| HGNC Family | Non-coding RNAs |
| Name | microRNA 8068 |
| 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 current body of work on vascular integrity and endothelial function, as illustrated by studies on cerebral cavernous malformations (CCMs) and atherosclerosis, emphasizes key protein signaling pathways, yet neither investigation provides direct insights regarding the function of MIR8068. In the study focusing on CCMs, endothelial cell–specific mechanisms regulated via HEG1‑CCM protein interactions were delineated as critical for proper vascular development and integrity."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nSimilarly, research exploring the protective effects of stable blood flow against atherosclerosis implicated hemodynamic forces in modulating endothelial responses; however, this work does not describe any role for MIR8068 in these processes."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn summary, while these investigations provide important insights into endothelial signaling and vascular disease mechanisms, none of the presented abstracts address or characterize MIR8068. Consequently, the specific biological function of MIR8068 in vascular development or pathology remains unestablished, highlighting an area for future study.\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Benjamin Kleaveland, Xiangjian Zheng, Jian J Liu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Regulation of cardiovascular development and integrity by the heart of glass-cerebral cavernous malformation protein pathway."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Med (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/nm.1918"}], "href": "https://doi.org/10.1038/nm.1918"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19151727"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19151727"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Ian A Tamargo, Kyung In Baek, Chenbo Xu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "HEG1 Protects Against Atherosclerosis by Regulating Stable Flow-Induced KLF2/4 Expression in Endothelial Cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Circulation (2024)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1161/CIRCULATIONAHA.123.064735"}], "href": "https://doi.org/10.1161/CIRCULATIONAHA.123.064735"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "38099436"}], "href": "https://pubmed.ncbi.nlm.nih.gov/38099436"}]}]}]}
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| Synonyms | HSA-MIR-8068 |
| NCBI Gene ID | 102466876 |
| API | |
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| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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MIR8068 has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.
Click the + buttons to view associations for MIR8068 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary |
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