MIR8061 Gene

HGNC Family Non-coding RNAs
Name microRNA 8061
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 MIR8061, the studies collectively underscore the critical regulation of muscle-specific gene expression and function during development and disease. For example, the investigation of the fast skeletal myosin light chain (encoded by Mylpf) in skeletal muscle revealed its absolute necessity for proper skeletal muscle formation during embryogenesis, where interference with its mRNA processing led to dramatic developmental failures and perinatal lethality."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": " Similarly, analyses in a Down syndrome model demonstrated that alterations in key cardiac muscle proteins, such as mlc2a and PEBP, correlate with congenital heart disease phenotypes, emphasizing the importance of finely tuned gene expression in cardiac as well as skeletal muscle contexts."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn parallel, forced expression of the Six1 transcription factor in muscle cells markedly increased the expression of fast-twitch muscle genes—including Mylpf—while also modulating cell cycle progression. This finding points to a regulatory network that not only drives the specification of fast muscle fiber type but also controls muscle cell proliferation."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": " Within such networks, post‐transcriptional modulators like microRNAs are well positioned to fine‐tune gene expression, suggesting that MIR8061, if involved, might be responsible for modulating the levels or timing of such critical transcripts.\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nFurthermore, differential expression of fast skeletal muscle proteins in a murine asthma model underscores wider implications, where overexpression of proteins such as skMLC in airway smooth muscle is linked to structural and functional changes. This observation supports the idea that a microRNA—potentially MIR8061—could act as a post‐transcriptional regulator, integrating signals that impact muscle gene expression across diverse physiological and pathological settings."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Yingcai Wang, Danuta Szczesna-Cordary, Roger Craig, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Fast skeletal muscle regulatory light chain is required for fast and slow skeletal muscle development."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "FASEB J (2007)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1096/fj.06-7538com"}], "href": "https://doi.org/10.1096/fj.06-7538com"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17356007"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17356007"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Yasuhiro Kazuki, Motoshi Kimura, Ryuichi Nishigaki, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Human chromosome 21q22.2-qter carries a gene(s) responsible for downregulation of mlc2a and PEBP in Down syndrome model mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochem Biophys Res Commun (2004)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.bbrc.2004.03.069"}], "href": "https://doi.org/10.1016/j.bbrc.2004.03.069"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "15063784"}], "href": "https://pubmed.ncbi.nlm.nih.gov/15063784"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Wangjun Wu, Zhuqing Ren, Lin Zhang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Overexpression of Six1 gene suppresses proliferation and enhances expression of fast-type muscle genes in C2C12 myoblasts."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell Biochem (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s11010-013-1653-3"}], "href": "https://doi.org/10.1007/s11010-013-1653-3"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23613228"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23613228"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Ho-Young Kim, Taiyoun Rhim, Mi-Hyun Ahn, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The fast skeletal muscle myosin light chain is differentially expressed in smooth muscle cells of OVA-challenged mouse trachea."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cells (2008)"}]}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18319617"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18319617"}]}]}]}
Synonyms HSA-MIR-8061
NCBI Gene ID 102466251
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Predicted Functions View MIR8061's ARCHS4 Predicted Functions.
Co-expressed Genes View MIR8061's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MIR8061's ARCHS4 Predicted Functions.

Functional Associations

MIR8061 has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.

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Dataset Summary