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dc.contributor.authorNavas, Luis F. de-
dc.contributor.authorReed, Hilary-
dc.contributor.authorAkam, Michael-
dc.contributor.authorBarrio, Rosa-
dc.contributor.authorAlonso, Claudio R.-
dc.contributor.authorSánchez-Herrero, Ernesto-
dc.date.accessioned2011-03-29T14:06:17Z-
dc.date.available2011-03-29T14:06:17Z-
dc.date.issued2011-01-
dc.identifier.citationDevelopment - Cambridge 138(1):107-16 (2011)es_ES
dc.identifier.issn0950-1991-
dc.identifier.urihttp://hdl.handle.net/10261/33885-
dc.descriptionSupplementary material for this article is available at http://dev.biologists.org/lookup/suppl/doi:10.1242/dev.051409/-/DC1es_ES
dc.description.abstractAlthough most metazoan genes undergo alternative splicing, the functional relevance of the majority of alternative splicing products is still unknown. Here we explore this problem in the Drosophila Hox gene Ultrabithorax (Ubx). Ubx produces a family of six protein isoforms through alternative splicing. To investigate the functional specificity of the Ubx isoforms, we studied their role during the formation of the Drosophila halteres, small dorsal appendages that are essential for normal flight. Our work shows that isoform Ia, which is encoded by all Ubx exons, is more efficient than isoform IVa, which lacks the amino acids coded by two small exons, in controlling haltere development and regulating Ubx downstream targets. However, our experiments also demonstrate that the functional differences among the Ubx isoforms can be compensated for by increasing the expression levels of the less efficient form. The analysis of the DNA-binding profiles of Ubx isoforms to a natural Ubx target, spalt, shows no major differences in isoform DNA-binding activities, suggesting that alternative splicing might primarily affect the regulatory capacity of the isoforms rather than their DNA-binding patterns. Our results suggest that to obtain distinct functional outputs during normal development genes must integrate the generation of qualitative differences by alternative splicing to quantitative processes affecting isoform protein expression levels.es_ES
dc.description.sponsorshipThis work has been supported by a New Investigator Grant from the UK's BBSRC to C.R.A. (Refs: BB/E01173X/1, BB/E01173X/2), grants from the Ministerio de Ciencia y Tecnología (no. BFU2005-04342, BFU2008-00632 to E.S. and BFU2008-01884 to R.B., and Consolider CSD2007-00008 to E.S. and R.B.), and an Institutional Grant from the Fundación Ramón Areces. L. de N. was supported by a fellowship from the Spanish Ministerio de Educación y Ciencia. R. B. acknowledges the Government of the Autonomous Community of the Basque Country (PI2009-16 and Etortek Research Programs 2008/2009) and the Bizkaia County.es_ES
dc.language.isoenges_ES
dc.publisherCompany of Biologistses_ES
dc.rightsclosedAccesses_ES
dc.subjectDrosophilaes_ES
dc.subjectUltrabithoraxes_ES
dc.subjectHoxes_ES
dc.subjectAlternative splicinges_ES
dc.subjectSpaltes_ES
dc.titleIntegration of RNA processing and expression level control modulates the function of the Drosophila Hox gene Ultrabithorax during adult development.es_ES
dc.typeartículoes_ES
dc.identifier.doi10.1242/dev.051409-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttp://dx.doi.org/10.1242/dev.051409es_ES
dc.contributor.funderBiotechnology and Biological Sciences Research Council (UK)-
dc.contributor.funderMinisterio de Ciencia y Tecnología (España)-
dc.contributor.funderFundación Ramón Areces-
dc.contributor.funderMinisterio de Educación y Ciencia (España)-
dc.contributor.funderEusko Jaurlaritza-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100000268es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100006280es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/100008054es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003086es_ES
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