MIR4706 Gene

HGNC Family Non-coding RNAs
Name microRNA 4706
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": "\nAlthough the query asks about MIR4706, none of the provided abstracts mention or investigate MIR4706. Instead, these studies focus on the multifaceted biological roles of the dual‐specificity phosphatase DUSP26. Collectively, the data reveal that DUSP26 is a key modulator of diverse signaling cascades that regulate cell identity, survival, inflammation, and metabolism in several disease contexts. For instance, in a type 2 diabetes model, adipsin/C3a signaling was shown to suppress DUSP26 expression in pancreatic beta cells, an effect that helps preserve beta cell identity and function by preventing dedifferentiation and apoptosis."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn oncological settings, DUSP26 functions as a regulatory checkpoint in tumor cell proliferation. One study demonstrated that DUSP26, when stimulated by its binding partner AK2, dephosphorylates key targets such as FADD, thereby inhibiting tumor growth."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": " Similarly, in neuroblastoma, inhibition of DUSP26 activated p53 and p38 MAP kinase tumor-suppressor pathways, leading to decreased tumor cell viability and representing a promising antitumor strategy."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nAdditional investigations have expanded the role of DUSP26 to metabolic and inflammatory disorders. In models of nonalcoholic fatty liver disease, hepatic overexpression of DUSP26 ameliorated steatosis, inflammation, and insulin resistance by interacting with TAK1 and modulating downstream MAPK signaling."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": " Furthermore, in diabetic nephropathy, DUSP26 deficiency was associated with increased renal injury, excessive reactive oxygen species generation, and enhanced TGF-β1–driven fibrosis, thereby suggesting a protective role for DUSP26 in kidney pathology."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "5"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Nicolás Gómez-Banoy, J Sawalla Guseh, Ge Li, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Adipsin preserves beta cells in diabetic mice and associates with protection from type 2 diabetes in humans."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Med (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s41591-019-0610-4"}], "href": "https://doi.org/10.1038/s41591-019-0610-4"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31700183"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31700183"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Hyunjoo Kim, Ho-June Lee, Yumin Oh, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The DUSP26 phosphatase activator adenylate kinase 2 regulates FADD phosphorylation and cell growth."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Commun (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/ncomms4351"}], "href": "https://doi.org/10.1038/ncomms4351"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24548998"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24548998"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Y Shi, I T Ma, R H Patel, et al. "}, {"type": "b", "children": [{"type": "t", "text": "NSC-87877 inhibits DUSP26 function in neuroblastoma resulting in p53-mediated apoptosis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Death Dis (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/cddis.2015.207"}], "href": "https://doi.org/10.1038/cddis.2015.207"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26247726"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26247726"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Ping Ye, Jijun Liu, Wuping Xu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Dual-Specificity Phosphatase 26 Protects Against Nonalcoholic Fatty Liver Disease in Mice Through Transforming Growth Factor Beta-Activated Kinase 1 Suppression."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Hepatology (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/hep.30485"}], "href": "https://doi.org/10.1002/hep.30485"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30582764"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30582764"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Feng Huang, Xu-Xiang Sheng, Hong-Juan Zhang "}, {"type": "b", "children": [{"type": "t", "text": "DUSP26 regulates podocyte oxidative stress and fibrosis in a mouse model with diabetic nephropathy through the mediation of ROS."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochem Biophys Res Commun (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.bbrc.2019.05.032"}], "href": "https://doi.org/10.1016/j.bbrc.2019.05.032"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31155289"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31155289"}]}]}]}
Synonyms MIR-4706
NCBI Gene ID 100616490
API
Download Associations
Predicted Functions View MIR4706's ARCHS4 Predicted Functions.
Co-expressed Genes View MIR4706's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MIR4706's ARCHS4 Predicted Functions.

Functional Associations

MIR4706 has 448 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 MIR4706 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 MIR4706 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 MIR4706 gene from the CHEA Transcription Factor Binding Site Profiles dataset.
ChEA Transcription Factor Targets transcription factors binding the promoter of MIR4706 gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets dataset.
COSMIC Cell Line Gene CNV Profiles cell lines with high or low copy number of MIR4706 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 MIR4706 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 MIR4706 gene from the ENCODE Transcription Factor Binding Site Profiles dataset.
ENCODE Transcription Factor Targets transcription factors binding the promoter of MIR4706 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset.
Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles cell lines with high or low copy number of MIR4706 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 MIR4706 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 MIR4706 gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset.