FGF4 regulates blood and muscle specification in Xenopus laevis.

Biol Cell

Area 11, Department of Biology, University of York, York YO10 5YW, U.K.

Published: March 2007

AI Article Synopsis

  • FGF signalling is crucial for mesoderm development and influences blood and skeletal muscle lineage specification in Xenopus.
  • In the study, knockdown of FGF4 revealed its role in limiting blood development while promoting skeletal muscle formation in specific regions during early developmental stages.
  • The findings highlight FGF4 as a significant signal in dorsoventral patterning of the mesoderm, particularly affecting the expression of SCL in relation to blood development.

Article 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.

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Source
http://dx.doi.org/10.1042/BC20060103DOI Listing

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