MIR548AY Gene

HGNC Family Non-coding RNAs
Name microRNA 548ay
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 abstracts directly mention MIR548AY, the studies collectively elucidate critical functions for the CRL4 substrate adaptor—commonly referred to as DCAF2, CDT2, or DTL—in ensuring proper cell cycle progression and genomic integrity. Given the shared regulatory networks that govern cell proliferation, DNA replication, and damage repair, it is plausible that MIR548AY—if connected to these pathways—might influence similar cellular processes. For example, in dendritic cells, DCAF2 mediates the polyubiquitination and proteolysis of proteins such as NIK, thereby preventing excessive inflammatory IL-23 production and modulating autoimmune responses."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn early embryogenesis and cell cycle regulation, DCAF2 has emerged as indispensable. Disruption of its function, as demonstrated in murine embryonic models, leads to catastrophic defects such as fragmented mitotic chromosomes, abnormal progression at early cell stages, and ultimately embryonic lethality."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "2", "end_ref": "4"}]}, {"type": "t", "text": " These findings underscore the importance of timely ubiquitin-mediated degradation in maintaining cell cycle fidelity and genome stability.\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nMoreover, the CRL4-DCAF2 complex plays a significant role in safeguarding DNA integrity in the context of cellular stress and disease. In virus-infected cells, for instance, DCAF2 facilitates the degradation of p21—via interactions with PCNA—thus enabling efficient viral replication."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "5"}]}, {"type": "t", "text": " In addition, DCAF2 is critical in T cells where its expression following T cell receptor stimulation ensures proper M phase exit and maintenance of peripheral T cell populations."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "6"}]}, {"type": "t", "text": " Finally, in breast cancer models, DCAF2-dependent ubiquitination of proteins such as RUVBL1 advances non-homologous end-joining repair activity and contributes to radioresistance."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "7"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Tao Huang, Zhengjun Gao, Yu Zhang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "CRL4"}, {"type": "a", "children": [{"type": "t", "text": "sup"}], "href": "sup"}, {"type": "t", "text": "DCAF2"}, {"type": "a", "children": [{"type": "t", "text": "/sup"}], "href": "/sup"}, {"type": "t", "text": " negatively regulates IL-23 production in dendritic cells and limits the development of psoriasis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Exp Med (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1084/jem.20180210"}], "href": "https://doi.org/10.1084/jem.20180210"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30018073"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30018073"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Chao-Lien Liu, I-Shing Yu, Hung-Wei Pan, et al. "}, {"type": "b", "children": [{"type": "t", "text": "L2dtl is essential for cell survival and nuclear division in early mouse embryonic development."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2007)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M606535200"}], "href": "https://doi.org/10.1074/jbc.M606535200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17107960"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17107960"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Yi-Wen Xu, Lan-Rui Cao, Min Wang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Maternal DCAF2 is crucial for maintenance of genome stability during the first cell cycle in mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Sci (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1242/jcs.206664"}], "href": "https://doi.org/10.1242/jcs.206664"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28818995"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28818995"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Man Yang, Mei Liu, Zongting Wang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Mice lacking DCAF2 in placenta die at the gastrulation stage."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Tissue Res (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s00441-022-03655-4"}], "href": "https://doi.org/10.1007/s00441-022-03655-4"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35711069"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35711069"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Richard O Adeyemi, Matthew S Fuller, David J Pintel "}, {"type": "b", "children": [{"type": "t", "text": "Efficient parvovirus replication requires CRL4Cdt2-targeted depletion of p21 to prevent its inhibitory interaction with PCNA."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PLoS Pathog (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1371/journal.ppat.1004055"}], "href": "https://doi.org/10.1371/journal.ppat.1004055"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24699724"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24699724"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Keqi Fan, Fei Wang, Yiyuan Li, et al. "}, {"type": "b", "children": [{"type": "t", "text": "CRL4"}, {"type": "a", "children": [{"type": "t", "text": "sup"}], "href": "sup"}, {"type": "t", "text": "DCAF2"}, {"type": "a", "children": [{"type": "t", "text": "/sup"}], "href": "/sup"}, {"type": "t", "text": " is required for mature T-cell expansion via Aurora B-regulated proteasome activity."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Autoimmun (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.jaut.2018.08.006"}], "href": "https://doi.org/10.1016/j.jaut.2018.08.006"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30245026"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30245026"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Jie Tian, Mingxin Wen, Peng Gao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "RUVBL1 ubiquitination by DTL promotes RUVBL1/2-β-catenin-mediated transcriptional regulation of NHEJ pathway and enhances radiation resistance in breast cancer."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Death Dis (2024)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s41419-024-06651-4"}], "href": "https://doi.org/10.1038/s41419-024-06651-4"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "38609375"}], "href": "https://pubmed.ncbi.nlm.nih.gov/38609375"}]}]}]}
Synonyms HSA-MIR-548AY
NCBI Gene ID 102465247
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Predicted Functions View MIR548AY's ARCHS4 Predicted Functions.
Co-expressed Genes View MIR548AY's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MIR548AY's ARCHS4 Predicted Functions.

Functional Associations

MIR548AY has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.

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Dataset Summary