| HGNC Family | Non-coding RNAs |
| Name | microRNA 7847 |
| 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": "\nStudies have recently elucidated a novel role for miR‑7847‑3p as a key regulator within a competing endogenous RNA network that modulates inflammatory signaling during sepsis. Specifically, miR‑7847‑3p functions by binding to and suppressing expression of protein kinase C gamma (PRKCG), a critical effector within the MAPK cascade. In immune cells exposed to lipopolysaccharide (LPS), the long noncoding RNA IL‑17RA‑1 sequesters miR‑7847‑3p, thereby decreasing its availability and relieving its repression on PRKCG. This de-repression enables enhanced activation of downstream MAPK signaling components (evidenced by increased levels of phosphorylated MEKK1 and JNK), which in turn elevates proinflammatory responses, affecting cell viability and migration. These findings suggest that miR‑7847‑3p normally acts as an anti-inflammatory modulator by targeting PRKCG, and its sequestration via IL‑17RA‑1 contributes to an exacerbated sepsis response."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Yuanxiu Gan, Jie Long, Yan Zeng, et al. "}, {"type": "b", "children": [{"type": "t", "text": "lncRNA IL-17RA-1 Attenuates LPS-Induced Sepsis via miR-7847-3p/PRKCG-Mediated MAPK Signaling Pathway."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mediators Inflamm (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1155/2022/9923204"}], "href": "https://doi.org/10.1155/2022/9923204"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "36274974"}], "href": "https://pubmed.ncbi.nlm.nih.gov/36274974"}]}]}]}
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| Synonyms | HSA-MIR-7847 |
| NCBI Gene ID | 102465993 |
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| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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MIR7847 has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.
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| Dataset | Summary |
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