MIR5705 Gene

Name microRNA 5705
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": "\nA comprehensive review of the provided literature reveals that the studies focus on diverse aspects of cellular metabolism, oncogenesis, and immune responses—involving enzymes such as PYCR1/PYCR2 in proline biosynthesis and their roles in conditions ranging from Cutis Laxa and leukodystrophy to myocardial infarction and cancer progression, as well as on non‐coding RNAs and micropeptides in cancer and asthma."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nNotably, none of the abstracts provide any reference, data, or analysis regarding the function or biological significance of MIR5705. Consequently, while these studies offer insights into metabolic enzymes, signaling pathways, and regulatory non-coding elements in various disease models, they do not address MIR5705, leaving its role undetermined in the contexts examined."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIt follows that further research specifically targeting MIR5705 is required to elucidate its function, any potential regulatory mechanisms it may participate in, and its possible involvement in disease processes. Meanwhile, the current body of work underscores the multifaceted regulation of cellular metabolism and signaling through other molecules, even as the role of MIR5705 remains to be clarified."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "5"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Morgane G Stum, Abigail L D Tadenev, Kevin L Seburn, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Genetic analysis of Pycr1 and Pycr2 in mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Genetics (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/genetics/iyab048"}], "href": "https://doi.org/10.1093/genetics/iyab048"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33734376"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33734376"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Zhuo Li, Ying Jiang, Jian Liu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Exosomes from PYCR1 knockdown bone marrow mesenchymal stem inhibits aerobic glycolysis and the growth of bladder cancer cells via regulation of the EGFR/PI3K/AKT pathway."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Int J Oncol (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3892/ijo.2023.5532"}], "href": "https://doi.org/10.3892/ijo.2023.5532"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "37293856"}], "href": "https://pubmed.ncbi.nlm.nih.gov/37293856"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Sapna Iyer, Min-Jung Park, David Moons, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Clusterin and Pycr1 alterations associate with strain and model differences in susceptibility to experimental pancreatitis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochem Biophys Res Commun (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.bbrc.2016.12.039"}], "href": "https://doi.org/10.1016/j.bbrc.2016.12.039"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27939882"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27939882"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Zhimin Xue, Yiwen Pan, Xugang Kong, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Metabolomic and transcriptomic studies of improvements in myocardial infarction due to Pycr1 deletion."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Mol Med (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1111/jcmm.17637"}], "href": "https://doi.org/10.1111/jcmm.17637"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "36495058"}], "href": "https://pubmed.ncbi.nlm.nih.gov/36495058"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Hong Wang, Dongsheng He "}, {"type": "b", "children": [{"type": "t", "text": "LINC01123 acts as an oncogenic driver in lung adenocarcinoma by regulating the miR-4766-5p/PYCR1 axis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Histol Histopathol (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.14670/HH-18-610"}], "href": "https://doi.org/10.14670/HH-18-610"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "36994814"}], "href": "https://pubmed.ncbi.nlm.nih.gov/36994814"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Zhengxia Wang, Xinyu Jia, Wei Sun, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A micropeptide TREMP encoded by lincR-PPP2R5C promotes Th2 cell differentiation by interacting with PYCR1 in allergic airway inflammation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Allergol Int (2024)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.alit.2024.04.004"}], "href": "https://doi.org/10.1016/j.alit.2024.04.004"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "39025723"}], "href": "https://pubmed.ncbi.nlm.nih.gov/39025723"}]}]}]}
NCBI Gene ID 100847027
API
Download Associations
Predicted Functions View MIR5705's ARCHS4 Predicted Functions.
Co-expressed Genes View MIR5705's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MIR5705's ARCHS4 Predicted Functions.

Functional Associations

MIR5705 has 156 functional associations with biological entities spanning 2 categories (cell line, cell type or tissue, gene, protein or microRNA) extracted from 4 datasets.

Click the + buttons to view associations for MIR5705 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 MIR5705 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 MIR5705 gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset.
Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles cell lines with high or low copy number of MIR5705 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 MIR5705 gene predicted using known transcription factor binding site motifs from the MotifMap Predicted Transcription Factor Targets dataset.