| HGNC Family | Non-coding RNAs |
| Name | microRNA 6747 |
| 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": "\nThe studies collectively highlight that MIR6747, whose function appears intertwined with the activities of procolipase and its derived peptide enterostatin, plays an essential regulatory role in lipid digestion and energy homeostasis. In a mouse model lacking procolipase, the enzyme’s absence resulted in fat malabsorption on a high‐fat diet, impaired neonatal weight gain, and compensatory hyperphagia—all underscoring its critical function in fat digestion and in establishing a physiological body weight set point during early development."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "Disruption of normal gene regulation associated with MIR6747 was also observed in liver metabolic pathways where increased expression of procolipase, alongside the pancreatic-related protein 2, was linked to epigenetic modifications that enhance retinyl ester hydrolysis. Such regulation appears sensitive to changes in the S-adenosylmethionine/S-adenosylhomocysteine ratio, light exposure, and vitamin A signaling, indicating a broader role that extends into modulation of hepatic vitamin A metabolism."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": "Furthermore, the release of the pentapeptide enterostatin from procolipase has been shown to contribute to developmental survival and lipid metabolism. Although enterostatin is not indispensable for controlling dietary fat intake or overall growth, its absence or replacement alters serum cholesterol profiles, and its administration in neonatal models of procolipase deficiency significantly improves survival. This suggests that MIR6747—via its precursor procolipase and cleavage product enterostatin—not only supports efficient fat digestion, but it may also influence cholesterol balance and developmental maturation."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": ""}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Dymphna D'Agostino, Richard A Cordle, John Kullman, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Decreased postnatal survival and altered body weight regulation in procolipase-deficient mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2002)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M108328200"}], "href": "https://doi.org/10.1074/jbc.M108328200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "11751900"}], "href": "https://pubmed.ncbi.nlm.nih.gov/11751900"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Wenqiang Pang, Ying Zhang, Shiming Wang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The mPlrp2 and mClps genes are involved in the hydrolysis of retinyl esters in the mouse liver."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Lipid Res (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1194/jlr.M010082"}], "href": "https://doi.org/10.1194/jlr.M010082"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21339507"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21339507"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Rita Miller, Dymphna D'Agostino, Charlotte Erlanson-Albertsson, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Enterostatin deficiency increases serum cholesterol but does not influence growth and food intake in mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Am J Physiol Endocrinol Metab (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1152/ajpendo.91008.2008"}], "href": "https://doi.org/10.1152/ajpendo.91008.2008"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19622781"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19622781"}]}]}]}
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| Synonyms | HSA-MIR-6747 |
| NCBI Gene ID | 102465447 |
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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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MIR6747 has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.
Click the + buttons to view associations for MIR6747 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary |
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