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C3G regulates the size of the cerebral cortex neural precursor population
Author(s) -
Voss Anne K,
Krebs Danielle L,
Thomas Tim
Publication year - 2006
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1038/sj.emboj.7601234
Subject(s) - biology , guanine nucleotide exchange factor , neuroepithelial cell , microbiology and biotechnology , population , cerebral cortex , cytosol , neural stem cell , signal transduction , neuroscience , biochemistry , enzyme , stem cell , demography , sociology
The mechanisms regulating the size of the cerebral cortex are poorly understood. Here, we demonstrate that the Rap1 guanine nucleotide exchange factor, C3G (Grf2, Rapgef1), controls the size of the cerebral precursor population. Mice lacking C3G show overproliferation of the cortical neuroepithelium. C3G‐deficient neuroepithelial cells accumulate nuclear β‐catenin and fail to exit the cell cycle in vivo . C3G mutant neural precursor cells fail to activate Rap1, exhibit activation of Akt/PKB, inhibition of the β‐catenin‐degrading enzyme, Gsk3β and accumulation of cytosolic and nuclear β‐catenin when exposed to growth factors, in vitro . Our results show that the size of the cortical neural precursor population is controlled by C3G‐mediated inhibition of the Ras signalling pathway.

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