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Regulation of neurogenesis by Fgf8a requires Cdc42 signaling and a novel Cdc42 effector protein
Journal article   Open access   Peer reviewed

Regulation of neurogenesis by Fgf8a requires Cdc42 signaling and a novel Cdc42 effector protein

Alissa M Hulstrand and Douglas W Houston
Developmental biology, Vol.382(2), pp.385-399
10/15/2013
DOI: 10.1016/j.ydbio.2013.08.020
PMCID: PMC3846544
PMID: 23994638
url
https://doi.org/10.1016/j.ydbio.2013.08.020View
Published (Version of record) Open Access

Abstract

Fibroblast growth factor (FGF) signaling is required for numerous aspects of neural development, including neural induction, CNS patterning and neurogenesis. The ability of FGFs to activate Ras/MAPK signaling is thought to be critical for these functions. However, it is unlikely that MAPK signaling can fully explain the diversity of responses to FGFs. We have characterized a Cdc42-dependent signaling pathway operating downstream of the Fgf8a splice isoform. We show that a Cdc42 effector 4-like protein (Cdc42ep4-l or Cep4l) has robust neuronal-inducing activity in Xenopus embryos. Furthermore, we find that Cep4l and Cdc42 itself are necessary and sufficient for sensory neurogenesis in vivo. Furthermore, both proteins are involved in Fgf8a-induced neuronal induction, and Cdc42/Cep4l association is promoted specifically by the Fgf8a isoform of Fgf8, but not by Fgf8b, which lacks neuronal inducing activity. Overall, these data suggest a novel role for Cdc42 in an Fgf8a-specific signaling pathway essential for vertebrate neuronal development. •We examine the role of a Cdc42 effector protein (Cep4l) in Xenopus development.•Cep4l binds Cdc42 and induces primary sensory neurogenesis in epidermal regions.•Fgf8a signaling is necessary for and specifically promotes Cdc42/Cep4l binding.•Both Cep4l and Cdc42 are required for Fgf8a-induced primary neurogenesis.
 Xenopus Fgf8 Cdc42 effector protein Neurogenesis Cdc42

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