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Epidermal Growth-Factor – Induced Transcript Isoform Variation Drives Mammary Cell Migration

Signal-induced transcript isoform variation (TIV) includes alternative promoter usage as well as alternative splicing and alternative polyadenylation of mRNA. To assess the phenotypic relevance of signal-induced TIV, we employed exon arrays and breast epithelial cells, which migrate in response to t...

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Detalles Bibliográficos
Autores principales: Köstler, Wolfgang J., Zeisel, Amit, Körner, Cindy, Tsai, Jonathan M., Jacob-Hirsch, Jasmine, Ben-Chetrit, Nir, Sharma, Kirti, Cohen-Dvashi, Hadas, Yitzhaky, Assif, Lader, Eric, Tschulena, Ulrich, Rechavi, Gideon, Domany, Eytan, Wiemann, Stefan, Yarden, Yosef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3855657/
https://www.ncbi.nlm.nih.gov/pubmed/24324612
http://dx.doi.org/10.1371/journal.pone.0080566
Descripción
Sumario:Signal-induced transcript isoform variation (TIV) includes alternative promoter usage as well as alternative splicing and alternative polyadenylation of mRNA. To assess the phenotypic relevance of signal-induced TIV, we employed exon arrays and breast epithelial cells, which migrate in response to the epidermal growth factor (EGF). We show that EGF rapidly – within one hour – induces widespread TIV in a significant fraction of the transcriptome. Importantly, TIV characterizes many genes that display no differential expression upon stimulus. In addition, similar EGF-dependent changes are shared by a panel of mammary cell lines. A functional screen, which utilized isoform-specific siRNA oligonucleotides, indicated that several isoforms play essential, non-redundant roles in EGF-induced mammary cell migration. Taken together, our findings highlight the importance of TIV in the rapid evolvement of a phenotypic response to extracellular signals.