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FGF4 regulates blood and muscle specification in Xenopus laevis.
Isaacs, Harry V; Deconinck, Anne E; Pownall, Mary E.
Afiliación
  • Isaacs HV; Area 11, Department of Biology, University of York, York YO10 5YW, U.K.
Biol Cell ; 99(3): 165-73, 2007 Mar.
Article en En | MEDLINE | ID: mdl-17092209
ABSTRACT
BACKGROUND INFORMATION FGF (fibroblast growth factor) signalling is known to be required for many aspects of mesoderm formation and patterning during Xenopus development and has been implicated in regulating genes required for the specification of both blood and skeletal muscle lineages.

RESULTS:

In the present study, we have specifically knocked down the expression of FGF4 using AMO (antisense morpholino oligonucleotide)-mediated inhibition and demonstrate that FGF4 acts in the dorsal marginal zone to restrict blood development and promote the development of skeletal muscle. In addition, we used a drug inhibitor of FGF signalling and an inducible form of FGFR1 (FGF receptor 1) to identify a period of competence during late blastula and gastrula stages when FGF signalling acts to regulate blood versus muscle specification. Notably, we found that it is the dorsal activity of FGF that is required to restrict the expression of SCL (stem cell leukaemia) to the ventral blood island.

CONCLUSIONS:

Our data indicate that FGF4 is a key organizer-derived signal involved in the process of dorsoventral patterning of the mesoderm.
Asunto(s)
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Xenopus laevis / Células Sanguíneas / Músculo Esquelético / Tipificación del Cuerpo / Factor 4 de Crecimiento de Fibroblastos / Mesodermo Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Biol Cell Año: 2007 Tipo del documento: Article País de afiliación: Reino Unido
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Xenopus laevis / Células Sanguíneas / Músculo Esquelético / Tipificación del Cuerpo / Factor 4 de Crecimiento de Fibroblastos / Mesodermo Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Biol Cell Año: 2007 Tipo del documento: Article País de afiliación: Reino Unido