MIR1292 Gene

HGNC Family Non-coding RNAs
Name microRNA 1292
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": "\nRenal cell carcinoma (RCC) is a highly aggressive malignancy, and recent studies have implicated the dysregulation of non‐coding RNAs in its progression. In clear cell RCC, a decreased expression of the circular RNA circ‑IP6K2 has been observed, which is clinically associated with advanced tumor stage, higher histological grade, and poorer overall survival. Mechanistic investigations revealed that circ‑IP6K2 normally functions as a molecular sponge for miR‑1292‑5p, thereby curtailing its availability to influence downstream targets."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nmiR‑1292‑5p, when not sequestered by circ‑IP6K2, binds to the 3′ untranslated region of CAMK2N1 mRNA, leading to its downregulation. CAMK2N1 acts as a tumor suppressor by inhibiting the oncogenic β‑catenin/c‑Myc signaling pathway; thus, elevated miR‑1292‑5p activity contributes to enhanced tumor cell proliferation, migration, and invasion."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nTogether, these findings underscore the critical role of miR‑1292‑5p in ccRCC pathogenesis, highlighting that the loss of circ‑IP6K2’s sponging capacity leads to unchecked miR‑1292‑5p activity and suppression of a key tumor suppressor. This miR‑1292‑5p/CAMK2N1 regulatory axis represents a promising avenue for therapeutic intervention in ccRCC."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Jian-Ying Tang, Lu Yang, Qing-Jian Wu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Circ-IP6K2 suppresses tumor progression by modulating the miR-1292-5p/CAMK2N1 signal in clear cell renal cell carcinoma."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Funct Integr Genomics (2024)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s10142-024-01398-9"}], "href": "https://doi.org/10.1007/s10142-024-01398-9"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "38980439"}], "href": "https://pubmed.ncbi.nlm.nih.gov/38980439"}]}]}]}
Synonyms MIRN1292, HSA-MIR-1292, MIR-1292
NCBI Gene ID 100302138
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Predicted Functions View MIR1292's ARCHS4 Predicted Functions.
Co-expressed Genes View MIR1292's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MIR1292's ARCHS4 Predicted Functions.

Functional Associations

MIR1292 has 1,351 functional associations with biological entities spanning 3 categories (molecular profile, cell line, cell type or tissue, gene, protein or microRNA) extracted from 11 datasets.

Click the + buttons to view associations for MIR1292 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 MIR1292 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 MIR1292 gene from the CHEA Transcription Factor Binding Site Profiles dataset.
ChEA Transcription Factor Targets transcription factors binding the promoter of MIR1292 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 MIR1292 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 MIR1292 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 MIR1292 gene from the ENCODE Transcription Factor Binding Site Profiles dataset.
ENCODE Transcription Factor Targets transcription factors binding the promoter of MIR1292 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset.
JASPAR Predicted Transcription Factor Targets transcription factors regulating expression of MIR1292 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 MIR1292 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset.
Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles cell lines with high or low expression of MIR1292 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles dataset.
Roadmap Epigenomics Histone Modification Site Profiles histone modification site profiles with high histone modification abundance at MIR1292 gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset.