MIR1262 Gene

HGNC Family Non-coding RNAs
Name microRNA 1262
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": "\nmiR‐1262 has emerged as a key regulatory molecule in several disease contexts. In lung cancer, a variant in the miR‐1262 enhancer (rs12740674) was found to reduce miR‐1262 expression via chromosomal looping, with consequent promotion of tumor cell proliferation likely through modulation of downstream targets such as ULK1 and RAB3D."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": " In breast cancer, miR‐1262 acts as a tumor suppressor by negatively regulating LRP8, thereby impairing cell proliferation, clonogenicity, invasion, and migration."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": "\n \nAdditionally, differential expression of miR‐1262 has been implicated in neurological and cardiovascular disorders. In treatment‐resistant schizophrenia, altered miR‐1262 levels in peripheral blood mononuclear cells highlight its potential role in the pathogenesis of the disorder and its value as an early diagnostic biomarker."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": " In the context of sepsis, exosomal hsa‐miR‐1262 from patient serum was shown to target SLC2A1 in myocardial cells; this interaction leads to impaired glycolysis and increased cell apoptosis, thereby contributing to septic myocardial injury."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": "\n \nIn colon cancer, miR‐1262 is downregulated and functions as an antitumor miRNA. Its overexpression directly inhibits fibroblast growth factor receptor 1 (FGFR1), reducing malignant behaviors such as proliferation, invasion, and migration. Moreover, the transcriptional regulation of miR‐1262 by NF‐κB further integrates it into a regulatory axis that modulates colon carcinogenesis."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "5"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Kaipeng Xie, Mengxi Chen, Meng Zhu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A polymorphism in miR-1262 regulatory region confers the risk of lung cancer in Chinese population."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Int J Cancer (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/ijc.30788"}], "href": "https://doi.org/10.1002/ijc.30788"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28510306"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28510306"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Ling Li, Wen-Hui Qu, Hui-Ping Ma, et al. "}, {"type": "b", "children": [{"type": "t", "text": "LRP8, modulated by miR-1262, promotes tumour progression and forecasts the prognosis of patients in breast cancer."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Arch Physiol Biochem (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1080/13813455.2020.1716019"}], "href": "https://doi.org/10.1080/13813455.2020.1716019"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31994910"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31994910"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Xu You, Yunqiao Zhang, Qing Long, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Investigating aberrantly expressed microRNAs in peripheral blood mononuclear cells from patients with treatment‑resistant schizophrenia using miRNA sequencing and integrated bioinformatics."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Med Rep (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3892/mmr.2020.11513"}], "href": "https://doi.org/10.3892/mmr.2020.11513"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33000265"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33000265"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Fangyuan Sun, Huan Geng, Yuxia Sun, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Exosomes derived from the blood of patients with sepsis regulate apoptosis and aerobic glycolysis in human myocardial cells via the hsa‑miR‑1262/SLC2A1 signaling pathway."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Med Rep (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3892/mmr.2022.12635"}], "href": "https://doi.org/10.3892/mmr.2022.12635"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35137927"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35137927"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Weilin Zhang, Zhongcheng Huang, Zhigang Xiao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "NF-κB downstream miR-1262 disturbs colon cancer cell malignant behaviors by targeting FGFR1."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Acta Biochim Biophys Sin (Shanghai) (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3724/abbs.2023235"}], "href": "https://doi.org/10.3724/abbs.2023235"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "37867436"}], "href": "https://pubmed.ncbi.nlm.nih.gov/37867436"}]}]}]}
Synonyms MIRN1262, HSA-MIR-1262, MIR-1262
NCBI Gene ID 100302279
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Predicted Functions View MIR1262's ARCHS4 Predicted Functions.
Co-expressed Genes View MIR1262's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MIR1262's ARCHS4 Predicted Functions.

Functional Associations

MIR1262 has 214 functional associations with biological entities spanning 3 categories (molecular profile, cell line, cell type or tissue, gene, protein or microRNA) extracted from 10 datasets.

Click the + buttons to view associations for MIR1262 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
CCLE Cell Line Gene CNV Profiles cell lines with high or low copy number of MIR1262 gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset.
COSMIC Cell Line Gene CNV Profiles cell lines with high or low copy number of MIR1262 gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset.
ENCODE Histone Modification Site Profiles histone modification site profiles with high histone modification abundance at MIR1262 gene from the ENCODE Histone Modification Site Profiles dataset.
ENCODE Transcription Factor Binding Site Profiles transcription factor binding site profiles with transcription factor binding evidence at the promoter of MIR1262 gene from the ENCODE Transcription Factor Binding Site Profiles dataset.
ENCODE Transcription Factor Targets transcription factors binding the promoter of MIR1262 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset.
GEO Signatures of Differentially Expressed Genes for Gene Perturbations gene perturbations changing expression of MIR1262 gene from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
JASPAR Predicted Transcription Factor Targets transcription factors regulating expression of MIR1262 gene predicted using known transcription factor binding site motifs from the JASPAR Predicted Transcription Factor Targets dataset.
Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles cell lines with high or low copy number of MIR1262 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset.
MotifMap Predicted Transcription Factor Targets transcription factors regulating expression of MIR1262 gene predicted using known transcription factor binding site motifs from the MotifMap Predicted Transcription Factor Targets dataset.
Roadmap Epigenomics Histone Modification Site Profiles histone modification site profiles with high histone modification abundance at MIR1262 gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset.