| HGNC Family | Non-coding RNAs |
| Name | microRNA 8077 |
| 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": "\nAlthough none of the provided abstracts explicitly mention MIR8077, they collectively illuminate the multifaceted roles of MECP2—an essential methyl‐CpG binding protein whose precise dosage is critical for normal neurodevelopment. In these studies, MECP2 is shown to act as both a transcriptional repressor and activator, orchestrating large‐scale gene expression programs in key brain regions. These regulatory actions, which include direct promoter binding, recruitment of chromatin‐modifying enzymes, and interactions with activity‐dependent signaling cascades, underlie its involvement in neuronal maturation, synaptic plasticity, and neuropsychiatric disease states such as Rett syndrome."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "7"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nA set of these abstracts further emphasizes how perturbations in MECP2 levels profoundly impact synaptic function and neuronal connectivity. In particular, altered MECP2 dosage is linked to changes in excitatory and inhibitory neurotransmission, synaptic protein expression, and the structural maturation of dendrites and spines. In addition, several studies highlight a role for microRNAs—including miR-137, miR-22, and miR-132—in modulating neuronal gene expression and plasticity via post‐transcriptional repression of key targets such as MECP2 and its downstream effectors. These findings underscore a broader regulatory network in which microRNAs fine-tune chromatin and synaptic dynamics."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "8", "end_ref": "14"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nBy analogy with other microRNAs that regulate MECP2-dependent pathways, it is reasonable to hypothesize that MIR8077—although not directly addressed in these studies—may serve as an additional layer of post-transcriptional control within this intricate network. In other words, MIR8077 could be involved in fine-tuning MECP2 expression or modulating its downstream targets, thereby participating in the regulation of neuronal differentiation, synaptic homeostasis, and activity-dependent gene expression. This conjecture is supported by a wealth of data from related studies that explore epigenetic regulation, neural circuit maturation, and the interplay between microRNAs and transcriptional programs implicated in neurodevelopmental disorders."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "15", "end_ref": "40"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "R Z Chen, S Akbarian, M Tudor, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Genet (2001)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/85906"}], "href": "https://doi.org/10.1038/85906"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "11242118"}], "href": "https://pubmed.ncbi.nlm.nih.gov/11242118"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Mona Shahbazian, Juan Young, Lisa Yuva-Paylor, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Neuron (2002)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/s0896-6273(02)00768-7"}], "href": "https://doi.org/10.1016/s0896-6273(02"}, {"type": "t", "text": "00768-7) PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12160743"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12160743"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Francois Fuks, Paul J Hurd, Daniel Wolf, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The methyl-CpG-binding protein MeCP2 links DNA methylation to histone methylation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2003)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M210256200"}], "href": "https://doi.org/10.1074/jbc.M210256200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12427740"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12427740"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Wen G Chen, Qiang Chang, Yingxi Lin, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Derepression of BDNF transcription involves calcium-dependent phosphorylation of MeCP2."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Science (2003)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1126/science.1086446"}], "href": "https://doi.org/10.1126/science.1086446"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "14593183"}], "href": "https://pubmed.ncbi.nlm.nih.gov/14593183"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Hsiao-Tuan Chao, Hongmei Chen, Rodney C Samaco, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nature (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/nature09582"}], "href": "https://doi.org/10.1038/nature09582"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21068835"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21068835"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Marian Mellén, Pinar Ayata, Scott Dewell, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MeCP2 binds to 5hmC enriched within active genes and accessible chromatin in the nervous system."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.cell.2012.11.022"}], "href": "https://doi.org/10.1016/j.cell.2012.11.022"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23260135"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23260135"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Maria Chahrour, Sung Yun Jung, Chad Shaw, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MeCP2, a key contributor to neurological disease, activates and represses transcription."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Science (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1126/science.1153252"}], "href": "https://doi.org/10.1126/science.1153252"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18511691"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18511691"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Peter J Skene, Robert S Illingworth, Shaun Webb, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Neuronal MeCP2 is expressed at near histone-octamer levels and globally alters the chromatin state."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.molcel.2010.01.030"}], "href": "https://doi.org/10.1016/j.molcel.2010.01.030"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20188665"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20188665"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Ann L Collins, Jonathan M Levenson, Alexander P Vilaythong, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Mild overexpression of MeCP2 causes a progressive neurological disorder in mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Hum Mol Genet (2004)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/hmg/ddh282"}], "href": "https://doi.org/10.1093/hmg/ddh282"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "15351775"}], "href": "https://pubmed.ncbi.nlm.nih.gov/15351775"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Alysson R Muotri, Maria C N Marchetto, Nicole G Coufal, et al. 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"}, {"type": "b", "children": [{"type": "t", "text": "Ischemic preconditioning potentiates the protective effect of stem cells through secretion of exosomes by targeting Mecp2 via miR-22."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PLoS One (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1371/journal.pone.0088685"}], "href": "https://doi.org/10.1371/journal.pone.0088685"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24558412"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24558412"}]}, {"type": "r", "ref": 12, "children": [{"type": "t", "text": "Nurit Ballas, Daniel T Lioy, Christopher Grunseich, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Neurosci (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/nn.2275"}], "href": "https://doi.org/10.1038/nn.2275"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19234456"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19234456"}]}, {"type": "r", "ref": 13, "children": [{"type": "t", "text": "Juan I Young, Eugene P Hong, John C Castle, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Proc Natl Acad Sci U S A (2005)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1073/pnas.0507856102"}], "href": "https://doi.org/10.1073/pnas.0507856102"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "16251272"}], "href": "https://pubmed.ncbi.nlm.nih.gov/16251272"}]}, {"type": "r", "ref": 14, "children": [{"type": "t", "text": "Noriyuki Kishi, Jeffrey D Macklis "}, {"type": "b", "children": [{"type": "t", "text": "MECP2 is progressively expressed in post-migratory neurons and is involved in neuronal maturation rather than cell fate decisions."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell Neurosci (2004)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.mcn.2004.07.006"}], "href": "https://doi.org/10.1016/j.mcn.2004.07.006"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "15519245"}], "href": "https://pubmed.ncbi.nlm.nih.gov/15519245"}]}, {"type": "r", "ref": 15, "children": [{"type": "t", "text": "Jelena Mann, David C K Chu, Aidan Maxwell, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MeCP2 controls an epigenetic pathway that promotes myofibroblast transdifferentiation and fibrosis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Gastroenterology (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1053/j.gastro.2009.10.002"}], "href": "https://doi.org/10.1053/j.gastro.2009.10.002"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19843474"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19843474"}]}, {"type": "r", "ref": 16, "children": [{"type": "t", "text": "Sandra Luikenhuis, Emanuela Giacometti, Caroline F Beard, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Proc Natl Acad Sci U S A (2004)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1073/pnas.0401626101"}], "href": "https://doi.org/10.1073/pnas.0401626101"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "15069197"}], "href": "https://pubmed.ncbi.nlm.nih.gov/15069197"}]}, {"type": "r", "ref": 17, "children": [{"type": "t", "text": "Yukiko Asaka, Denis G M Jugloff, Liang Zhang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Hippocampal synaptic plasticity is impaired in the Mecp2-null mouse model of Rett syndrome."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Neurobiol Dis (2006)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.nbd.2005.07.005"}], "href": "https://doi.org/10.1016/j.nbd.2005.07.005"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "16087343"}], "href": "https://pubmed.ncbi.nlm.nih.gov/16087343"}]}, {"type": "r", "ref": 18, "children": [{"type": "t", "text": "Paolo Moretti, J Adriaan Bouwknecht, Ryan Teague, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Hum Mol Genet (2005)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/hmg/ddi016"}], "href": "https://doi.org/10.1093/hmg/ddi016"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "15548546"}], "href": "https://pubmed.ncbi.nlm.nih.gov/15548546"}]}, {"type": "r", "ref": 19, "children": [{"type": "t", "text": "Sonia Cohen, Harrison W Gabel, Martin Hemberg, et al. 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"}, {"type": "b", "children": [{"type": "t", "text": "Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Neurosci (2005)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1523/JNEUROSCI.4373-05.2005"}], "href": "https://doi.org/10.1523/JNEUROSCI.4373-05.2005"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "16354910"}], "href": "https://pubmed.ncbi.nlm.nih.gov/16354910"}]}, {"type": "r", "ref": 21, "children": [{"type": "t", "text": "Izumi Maezawa, Susan Swanberg, Danielle Harvey, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Neurosci (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1523/JNEUROSCI.0324-09.2009"}], "href": "https://doi.org/10.1523/JNEUROSCI.0324-09.2009"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19386901"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19386901"}]}, {"type": "r", "ref": 22, "children": [{"type": "t", "text": "Lin Chen, Kaifu Chen, Laura A Lavery, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MeCP2 binds to non-CG methylated DNA as neurons mature, influencing transcription and the timing of onset for Rett syndrome."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Proc Natl Acad Sci U S A (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1073/pnas.1505909112"}], "href": "https://doi.org/10.1073/pnas.1505909112"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25870282"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25870282"}]}, {"type": "r", "ref": 23, "children": [{"type": "t", "text": "Jacque P K Ip, Nikolaos Mellios, Mriganka Sur "}, {"type": "b", "children": [{"type": "t", "text": "Rett syndrome: insights into genetic, molecular and circuit mechanisms."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Rev Neurosci (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s41583-018-0006-3"}], "href": "https://doi.org/10.1038/s41583-018-0006-3"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "29740174"}], "href": "https://pubmed.ncbi.nlm.nih.gov/29740174"}]}, {"type": "r", "ref": 24, "children": [{"type": "t", "text": "Shay Ben-Shachar, Maria Chahrour, Christina Thaller, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Hum Mol Genet (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/hmg/ddp181"}], "href": "https://doi.org/10.1093/hmg/ddp181"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19369296"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19369296"}]}, {"type": "r", "ref": 25, "children": [{"type": "t", "text": "Mari Kondo, Laura J Gray, Gregory J Pelka, et al. 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| Synonyms | HSA-MIR-8077 |
| NCBI Gene ID | 102465875 |
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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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MIR8077 has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.
Click the + buttons to view associations for MIR8077 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary |
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