| HGNC Family | Non-coding RNAs |
| Name | microRNA 1276 |
| 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 studies have underscored the importance of non‐coding RNAs in the regulation of diverse cellular processes. For example, one investigation examined the critical role of the NF‐κB transcription factor in osteoclast differentiation, highlighting complex regulatory networks in cell fate decisions even though miR‐1276 was not directly addressed in this context."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn the field of cancer biology, miR‐1276 has emerged as an important regulatory microRNA that is functionally inactivated through sequestration by oncogenic circular RNAs. In bladder cancer, circ_0002623 is aberrantly upregulated and acts as a competing endogenous RNA by sponging miR‐1276, thereby relieving its inhibition on SMAD2. This cascade not only elevates SMAD2 expression but also modulates downstream TGF‐β and WNT1 signaling pathways to promote cell proliferation, migration, and cell cycle progression."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": " Similarly, in breast cancer, circOMA1 functions in an oncogenic manner by sponging miR‐1276, which results in the upregulation of SIRT4 and contributes to increased tumor cell viability, migration, and invasion."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nAdditional research into circular RNAs in other malignancies, such as gastric cancer, further exemplifies the elaborate nature of circRNA-mediated regulation in tumor progression, although a direct link to miR‐1276 was not delineated in these studies. Together, these findings suggest that miR‐1276 normally functions as a tumor‐suppressive microRNA, and its inactivation via sponging by specific circRNAs may represent a common mechanism contributing to cancer development."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Yandong Zhang, Chengyuan Ma, Chunshui Liu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "NF-κB promotes osteoclast differentiation by overexpressing MITF via down regulating microRNA-1276 expression."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Life Sci (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.lfs.2020.118093"}], "href": "https://doi.org/10.1016/j.lfs.2020.118093"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32673666"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32673666"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Zhaocun Zhang, Haifeng Zhao, Guanwen Zhou, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Circ_0002623 promotes bladder cancer progression by regulating the miR-1276/SMAD2 axis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cancer Sci (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1111/cas.15274"}], "href": "https://doi.org/10.1111/cas.15274"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35048477"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35048477"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Lingli Xu, Ke Xu, Lijun Xiang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Circular RNA OMA1 regulates the progression of breast cancer via modulation of the miR‑1276/SIRT4 axis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Med Rep (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3892/mmr.2021.12367"}], "href": "https://doi.org/10.3892/mmr.2021.12367"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34414449"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34414449"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Xueguang Dong, Xiumei Chen, Yuanhao Zhao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "CircTMEM87A promotes the tumorigenesis of gastric cancer by regulating the miR-1276/SLC7A11 axis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Gastroenterol Hepatol (2024)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1111/jgh.16402"}], "href": "https://doi.org/10.1111/jgh.16402"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "38037531"}], "href": "https://pubmed.ncbi.nlm.nih.gov/38037531"}]}]}]}
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| Synonyms | HSA-MIR-1276, MIR-1276, MIRN1276 |
| NCBI Gene ID | 100302121 |
| API | |
| Download Associations | |
| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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MIR1276 has 295 functional associations with biological entities spanning 3 categories (molecular profile, cell line, cell type or tissue, gene, protein or microRNA) extracted from 13 datasets.
Click the + buttons to view associations for MIR1276 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 MIR1276 gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset. | |
| ChEA Transcription Factor Binding Site Profiles | transcription factor binding site profiles with transcription factor binding evidence at the promoter of MIR1276 gene from the CHEA Transcription Factor Binding Site Profiles dataset. | |
| ChEA Transcription Factor Targets | transcription factors binding the promoter of MIR1276 gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets dataset. | |
| ENCODE Histone Modification Site Profiles | histone modification site profiles with high histone modification abundance at MIR1276 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 MIR1276 gene from the ENCODE Transcription Factor Binding Site Profiles dataset. | |
| ENCODE Transcription Factor Targets | transcription factors binding the promoter of MIR1276 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 MIR1276 gene from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. | |
| GTEx Tissue Gene Expression Profiles | tissues with high or low expression of MIR1276 gene relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset. | |
| JASPAR Predicted Transcription Factor Targets | transcription factors regulating expression of MIR1276 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 MIR1276 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset. | |
| KnockTF Gene Expression Profiles with Transcription Factor Perturbations | transcription factor perturbations changing expression of MIR1276 gene from the KnockTF Gene Expression Profiles with Transcription Factor Perturbations dataset. | |
| MotifMap Predicted Transcription Factor Targets | transcription factors regulating expression of MIR1276 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 MIR1276 gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset. | |