| Name | microRNA 5572 |
| 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 investigations into the molecular underpinnings of sporadic amyotrophic lateral sclerosis (sALS) have revealed that altered microRNA profiles may significantly contribute to disease pathology. In particular, the levels of miR-5572 are notably elevated in the spinal cords of sALS patients, concurrent with a reduction in miR-139-5p, suggesting a dysregulation of miRNA homeostasis in neurodegeneration."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "Dissecting the functional impact of miR-5572, researchers employed bioinformatics tools, notably TargetScan, to predict that SLC30A3, a zinc transporter previously observed at reduced levels in sALS patients, is one of its targets. Experimental validation confirmed that miR-5572 directly regulates SLC30A3 expression, thereby reinforcing the notion that increased miR-5572 may contribute to the diminished SLC30A3 levels seen in sALS."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "Overall, these findings highlight the novel role of miR-5572 as a modulator of SLC30A3, implicating it as a potential key player in sALS pathogenesis. As miR-5572 appears to drive down the expression of a gene essential for zinc homeostasis, its dysregulation might exacerbate neurodegenerative processes, opening avenues for further research into miRNA-based therapeutic strategies in ALS."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Hisaka Kurita, Saori Yabe, Tomoyuki Ueda, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MicroRNA-5572 Is a Novel MicroRNA-Regulating "}, {"type": "a", "children": [{"type": "t", "text": "i"}], "href": "i"}, {"type": "t", "text": "SLC30A3"}, {"type": "a", "children": [{"type": "t", "text": "/i"}], "href": "/i"}, {"type": "t", "text": " in Sporadic Amyotrophic Lateral Sclerosis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Int J Mol Sci (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3390/ijms21124482"}], "href": "https://doi.org/10.3390/ijms21124482"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32599739"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32599739"}]}]}]}
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| NCBI Gene ID | 100847042 |
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| Predicted Functions |
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MIR5572 has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.
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If available, associations are ranked by standardized value
| Dataset | Summary |
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