| HGNC Family | Non-coding RNAs |
| Name | microRNA 1973 |
| 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 research on celiac disease has focused on delineating the molecular underpinnings that contribute to its characteristic immune-mediated and barrier dysfunction features. One study (evaluated in Abstract 1"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "investigated the expression profiles of key pro-inflammatory cytokines (TNF-α, IFN-γ, IL-18) and proteins critical for intestinal tight junction integrity (e.g., Occludin) alongside microRNAs, including miR-122-5p and miR-197-3p, in duodenal biopsies of treated celiac disease patients relative to control subjects.\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn this context, miR-197-3p appears to be a noteworthy regulatory molecule that may be involved in modulating the inflammatory response and maintaining epithelial barrier function. Although the study primarily quantified its expression level rather than detailing its mechanistic role, the observed expression patterns of miR-197-3p in celiac disease suggest that it could influence the balance between pro-inflammatory signaling and the structural integrity of the intestinal epithelium. Altered miR-197-3p levels might therefore contribute to the persistent inflammatory milieu and disrupted tight junction protein expression that are hallmarks of celiac disease pathology."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nCollectively, the findings underscore the potential importance of miR-197-3p as a modulator within the cellular network governing intestinal inflammation and barrier integrity in celiac disease. Further studies are warranted to clarify its precise molecular function and to explore whether targeting miR-197-3p could offer new insights into therapeutic strategies aimed at mitigating immune-mediated tissue damage and restoring proper intestinal function."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Nastaran Asri, Shayan Fallah, Mohammad Rostami-Nejad, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The role of mir-197-3p in regulating the tight junction permeability of celiac disease patients under gluten free diet."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Biol Rep (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s11033-022-08147-w"}], "href": "https://doi.org/10.1007/s11033-022-08147-w"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "36536183"}], "href": "https://pubmed.ncbi.nlm.nih.gov/36536183"}]}]}]}
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| Synonyms | HSA-MIR-1973, MIR-1973 |
| NCBI Gene ID | 100302290 |
| 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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MIR1973 has 225 functional associations with biological entities spanning 3 categories (molecular profile, cell line, cell type or tissue, gene, protein or microRNA) extracted from 9 datasets.
Click the + buttons to view associations for MIR1973 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 MIR1973 gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset. | |
| ChEA Transcription Factor Binding Site Profiles | transcription factor binding site profiles with transcription factor binding evidence at the promoter of MIR1973 gene from the CHEA Transcription Factor Binding Site Profiles dataset. | |
| ChEA Transcription Factor Targets | transcription factors binding the promoter of MIR1973 gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets dataset. | |
| COSMIC Cell Line Gene CNV Profiles | cell lines with high or low copy number of MIR1973 gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset. | |
| ENCODE Histone Modification Site Profiles | histone modification site profiles with high histone modification abundance at MIR1973 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 MIR1973 gene from the ENCODE Transcription Factor Binding Site Profiles dataset. | |
| ENCODE Transcription Factor Targets | transcription factors binding the promoter of MIR1973 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset. | |
| JASPAR Predicted Transcription Factor Targets | transcription factors regulating expression of MIR1973 gene predicted using known transcription factor binding site motifs from the JASPAR Predicted Transcription Factor Targets dataset. | |
| Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles | cell lines with high or low copy number of MIR1973 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset. | |