MIR4255 Gene

HGNC Family Non-coding RNAs
Name microRNA 4255
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": "\nThe study detailed in the provided abstract (PMID"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "focuses on elucidating the role of ARHGEF17 in metastatic lung cancer. ARHGEF17, a Rho guanine nucleotide exchange factor, is shown to integrate signals from the tumor microenvironment, particularly those triggered by lysophosphatidic acid (LPA) through Gi protein–coupled receptors. Upon LPA stimulation, the Gβγ subunit complex promotes ARHGEF17 recruitment to the cell periphery and actin fibers, and relieves its autoinhibitory conformation, thereby enhancing its role in facilitating cell migration and invasion.\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn addition, gene expression analyses indicate that higher levels of ARHGEF17 correlate with reduced survival in patients with advanced-stage lung tumors, underlining its clinical relevance as a driver of tumor growth and metastatic dissemination. Cellular assays further confirm that the activation of ARHGEF17 bolsters the invasive and migratory properties required for metastatic progression (PMID."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIt is important to note that although the query requested a summary concerning MIR4255, the provided abstract (PMID"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "does not mention or provide any details on the function of MIR4255. Thus, based on the available literature in this citation, no information regarding MIR4255’s role in metastatic lung cancer or related pathways was presented. Further investigations or additional sources would be necessary to delineate the function of MIR4255 in this context.\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Irving García-Jiménez, Rodolfo Daniel Cervantes-Villagrana, Jorge Eduardo Del-Río-Robles, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Gβγ mediates activation of Rho guanine nucleotide exchange factor ARHGEF17 that promotes metastatic lung cancer progression."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.jbc.2021.101440"}], "href": "https://doi.org/10.1016/j.jbc.2021.101440"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34808208"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34808208"}]}]}]}
NCBI Gene ID 100422898
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Predicted Functions View MIR4255's ARCHS4 Predicted Functions.
Co-expressed Genes View MIR4255's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MIR4255's ARCHS4 Predicted Functions.

Functional Associations

MIR4255 has 196 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 MIR4255 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 MIR4255 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 MIR4255 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 MIR4255 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 MIR4255 gene from the ENCODE Transcription Factor Binding Site Profiles dataset.
ENCODE Transcription Factor Targets transcription factors binding the promoter of MIR4255 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset.
JASPAR Predicted Transcription Factor Targets transcription factors regulating expression of MIR4255 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 MIR4255 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 MIR4255 gene from the KnockTF Gene Expression Profiles with Transcription Factor Perturbations dataset.
MotifMap Predicted Transcription Factor Targets transcription factors regulating expression of MIR4255 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 MIR4255 gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset.