MIR1273C Gene

HGNC Family Non-coding RNAs
Name microRNA 1273c
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 findings indicate that MIR1273C may function as a molecular regulator linking energy metabolism to cellular activity. In the healthy brain, neurons are the primary site of glucose uptake – a process tightly coordinated with the activity‐dependent enrichment of metabolic enzymes such as hexokinases – suggesting that MIR1273C could modulate gene expression and/or enzyme localization to ensure that neuronal energy demands are met efficiently."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nUnder conditions of chronic stress, where adaptive changes in intracellular nutrient-sensing structures like mitochondria-associated membranes are critical for maintaining energy homoeostasis, MIR1273C is posited to participate in regulating the trafficking of key glycolytic enzymes – potentially safeguarding the coupling between systemic glucose availability and localized cellular metabolism."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nMoreover, broad bioinformatics assessments in sepsis-induced acute lung injury have identified MIR1273C among candidate genes that may influence both inflammatory responses and metabolic dysregulation. This integrated role across diverse physiological and pathological states underscores the emerging view of MIR1273C as a putative post-transcriptional modulator capable of fine-tuning energy metabolism in response to dynamic cellular stress, a finding that invites further mechanistic studies and therapeutic exploration."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}, {"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Iben Lundgaard, Baoman Li, Lulu Xie, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Direct neuronal glucose uptake heralds activity-dependent increases in cerebral metabolism."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Commun (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/ncomms7807"}], "href": "https://doi.org/10.1038/ncomms7807"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25904018"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25904018"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Michael A van der Kooij, Liliana Rojas-Charry, Maryam Givehchi, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Chronic social stress disrupts the intracellular redistribution of brain hexokinase 3 induced by shifts in peripheral glucose levels."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Mol Med (Berl) (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s00109-022-02235-x"}], "href": "https://doi.org/10.1007/s00109-022-02235-x"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35943566"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35943566"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Mingyu Zhu, Xiaokai Tang, Jingjing Xu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Identification of HK3 as a promising immunomodulatory and prognostic target in sepsis-induced acute lung injury."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochem Biophys Res Commun (2024)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.bbrc.2024.149759"}], "href": "https://doi.org/10.1016/j.bbrc.2024.149759"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "38484574"}], "href": "https://pubmed.ncbi.nlm.nih.gov/38484574"}]}]}]}
NCBI Gene ID 100422821
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Predicted Functions View MIR1273C's ARCHS4 Predicted Functions.
Co-expressed Genes View MIR1273C's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MIR1273C's ARCHS4 Predicted Functions.

Functional Associations

MIR1273C has 98 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 MIR1273C 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 MIR1273C gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset.