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FGF signalling controls formation of the apical sensory organ in the cnidarian Nematostella vectensis
Fabian Rentzsch1,*,
Jens H. Fritzenwanker1,
Corinna B. Scholz2, and
Ulrich Technau1,3,*
1 Sars Centre for Marine Molecular Biology, University of Bergen, N-5008 Bergen,
Norway. 2 Miltenyi Biotec, Friedrich-Ebert-Str. 68, 51429 Bergisch-Gladbach,
Germany. 3 Faculty of Life Sciences, University of Vienna, Althanstrasse 14, 1090 Wien,
Austria.
*
Authors for correspondence (e-mails:
ulrich.technau{at}univie.ac.at;
fabian.rentzsch{at}sars.uib.no)
Accepted for publication 12 March 2008.
Abstract:
Fibroblast growth factor (FGF) signalling regulates essentialdevelopmental
processes in vertebrates and invertebrates, butits role during early metazoan
evolution remains obscure. Here,we analyse the function of FGF signalling in
a non-bilateriananimal, the sea anemone Nematostella vectensis. We
identifiedthe complete set of FGF ligands and FGF receptors, of whichtwo
paralogous FGFs (NvFGFa1 and NvFGFa2) and one FGF receptor
(NvFGFRa)are specifically coexpressed in the developing apical
organ,a sensory structure located at the aboral pole of ciliated larvaefrom
various phyla. Morpholino-mediated knockdown experimentsreveal that NvFGFa1
and NvFGFRa are required for the formationof the apical organ, whereas
NvFGFa2 counteracts NvFGFRa signallingto prevent precocious and ectopic
apical organ development.Marker gene expression analysis shows that FGF
signalling regulateslocal patterning in the aboral region. Furthermore,
NvFGFa1activates its own expression and that of the antagonistic
NvFGFa2,thereby establishing positive- and negative-feedback loops.
Finally,we show that loss of the apical organ upon NvFGFa1 knockdown
blocksmetamorphosis into polyps. We propose that the control of the
developmentof sensory structures at the apical pole of ciliated larvaeis an
ancestral function of FGF signalling.
M. Conzelmann, E. A. Williams, S. Tunaru, N. Randel, R. Shahidi, A. Asadulina, J. Berger, S. Offermanns, and G. Jekely (2013)
PNAS
110, 8224-8229
|Abstract »|Full Text »|PDF »
Turing's theory of morphogenesis of 1952 and the subsequent discovery of the crucial role of local self-enhancement and long-range inhibition.
Nematostella vectensis achaete-scute homolog NvashA regulates embryonic ectodermal neurogenesis and represents an ancient component of the metazoan neural specification pathway.
M. J. Layden, M. Boekhout, and M. Q. Martindale (2012)
Development
139, 1013-1022
|Abstract »|Full Text »|PDF »
Nervous systems of the sea anemone Nematostella vectensis are generated by ectoderm and endoderm and shaped by distinct mechanisms.
N. Nakanishi, E. Renfer, U. Technau, and F. Rentzsch (2012)
Development
139, 347-357
|Abstract »|Full Text »|PDF »
Complex functions of Mef2 splice variants in the differentiation of endoderm and of a neuronal cell type in a sea anemone.
A muscle-specific transgenic reporter line of the sea anemone, Nematostella vectensis.
E. Renfer, A. Amon-Hassenzahl, P. R. H. Steinmetz, and U. Technau (2010)
PNAS
107, 104-108
|Abstract »|Full Text »|PDF »
BMPs and Chordin regulate patterning of the directive axis in a sea anemone.
M. Saina, G. Genikhovich, E. Renfer, and U. Technau (2009)
PNAS
106, 18592-18597
|Abstract »|Full Text »|PDF »
The Starlet Sea Anemone Nematostella vectensis: An Anthozoan Model Organism for Studies in Comparative Genomics and Functional Evolutionary Developmental Biology.
G. Genikhovich and U. Technau (2009)
Cold Spring Harb Protoc
2009, pdb.emo129
|Abstract »|Full Text »|PDF »
Anti-acetylated Tubulin Antibody Staining and Phalloidin Staining in the Starlet Sea Anemone Nematostella vectensis.
G. Genikhovich and U. Technau (2009)
Cold Spring Harb Protoc
2009, pdb.prot5283
|Abstract »|Full Text »|PDF »
Evolutionary origins of blastoporal expression and organizer activity of the vertebrate gastrula organizer gene lhx1 and its ancient metazoan paralog lhx3.
Y. Yasuoka, M. Kobayashi, D. Kurokawa, K. Akasaka, H. Saiga, and M. Taira (2009)
Development
136, 2005-2014
|Abstract »|Full Text »|PDF »
FGF ligands in Drosophila have distinct activities required to support cell migration and differentiation.
S. Kadam, A. McMahon, P. Tzou, and A. Stathopoulos (2009)
Development
136, 739-747
|Abstract »|Full Text »|PDF »