| HGNC Family | Non-coding RNAs |
| Name | microRNA 4457 |
| 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 provided abstracts collectively focus on the functions of the transport proteins ENT4/PMAT (encoded by SLC29A4), which regulate the transport of adenosine and monoamine neurotransmitters. For example, one study demonstrated that ENT4 mediates pH‐dependent adenosine transport in ventricular myocytes and endothelial cells, suggesting an important role in heart function—especially under acidic, ischemic conditions."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": " In another investigation, PMAT was shown to be abundant in the choroid plexus, where its localization on the cerebrospinal fluid–facing membrane aligns with its role in removing neuroactive amines and xenobiotic cations from the CSF, thereby protecting the brain."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nAdditional work evaluated the impact of SLC29A4 deletion on vascular function, revealing that the loss of ENT4 influences hemodynamics and vascular reactivity in a sex‐specific manner. In mice lacking ENT4, there were distinct changes in myogenic tone and responses to adenosine and serotonin, underscoring the transporters’ contributions to blood flow regulation."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nFurther studies addressing PMAT’s function found that alterations in its expression modulate behavioral responses to antidepressant and psychostimulant drugs, as well as stress-induced neuroendocrine changes, again with notable sex differences. These data suggest that, under conditions where primary monoamine transporters are compromised, PMAT plays a critical, albeit modulatory, role in monoaminergic signaling."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIt is important to note that while these abstracts provide substantial insight into the roles of ENT4/PMAT in cardiovascular, cerebrospinal, and behavioral functions, none of them mention or address the function of MIR4457. As such, the current body of work does not offer any information on MIR4457, and its role remains to be elucidated in future research.\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Kay Barnes, Halina Dobrzynski, Sophie Foppolo, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Distribution and functional characterization of equilibrative nucleoside transporter-4, a novel cardiac adenosine transporter activated at acidic pH."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Circ Res (2006)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1161/01.RES.0000238359.18495.42"}], "href": "https://doi.org/10.1161/01.RES.0000238359.18495.42"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "16873718"}], "href": "https://pubmed.ncbi.nlm.nih.gov/16873718"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Haichuan Duan, Joanne Wang "}, {"type": "b", "children": [{"type": "t", "text": "Impaired monoamine and organic cation uptake in choroid plexus in mice with targeted disruption of the plasma membrane monoamine transporter (Slc29a4) gene."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M112.436972"}], "href": "https://doi.org/10.1074/jbc.M112.436972"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23255610"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23255610"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Ran Wei, Stephen L Gust, David Tandio, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Deletion of murine slc29a4 modifies vascular responses to adenosine and 5-hydroxytryptamine in a sexually dimorphic manner."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Physiol Rep (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.14814/phy2.14395"}], "href": "https://doi.org/10.14814/phy2.14395"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32170814"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32170814"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Jasmin N Beaver, Brady L Weber, Matthew T Ford, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Uncovering Functional Contributions of PMAT ("}, {"type": "a", "children": [{"type": "t", "text": "i"}], "href": "i"}, {"type": "t", "text": "Slc29a4"}, {"type": "a", "children": [{"type": "t", "text": "/i"}], "href": "/i"}, {"type": "t", "text": ") to Monoamine Clearance Using Pharmacobehavioral Tools."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cells (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3390/cells11121874"}], "href": "https://doi.org/10.3390/cells11121874"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35741002"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35741002"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Brady L Weber, Marissa M Nicodemus, Allianna K Hite, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Heterotypic Stressors Unmask Behavioral Influences of PMAT Deficiency in Mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Int J Mol Sci (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3390/ijms242216494"}], "href": "https://doi.org/10.3390/ijms242216494"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "38003684"}], "href": "https://pubmed.ncbi.nlm.nih.gov/38003684"}]}]}]}
|
| Synonyms | MIR-4457 |
| NCBI Gene ID | 100616235 |
| API | |
| Download Associations | |
| Predicted Functions |
![]() |
| Co-expressed Genes |
![]() |
| Expression in Tissues and Cell Lines |
![]() |
MIR4457 has 244 functional associations with biological entities spanning 3 categories (molecular profile, cell line, cell type or tissue, gene, protein or microRNA) extracted from 7 datasets.
Click the + buttons to view associations for MIR4457 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| CCLE Cell Line Gene CNV Profiles | cell lines with high or low copy number of MIR4457 gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset. | |
| COSMIC Cell Line Gene CNV Profiles | cell lines with high or low copy number of MIR4457 gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset. | |
| ENCODE Histone Modification Site Profiles | histone modification site profiles with high histone modification abundance at MIR4457 gene from the ENCODE Histone Modification Site Profiles dataset. | |
| ENCODE Transcription Factor Binding Site Profiles | transcription factor binding site profiles with transcription factor binding evidence at the promoter of MIR4457 gene from the ENCODE Transcription Factor Binding Site Profiles dataset. | |
| ENCODE Transcription Factor Targets | transcription factors binding the promoter of MIR4457 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset. | |
| Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles | cell lines with high or low copy number of MIR4457 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset. | |
| Roadmap Epigenomics Histone Modification Site Profiles | histone modification site profiles with high histone modification abundance at MIR4457 gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset. | |