| HGNC Family | Non-coding RNAs |
| Name | microRNA 6715b |
| 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": "\nMIR6715B appears to be a candidate noncoding RNA implicated in the genetic etiology of diseases such as primary ovarian insufficiency (POI). In studies focused on POI (1), its genomic region was highlighted in efforts to uncover the largely unknown genetic basis of this female infertility disorder, suggesting that MIR6715B may be involved in ovarian development or function."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "MIR6715B is also discussed in the context of RNA transcription regulation. In gene expression analyses investigating the diurnal regulation of RNA polymerase III (Pol III)‐dependent transcription (2), the interplay between nutrient signals and circadian clock mechanisms was shown to govern the transcriptional output of small noncoding RNAs. Although MIR6715B is a microRNA, its potential regulatory roles may intersect with the dynamic modulation of transcription as cells anticipate and respond to metabolic cues, placing it among transcripts whose accumulation is finely tuned by both feeding and internal circadian signals."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": "Furthermore, investigations into liver regeneration after partial hepatectomy (3) have revealed that Pol III transcription adapts to increased cellular proliferation by modulating the occupancy of target genes, including those encoding various noncoding RNAs. In this regenerative setting, MIR6715B may represent one of the responsive noncoding elements that integrates transcriptional adaptations to meet the heightened demands of cellular growth and division."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": ""}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Monica M Franca, Xingfa Han, Mariana F A Funari, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Exome Sequencing Reveals the POLR3H Gene as a Novel Cause of Primary Ovarian Insufficiency."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Clin Endocrinol Metab (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1210/jc.2018-02485"}], "href": "https://doi.org/10.1210/jc.2018-02485"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30830215"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30830215"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "François Mange, Viviane Praz, Eugenia Migliavacca, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Diurnal regulation of RNA polymerase III transcription is under the control of both the feeding-fasting response and the circadian clock."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Genome Res (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1101/gr.217521.116"}], "href": "https://doi.org/10.1101/gr.217521.116"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28341772"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28341772"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Meghdad Yeganeh, Viviane Praz, Cristian Carmeli, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Differential regulation of RNA polymerase III genes during liver regeneration."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nucleic Acids Res (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/nar/gky1282"}], "href": "https://doi.org/10.1093/nar/gky1282"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30597109"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30597109"}]}]}]}
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| Synonyms | HSA-MIR-6715B |
| NCBI Gene ID | 102465427 |
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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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MIR6715B has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.
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| Dataset | Summary |
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