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First published online June 28, 2004
doi: 10.1242/10.1242/dev.01222
is required for Delta/Notch signalling and cyclic gene expression in the presomitic mesoderm
Developmental Genetics Laboratory, Cancer Research UK, 44 Lincoln's Inn Fields, London WC2A 3PX, UK
Accepted 16 April 2004
Segmentation in vertebrate embryos is controlled by a biochemical
oscillator (`segmentation clock') intrinsic to the cells in the unsegmented
presomitic mesoderm, and is manifested in cyclic transcription of genes
involved in establishing somite polarity and boundaries. We show that the
receptor protein tyrosine phosphatase
(RPTP
) gene
is essential for normal functioning of the somitogenesis clock in
zebrafish. We show that reduction of RPTP
activity using
morpholino antisense oligonucleotides results in severe disruption of the
segmental pattern of the embryo, and loss of cyclic gene expression in the
presomitic mesoderm. Analysis of cyclic genes in RPTP
morphant
embryos indicates an important requirement for RPTP
in the
control of the somitogenesis clock upstream of or in parallel with Delta/Notch
signalling. Impairing RPTP
activity also interferes with convergent
extension during gastrulation. We discuss this dual requirement for
RPTP
in terms of potential functions in Notch and Wnt
signalling.
Key words: Receptor tyrosine phosphatase, Somitogenesis clock, Presomitic mesoderm, Notch signalling, Wnt, Convergent extension, Zebrafish
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