Welcome to the new version of CaltechAUTHORS. Login is currently restricted to library staff. If you notice any issues, please email coda@library.caltech.edu
Published June 2005 | public
Journal Article

Sox10 Overexpression Induces Neural Crest-Like Cells From All Dorsoventral Levels of the Neural Tube but Inhibits Differentiation

Abstract

SoxE genes (Sox8, Sox9, and Sox10) are early response genes to neural crest induction. Although the early role of Sox9 has been examined in chick and frog, later roles in neural crest migration and differentiation remain largely unexplored. We first examined which SoxE genes were expressed in trunk neural crest cells and then investigated their function using in ovo electroporation. The results of this analysis reveal that Sox10 is present in migrating neural crest cells, whereas other SoxE genes are only expressed transiently after induction. Ectopic expression of Sox10 in the neural tube at trunk level induced expression of HNK-1 in neuroepithelial cells followed by extensive emigration from all levels of the dorsoventral neuraxis, including the floor plate. Sox10-expressing cells failed to express neuronal, Schwann, or melanocyte markers up to 6 days posttransfection (E8), suggesting these cells were maintained in an undifferentiated state. Overexpression of Sox8 or Sox9 had similar but not identical effects on neuroepithelial cells. These results show that high levels of Sox10, Sox9, or Sox8 expression in the neural tube are capable of inducing a migratory neural crest-like phenotype even in the absence of dorsal signals and can maintain these cells in an undifferentiated state.

Additional Information

© 2005 Wiley-Liss, Inc. Received 16 August 2004; Revised 17 November 2004; Accepted 6 December 2004. Article first published online: 14 Mar 2005. We thank Yoshio Wakamatsu for the MEBL-1 antibody; Yi-Chuan Cheng for chick Sox8, Sox9, and Sox10 cDNA; Mirella Dottori for FoxD3 constructs; Craig Smith for SoxE antibody, Sox8 and Sox9 in situ probes; Masatoshi Takeichi for cadherin-7 antibody; Paul Sharpe for chick Sox9 cDNA; Angela Nieto for the Slug probe; and Cathy Krull for the pMES construct. We also thank the Developmental Studies Hybridoma Bank, developed under the auspices of the NIHCD and maintained by the University of Iowa, Department of Biological Sciences (Iowa City, IA), for the following antibodies: MF20, developed by D.A. Fischmann; 1E8 (P_o), developed by E. Frank; 4C7 (HNF3β), developed by T. Jessell and S. Brenner-Morton; and 56-4H7 (RhoB) developed by T. Jessell. S.J.M. is supported by an Australian Postgraduate Award. V.M.L. is supported by an American Heart Association Postdoctoral Fellowship.

Additional details

Created:
August 22, 2023
Modified:
October 17, 2023