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dc.contributor.authorWang, Junning
dc.contributor.authorTse, Sze-Wah
dc.contributor.authorAndreadis, Athena
dc.date2022-08-11T08:07:57.000
dc.date.accessioned2022-08-23T15:37:19Z
dc.date.available2022-08-23T15:37:19Z
dc.date.issued2006-12-06
dc.date.submitted2010-09-30
dc.identifier.citationJ Neurochem. 2007 Jan;100(2):437-45. Epub 2006 Nov 27. <a href="http://dx.doi.org/10.1111/j.1471-4159.2006.04252.x">Link to article on publisher's site</a>
dc.identifier.issn0022-3042 (Linking)
dc.identifier.doi10.1111/j.1471-4159.2006.04252.x
dc.identifier.pmid17144905
dc.identifier.urihttp://hdl.handle.net/20.500.14038/25689
dc.description.abstractTau is a microtubule-associated protein whose transcript undergoes complex regulated splicing in the mammalian nervous system. Exon 6 of the gene is an alternatively spliced cassette whose expression profile differs from that of the other tau regulated exons, implying the involvement of distinct regulatory factors. Previous work had established the existence and use of two additional 3' splice sites within exon 6 and the influence of splicing factors polypyrimidine binding protein (PTB) and U2AF on its splicing. The present work shows that exon 6 isoforms exist in distinct ratios in different compartments of the nervous system and that splicing of exon 6 is governed by multiple branch points, exonic cis elements and additional trans factors. Recent results show that tau exon 6 is specifically suppressed in the brains of people who suffer from myotonic dystrophy type 1. The understanding of how tau exon 6 splicing is regulated may give us insights into the disease.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=17144905&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1111/j.1471-4159.2006.04252.x
dc.subjectAlternative Splicing
dc.subjectAnimals
dc.subjectCOS Cells
dc.subjectCercopithecus aethiops
dc.subjectExons
dc.subjectGene Expression
dc.subjectHumans
dc.subject*Molecular Sequence Data
dc.subjectMutagenesis
dc.subjectRNA Splice Sites
dc.subjectRNA, Messenger
dc.subjectReverse Transcriptase Polymerase Chain Reaction
dc.subjectTrans-Activators
dc.subjecttau Proteins
dc.subjectCell Biology
dc.titleTau exon 6 is regulated by an intricate interplay of trans factors and cis elements, including multiple branch points
dc.typeJournal Article
dc.source.journaltitleJournal of neurochemistry
dc.source.volume100
dc.source.issue2
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/andreadis/4
dc.identifier.contextkey1587261
html.description.abstract<p>Tau is a microtubule-associated protein whose transcript undergoes complex regulated splicing in the mammalian nervous system. Exon 6 of the gene is an alternatively spliced cassette whose expression profile differs from that of the other tau regulated exons, implying the involvement of distinct regulatory factors. Previous work had established the existence and use of two additional 3' splice sites within exon 6 and the influence of splicing factors polypyrimidine binding protein (PTB) and U2AF on its splicing. The present work shows that exon 6 isoforms exist in distinct ratios in different compartments of the nervous system and that splicing of exon 6 is governed by multiple branch points, exonic cis elements and additional trans factors. Recent results show that tau exon 6 is specifically suppressed in the brains of people who suffer from myotonic dystrophy type 1. The understanding of how tau exon 6 splicing is regulated may give us insights into the disease.</p>
dc.identifier.submissionpathandreadis/4
dc.contributor.departmentShriver Center
dc.contributor.departmentDepartment of Cell Biology
dc.source.pages437-45


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