting prostate cancer growth and a biomarker induced by vitamin D (PMID:23188821)
  • Findings define a regulatory role of miR-98 in tumor angiogenesis and invasion through repressed ALK4 and MMP11 expression. (PMID:23211491)
  • Data indicate that X-linked gene CBL, which downregulates T cell receptor signaling and is decreased in lupus T cells, as a gene targeted by miR-188-3p and miR-98. (PMID:23434382)
  • The findings of this study demonstrate a link between miR-98 expression and the effects of methylprednisolone and provide evidence suggesting that methylprednisolone acts through miR-98 to inhibit specific proinflammatory targets. (PMID:23575983)
  • Our findings newly described RKIP/miR-98 to HMGA2 link and provided a potential mechanism for glioma cell invasion (PMID:24392454)
  • The miR-98 was found highly correlated with breast cancer in formalin-fixed paraffin-embedded tissue (PMID:24696733)
  • Epigallocatechin-3-gallate inhibited the expression of hsa-miR-98-5p, followed by an increase of p53, thus the efficacy of cisplatin was enhanced in NSCLC A549 cells. (PMID:24712372)
  • Our findings suggest that EZH2-specific microRNA-98 can effectively inhibit cell proliferation in vitro and regulate the pRb-E2F pathway in human ovarian cancer (PMID:24771265)
  • miR-98 reduces melanoma metastasis and increases survival in part by reducing IL-6 levels. (PMID:25277211)
  • miR-98 regulates muscle differentiation by altering the expression of the transcription factor E2F5 and, in turn, of multiple E2F5 targets. (PMID:25422988)
  • Specifically, significant down-regulation of the let-7p-5p, miR-98-5p and of miR-183-5p in the study groups (tumor alone and tumor and schizophrenia) was observed (p<0.05). (PMID:25856466)
  • PPARgamma regulates miR-98 to modulate ET-1 expression and pulmonary endothelial cell proliferation in pulmonary hypertension. (PMID:26098770)
  • Findings suggest that down-regulation of miR98 and miR27b promotes CCL18-mediated invasion and migration of breast cancer cells. (PMID:26244871)
  • Renal IRI induces up-regulation of miR-98 dependent on HIF-1alpha, which protects endothelial cells against apoptosis by targeting caspase-3 (PMID:26367177)
  • Overexpression of miR-98 functions as a tumor suppressor in gliomas. (PMID:26502849)
  • These results suggest the downregulation of miR-98 could promote Intervertebral Disc Degeneration through the IL-6/STAT3 signaling pathway. (PMID:26587789)
  • The findings suggest that miR-98 inhibits cancer cell growth and metastasis by direct targeting IGF1R, implicating miR-98 as a novel potential therapeutic target for oral squamous cell carcinoma (OSCC). (PMID:26722410)
  • miR98 was significantly downregulated in HCC tissues and cell lines (PMID:26846175)
  • Study showed that NEAT1 could function as a competing endogenous lncRNA in lung cancer, mediating CTR1 by sponging hsa-mir-98-5p. (PMID:27270317)
  • The inhibition/facilitation of miR-98 expression in myocardial cells can modulate apoptosis. miR-98 was downregulated in the peripheral blood of myocarditis patients. It may interact with the FAS/FASL gene pair to further modulate cell apoptosis. (PMID:27323110)
  • overexpression of miRNA-98 inhibited tumor growth and resistance tolerance by directly binding to the BCL-2 gene. (PMID:27422937)
  • miR-98-5p modulates SNX6 expression and thus plays a critical role in accumulation of Abeta. (PMID:27541017)
  • Data show that miR-98 could inhibit Mecp2 expression by binding the 3’-untranslated region (UTR) of methyl CpG binding protein 2 (Mecp2). (PMID:27573367)
  • Peripheral B cells express less miR-98 in patients with lung cancer.A negative correlation was identified between miR-98 and IL-10 in peripheral B cells. (PMID:27605397)
  • miR-98 may regulate osteogenic differentiation of human bone mesenchymal stromal cells by targeting BMP2. (PMID:27860183)
  • These results suggested that miR-98 functioned as a potential tumor suppressor by regulating Wnt/beta-catenin signal pathway through direct suppression of EZH2 expression and might sever as a potential therapeutic target for HCC patients. (PMID:27890434)
  • miR-98 suppresses IL-10 expression in B cells in the heart, which plays an important role in myocarditis. MiR-98 may be a therapeutic target in the treatment of myocarditis. (PMID:27913008)
  • MicroRNA-98 Suppress Warburg Effect by Targeting HK2 in Colon Cancer Cells. (PMID:28025745)
  • Restored expression of miR-98 attenuated glioma cell invasion and migration. (PMID:28124208)
  • Taken together, these findings indicated that SNHG16 induces breast cancer cell migration by competitively binding miR-98 with E2F5. (PMID:28232182)
  • MiR-98 may act as a tumor suppressor in NSCLC. (PMID:28415380)
  • High miR98 expression is associated with atherosclerosis. (PMID:28436142)
  • Western blotting revealed that overexpression of miR-98 decreased the expression of Col1A1. Overexpression of miR-98 repressed the proliferation of human hypertrophic scar fibroblasts by targeting Col1A1. (PMID:28629444)

Cross-species orthologs

3 orthologs

OrganismSymbolGene ID
danio_reriodre-let-7hENSDARG00000081815
mus_musculusMir98ENSMUSG00000065536
rattus_norvegicusMir98ENSRNOG00000035656

Paralogs (10): MIRLET7E (ENSG00000198972), MIRLET7A2 (ENSG00000198975), MIRLET7C (ENSG00000199030), MIRLET7F1 (ENSG00000199072), MIRLET7D (ENSG00000199133), MIRLET7G (ENSG00000199150), MIRLET7A1 (ENSG00000199165), MIRLET7I (ENSG00000199179), MIRLET7F2 (ENSG00000208012), MIRLET7A3 (ENSG00000283990)

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.

  • Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): Cornelia de Lange syndrome 2