| HGNC Family | Non-coding RNAs |
| Name | microRNA 6133 |
| 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 work has highlighted diverse posttranslational and post‐transcriptional regulatory mechanisms that modulate distinct cellular functions. One study investigated the role of a transmembrane RING domain-containing E3 ubiquitin ligase, RNF167, in neurons, demonstrating that RNF167 facilitates activity-dependent ubiquitination of AMPA receptors and thereby regulates synaptic strength by controlling receptor surface expression. This fine-tuning of excitatory neurotransmission emphasizes the significance of ubiquitin-mediated pathways in synaptic function."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn a separate line of investigation, a screen of human microRNAs capable of suppressing hepatitis B virus replication identified miR-6133-5p as a candidate with potential anti-fibrotic activity. Computational predictions suggest that miR-6133-5p may target several fibrosis-related genes, proposing a mechanism by which this microRNA could mitigate the progression of hepatitis-related liver fibrosis."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nTogether, these studies illustrate the broad spectrum of regulatory systems operating in human cells, from the control of synaptic receptor levels via ubiquitination to the emerging role of specific microRNAs, such as miR-6133-5p, in modulating fibrotic gene expression. Although the two investigations address different biological contexts—neuronal signal modulation versus liver fibrosis—the integration of ubiquitin-mediated protein regulation and microRNA-directed gene silencing underscores the complexity of cellular homeostasis and highlights potential therapeutic targets in both neurological and hepatic diseases."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Marc P Lussier, Bruce E Herring, Yukiko Nasu-Nishimura, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Ubiquitin ligase RNF167 regulates AMPA receptor-mediated synaptic transmission."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Proc Natl Acad Sci U S A (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1073/pnas.1217477109"}], "href": "https://doi.org/10.1073/pnas.1217477109"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23129617"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23129617"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Susumu Hamada-Tsutsumi, Masaya Onishi, Kentaro Matsuura, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Inhibitory Effect of a Human MicroRNA, miR-6133-5p, on the Fibrotic Activity of Hepatic Stellate Cells in Culture."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Int J Mol Sci (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3390/ijms21197251"}], "href": "https://doi.org/10.3390/ijms21197251"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33019495"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33019495"}]}]}]}
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| Synonyms | HSA-MIR-6133 |
| NCBI Gene ID | 102465139 |
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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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MIR6133 has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.
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| Dataset | Summary |
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