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dc.contributor.authorDonahue, Christine Patricia
dc.contributor.authorNi, Jake
dc.contributor.authorRozners, Eriks
dc.contributor.authorGlicksman, Marcie A.
dc.contributor.authorWolfe, Michael S.
dc.date2022-08-11T08:08:58.000
dc.date.accessioned2022-08-23T16:14:03Z
dc.date.available2022-08-23T16:14:03Z
dc.date.issued2007-05-26
dc.date.submitted2008-09-22
dc.identifier.citationJ Biomol Screen. 2007 Sep;12(6):789-99. Epub 2007 May 24. <a href="http://dx.doi.org/10.1177/1087057107302676">Link to article on publisher's site</a>
dc.identifier.issn1087-0571 (Print)
dc.identifier.doi10.1177/1087057107302676
dc.identifier.pmid17525136
dc.identifier.urihttp://hdl.handle.net/20.500.14038/33771
dc.description.abstractAlternative 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.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=17525136&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1177/1087057107302676
dc.subjectAminoglycosides; 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
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleIdentification of tau stem loop RNA stabilizers
dc.typeJournal Article
dc.source.journaltitleJournal of biomolecular screening : the official journal of the Society for Biomolecular Screening
dc.source.volume12
dc.source.issue6
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/431
dc.identifier.contextkey635306
html.description.abstract<p>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.</p>
dc.identifier.submissionpathgsbs_sp/431
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.source.pages789-99


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