MIR3667 Gene

HGNC Family Non-coding RNAs
Name microRNA 3667
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
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Across these studies, proteins such as UCP1, UCP2, and particularly UCP3 are shown to modulate mitochondrial proton leak in “mild uncoupling” processes that attenuate reactive oxygen species production, promote fatty acid oxidation, adjust thermogenesis, and protect tissues against lipotoxicity and oxidative stress."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "6"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nMany of the abstracts detail how various hormonal and stress signals—ranging from thyroid hormones and glucocorticoids to reactive oxygen species and fatty acids—regulate uncoupling protein gene expression via transcription factors such as PPARs, Nrf2, and ATF-1. These regulatory cascades adjust mitochondrial bioenergetics in diverse contexts including exercise adaptation, cold exposure, and high-fat feeding."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "7", "end_ref": "12"}]}, {"type": "t", "text": " These studies not only emphasize the dynamic control of energy efficiency and oxidative balance but also suggest multiple levels where post-transcriptional regulation might contribute.\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nGiven that microRNAs are known to fine-tune gene expression, it is plausible to hypothesize that MIR3667—if operative in these contexts—could interface with such signaling networks by targeting transcripts of uncoupling proteins or the regulatory factors that modulate their expression. In doing so, MIR3667 might influence processes such as thermogenesis in brown adipose tissue, protection against ischemia-reperfusion injury in the heart, and the metabolic adaptations during exercise or nutrient excess, as detailed in the literature."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "13", "end_ref": "36"}, {"type": "fg_f", "ref": "31"}, {"type": "fg_f", "ref": "10"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Karim S Echtay, Damien Roussel, Julie St-Pierre, et al. 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"}, {"type": "b", "children": [{"type": "t", "text": "Long-term high-fat feeding induces greater fat storage in mice lacking UCP3."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Am J Physiol Endocrinol Metab (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1152/ajpendo.00779.2007"}], "href": "https://doi.org/10.1152/ajpendo.00779.2007"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18713955"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18713955"}]}, {"type": "r", "ref": 15, "children": [{"type": "t", "text": "Miranda Nabben, Joris Hoeks, Jacob J Briedé, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The effect of UCP3 overexpression on mitochondrial ROS production in skeletal muscle of young versus aged mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "FEBS Lett (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.febslet.2008.11.016"}], "href": "https://doi.org/10.1016/j.febslet.2008.11.016"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19041310"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19041310"}]}, {"type": "r", "ref": 16, "children": [{"type": "t", "text": "Esther Barreiro, Cèlia Garcia-Martínez, Sandra Mas, et al. "}, {"type": "b", "children": [{"type": "t", "text": "UCP3 overexpression neutralizes oxidative stress rather than nitrosative stress in mouse myotubes."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "FEBS Lett (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.febslet.2008.12.023"}], "href": "https://doi.org/10.1016/j.febslet.2008.12.023"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19101552"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19101552"}]}, {"type": "r", "ref": 17, "children": [{"type": "t", "text": "Kari E Wong, Frances L Szeto, Wenshuo Zhang, et al. 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"}, {"type": "b", "children": [{"type": "t", "text": "Isoleucine prevents the accumulation of tissue triglycerides and upregulates the expression of PPARalpha and uncoupling protein in diet-induced obese mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Nutr (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3945/jn.109.108977"}], "href": "https://doi.org/10.3945/jn.109.108977"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20089773"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20089773"}]}, {"type": "r", "ref": 20, "children": [{"type": "t", "text": "Irina G Shabalina, Joris Hoeks, Tatiana V Kramarova, et al. 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"}, {"type": "b", "children": [{"type": "t", "text": "UCP3 translocates lipid hydroperoxide and mediates lipid hydroperoxide-dependent mitochondrial uncoupling."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M110.102699"}], "href": "https://doi.org/10.1074/jbc.M110.102699"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20363757"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20363757"}]}, {"type": "r", "ref": 22, "children": [{"type": "t", "text": "Laurence J Toime, Martin D Brand "}, {"type": "b", "children": [{"type": "t", "text": "Uncoupling protein-3 lowers reactive oxygen species production in isolated mitochondria."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Free Radic Biol Med (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.freeradbiomed.2010.05.010"}], "href": "https://doi.org/10.1016/j.freeradbiomed.2010.05.010"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20493945"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20493945"}]}, {"type": "r", "ref": 23, "children": [{"type": "t", "text": "Ryan J Mailloux, Erin L Seifert, Frédéric Bouillaud, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Glutathionylation acts as a control switch for uncoupling proteins UCP2 and UCP3."}]}, {"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.M111.240242"}], "href": "https://doi.org/10.1074/jbc.M111.240242"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21515686"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21515686"}]}, {"type": "r", "ref": 24, "children": [{"type": "t", "text": "Miranda Nabben, Irina G Shabalina, Esther Moonen-Kornips, et al. 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NCBI Gene ID 100500882
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Predicted Functions View MIR3667's ARCHS4 Predicted Functions.
Co-expressed Genes View MIR3667's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MIR3667's ARCHS4 Predicted Functions.

Functional Associations

MIR3667 has 97 functional associations with biological entities spanning 1 categories (cell line, cell type or tissue) extracted from 1 datasets.

Click the + buttons to view associations for MIR3667 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles cell lines with high or low copy number of MIR3667 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset.