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First published online March 7, 2005
doi: 10.1242/10.1242/dev.01726


1 Department of Anatomy, University of Cambridge, Downing Street, Cambridge CB2
3DY, UK
2 State Key Laboratory of Brain and Cognitive Science, Institute of Biophysics,
Chinese Academy of Sciences, 15 Datun Road, Beijing 100101, PR China
3 Retinoid Research, Departments of Chemistry and Biology, Allergan, Irvine, CA
92623, USA
4 Dipartimento di Fisiologia e Biochimica, Universita' degli Studi di Pisa, Via
Carducci 13, 56010 Ghezzano (Pisa), Italy
5 AMBISEN Center, High Technology Center for the Study of Environmental Damage
to the Endocrine and Nervous System, Universita' degli Studi di Pisa, Pisa,
Italy
Authors for correspondence (e-mail:
liuy{at}moon.ibp.ac.cn
and
harris{at}mole.bio.cam.ac.uk).
Accepted 18 January 2005
In the developing spinal cord and telencephalon, ventral patterning involves the interplay of Hedgehog (Hh), Retinoic Acid (RA) and Fibroblast Growth Factor (FGF) signaling. In the eye, ventral specification involves Hh signaling, but the roles of RA and FGF signaling are less clear. By overexpression assays in Xenopus embryos, we found that both RA and FGF receptor (FGFR) signaling ventralize the eye, by expanding optic stalk and ventral retina, and repressing dorsal retina character. Co-overexpression experiments show that RA and FGFR can collaborate with Hh signaling and reinforce its ventralizing activity. In loss-of-function experiments, a strong eye dorsalization was observed after triple inhibition of Hh, RA and FGFR signaling, while weaker effects were obtained by inhibiting only one or two of these pathways. These results suggest that the ventral regionalization of the eye is specified by interactions of Hh, RA and FGFR signaling. We argue that similar mechanisms might control ventral neural patterning throughout the central nervous system.
Key words: Ventral retina, Dorsal retina, Optic stalk, Retinoic acid, Hedgehog, FGF receptor, Xenopus
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