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    Identification of tau stem loop RNA stabilizers

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    Authors
    Donahue, Christine Patricia
    Ni, Jake
    Rozners, Eriks
    Glicksman, Marcie A.
    Wolfe, Michael S.
    UMass Chan Affiliations
    Graduate School of Biomedical Sciences
    Document Type
    Journal Article
    Publication Date
    2007-05-26
    Keywords
    Aminoglycosides; Base Sequence; Binding, Competitive; Dose-Response Relationship, Drug; Drug Evaluation, Preclinical; Humans; Models, Biological; Nucleic Acid Conformation; Pyrenes; RNA Splicing; RNA Stability; RNA, Messenger; tau Proteins
    Life Sciences
    Medicine and Health Sciences
    
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    Link to Full Text
    http://dx.doi.org/10.1177/1087057107302676
    Abstract
    Alternative splicing of tau exon 10 produces tau isoforms with either 3 (3R) or 4 (4R) repeated microtubule-binding domains. Increased ratios of 4R to 3R tau expression, above the physiological 1:1, leads to neurofibrillary tangles and causes neurodegenerative disease. An RNA stem loop structure plays a significant role in determining the ratio, with decreasing stability correlating with an increase in 4R tau mRNA expression. Recent studies have shown that aminoglycosides are able to bind and stabilize the tau stem loop in vitro, suggesting that other druglike small molecules could be identified and that such molecules might lead to decreased exon 10 splicing in vivo. The authors have developed a fluorescent high-throughput fluorescent binding assay and screened a library of approximately 110,000 compounds to identify candidate drugs that will bind the tau stem loop in vitro. In addition, they have developed a fluorescent-based RNA probe to assay the stabilizing effects of candidate drugs on the tau stem loop RNA. These assays should be applicable to the general problem of identifying small molecules that interact with mRNA secondary structures.
    Source
    J Biomol Screen. 2007 Sep;12(6):789-99. Epub 2007 May 24. Link to article on publisher's site
    DOI
    10.1177/1087057107302676
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/33771
    PubMed ID
    17525136
    Related Resources
    Link to Article in PubMed
    ae974a485f413a2113503eed53cd6c53
    10.1177/1087057107302676
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