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Authordc.contributor.authorGallardo, Viviana E. 
Authordc.contributor.authorLiang, Jin es_CL
Authordc.contributor.authorBehra, Martine es_CL
Authordc.contributor.authorElkahloun, Abdel es_CL
Authordc.contributor.authorVillablanca, Eduardo J. es_CL
Authordc.contributor.authorRusso, Vincenzo es_CL
Authordc.contributor.authorAllende Connelly, Miguel es_CL
Authordc.contributor.authorBurgess, Shawn M. es_CL
Admission datedc.date.accessioned2011-05-19T17:23:45Z
Available datedc.date.available2011-05-19T17:23:45Z
Publication datedc.date.issued2010-12-13
Cita de ítemdc.identifier.citationBMC DEVELOPMENTAL BIOLOGY, Volume: 10, Article Number: 120, 2010es_CL
Identifierdc.identifier.issn1471-213X
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/119207
General notedc.descriptionArtículo de publicación ISIes_CL
Abstractdc.description.abstractBackground: Development of the posterior lateral line (PLL) system in zebrafish involves cell migration, proliferation and differentiation of mechanosensory cells. The PLL forms when cranial placodal cells delaminate and become a coherent, migratory primordium that traverses the length of the fish to form this sensory system. As it migrates, the primordium deposits groups of cells called neuromasts, the specialized organs that contain the mechanosensory hair cells. Therefore the primordium provides both a model for studying collective directional cell migration and the differentiation of sensory cells from multipotent progenitor cells. Results: Through the combined use of transgenic fish, Fluorescence Activated Cell Sorting and microarray analysis we identified a repertoire of key genes expressed in the migrating primordium and in differentiated neuromasts. We validated the specific expression in the primordium of a subset of the identified sequences by quantitative RTPCR, and by in situ hybridization. We also show that interfering with the function of two genes, f11r and cd9b, defects in primordium migration are induced. Finally, pathway construction revealed functional relationships among the genes enriched in the migrating cell population. Conclusions: Our results demonstrate that this is a robust approach to globally analyze tissue-specific expression and we predict that many of the genes identified in this study will show critical functions in developmental events involving collective cell migration and possibly in pathological situations such as tumor metastasis.es_CL
Patrocinadordc.description.sponsorshipThis work was supported by grants to M.A. from Fondecyt (1070867), ICM (P06-039F) and FONDAP (15090007). V.G. was supported by a Conicyt fellowship and travel fellowships from the Vicerrectoría de Asuntos Académicos, Departamento de Postgrado y Postítulo, Universidad de Chile and MECESUP. This research was supported by the Intramural Research Program of the National Human Genome Research Institute, National Institutes of Health (S.B.).es_CL
Lenguagedc.language.isoenes_CL
Publisherdc.publisherBIOMED CENTRALes_CL
Keywordsdc.subjectCOLLECTIVE CELL-MIGRATIONes_CL
Títulodc.titleMolecular dissection of the migrating posterior lateral line primordium during early development in zebrafishes_CL
Document typedc.typeArtículo de revista


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