| HGNC Family | Non-coding RNAs |
| Name | microRNA 571 |
| 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 high‐throughput serum miRNA screenings in patients with chronic liver diseases and type 2 diabetes mellitus (T2DM) have identified miR-571 as one of several miRNAs whose levels are significantly altered. In a study of chronic liver disease and cirrhosis, a systematic screening approach was undertaken to find serum miRNAs with differential expression, suggesting that such molecules, including miR-571, could play a role in modulating disease pathology."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": " Further, serum analyses in T2DM patients, particularly those with microvascular complications and diabetic foot ulcers, revealed that miR-571 is markedly upregulated and correlated with the progression of these complications, indicating its potential utility as a biomarker and risk factor in diabetes-associated vascular injury."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nExperimental evidence has also uncovered a direct functional role for miR-571 in the maintenance of genomic stability. In cancer cells, miR-571 was found to target Geminin—a critical inhibitor of DNA re-replication—thereby reducing Geminin protein levels during late S-phase independently of the anaphase-promoting complex. This regulation of DNA replication and S-phase progression is orchestrated by a Cdk2-c-Myc-miR-571 axis, highlighting its importance in controlling DNA replication and preserving genomic integrity."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn addition to its roles in diabetic complications and genomic stability, miR-571 appears to participate in the progression of liver fibrosis. Elevated in patients with liver fibrosis, miR-571 promotes the activation of human hepatic stellate cells by enhancing proliferation, migration, and inhibiting apoptosis. Mechanistically, increased miR-571 levels upregulate components of the Notch3 signaling pathway—specifically Notch3 and Jagged1—which in turn stimulates fibrogenic processes. These findings suggest that miR-571 not only serves as a potential marker of fibrotic progression but also as a mediator of hepatic stellate cell activation and liver tissue remodeling."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "5"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Christoph Roderburg, Tobias Mollnow, Brenda Bongaerts, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Micro-RNA profiling in human serum reveals compartment-specific roles of miR-571 and miR-652 in liver cirrhosis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PLoS One (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1371/journal.pone.0032999"}], "href": "https://doi.org/10.1371/journal.pone.0032999"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22412969"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22412969"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Cheng Wang, Shujun Wan, Ting Yang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Increased serum microRNAs are closely associated with the presence of microvascular complications in type 2 diabetes mellitus."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Sci Rep (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/srep20032"}], "href": "https://doi.org/10.1038/srep20032"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26831044"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26831044"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Rashin VatanIman, Seyed Hossein Malekpour, Afsoon Afshari, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MiR-770-5p, miR-661 and miR-571 expression level in serum and tissue samples of foot ulcer caused by diabetes mellitus type II in Iranian population."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Biol Rep (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s11033-021-06798-9"}], "href": "https://doi.org/10.1007/s11033-021-06798-9"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34643918"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34643918"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Yi Zhang, Zhuqing Li, Qiang Hao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The Cdk2-c-Myc-miR-571 Axis Regulates DNA Replication and Genomic Stability by Targeting Geminin."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cancer Res (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1158/0008-5472.CAN-19-0020"}], "href": "https://doi.org/10.1158/0008-5472.CAN-19-0020"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31431461"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31431461"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Shuo Cong, Yongmei Liu, Yi Li, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MiR-571 affects the development and progression of liver fibrosis by regulating the Notch3 pathway."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Sci Rep (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s41598-021-00638-3"}], "href": "https://doi.org/10.1038/s41598-021-00638-3"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34750395"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34750395"}]}]}]}
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| Synonyms | HSA-MIR-571, MIRN571 |
| NCBI Gene ID | 693156 |
| 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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MIR571 has 126 functional associations with biological entities spanning 2 categories (functional term, phrase or reference, cell line, cell type or tissue) extracted from 4 datasets.
Click the + buttons to view associations for MIR571 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| GeneRIF Biological Term Annotations | biological terms co-occuring with MIR571 gene in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. | |
| GeneSigDB Published Gene Signatures | PubMedIDs of publications reporting gene signatures containing MIR571 from the GeneSigDB Published Gene Signatures dataset. | |
| GTEx Tissue Gene Expression Profiles | tissues with high or low expression of MIR571 gene relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset. | |
| Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles | cell lines with high or low copy number of MIR571 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset. | |