| HGNC Family | Non-coding RNAs |
| Name | microRNA 219b |
| Description | 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. [provided by RefSeq, Sep 2009] |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nRecent evidence underscores a growing appreciation for the diversity of regulatory mechanisms orchestrating specialized cellular functions. Studies investigating dual‐specificity tyrosine‐phosphorylated and regulated kinases have revealed complex patterns of tissue‐specific splicing and activity that contribute to signaling diversity during cell differentiation and survival."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": " Although these reports focus primarily on kinase isoforms, they set the stage for understanding how additional layers of regulation—such as post‐transcriptional control by microRNAs—integrate into these signaling networks.\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn the context of the central nervous system, emerging studies indicate that MIR219B (often detected as miR-219 or its mature form miR-219-5p) plays a critical inhibitory role in excitatory neurotransmission. In patients with mesial temporal lobe epilepsy, an inverse relationship was observed between miR-219 levels and the expression of the NMDA receptor subunit NR1 in both the hippocampus and amygdala. These data suggest that MIR219B normally acts to restrain NMDA receptor–mediated excitatory signaling, and its dysregulation may contribute to epileptogenesis."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nAdditional work in non‐neuronal tissue highlights another facet of MIR219B function. In studies examining wound healing, miR-219-5p was found to target TMEM98 in keratinocytes, thereby inhibiting cell proliferation and migration—processes essential for effective wound closure. This observation broadens the biological significance of MIR219B, suggesting that through its capacity to modulate gene expression, it may influence both neural excitability and tissue repair."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "F Sacher, C Möller, W Bone, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The expression of the testis-specific Dyrk4 kinase is highly restricted to step 8 spermatids but is not required for male fertility in mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell Endocrinol (2007)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.mce.2006.12.041"}], "href": "https://doi.org/10.1016/j.mce.2006.12.041"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17292540"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17292540"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Chrisovalantis Papadopoulos, Krisztina Arato, Eva Lilienthal, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Splice variants of the dual specificity tyrosine phosphorylation-regulated kinase 4 (DYRK4) differ in their subcellular localization and catalytic activity."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M110.157909"}], "href": "https://doi.org/10.1074/jbc.M110.157909"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21127067"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21127067"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Osmi Hamamoto, Daniela Pretti da Cunha Tirapelli, Fermino Sanches Lizarte Neto, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Modulation of NMDA receptor by miR-219 in the amygdala and hippocampus of patients with mesial temporal lobe epilepsy."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Clin Neurosci (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.jocn.2020.02.024"}], "href": "https://doi.org/10.1016/j.jocn.2020.02.024"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32111564"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32111564"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Q Tang, H Ran "}, {"type": "b", "children": [{"type": "t", "text": "MicroRNA-219-5p inhibits wound healing by targeting TMEM98 in keratinocytes under normoxia and hypoxia condition."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Eur Rev Med Pharmacol Sci (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.26355/eurrev_201810_16026"}], "href": "https://doi.org/10.26355/eurrev_201810_16026"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30338788"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30338788"}]}]}]}
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| Synonyms | HSA-MIR-219B, MIR2964A, MIR-219B |
| NCBI Gene ID | 100616335 |
| API | |
| Download Associations | |
| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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MIR219B has 328 functional associations with biological entities spanning 3 categories (molecular profile, cell line, cell type or tissue, gene, protein or microRNA) extracted from 6 datasets.
Click the + buttons to view associations for MIR219B from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| CCLE Cell Line Gene CNV Profiles | cell lines with high or low copy number of MIR219B gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset. | |
| ENCODE Histone Modification Site Profiles | histone modification site profiles with high histone modification abundance at MIR219B gene from the ENCODE Histone Modification Site Profiles dataset. | |
| ENCODE Transcription Factor Binding Site Profiles | transcription factor binding site profiles with transcription factor binding evidence at the promoter of MIR219B gene from the ENCODE Transcription Factor Binding Site Profiles dataset. | |
| ENCODE Transcription Factor Targets | transcription factors binding the promoter of MIR219B gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset. | |
| Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles | cell lines with high or low copy number of MIR219B gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset. | |
| Roadmap Epigenomics Histone Modification Site Profiles | histone modification site profiles with high histone modification abundance at MIR219B gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset. | |