The Primate-Specific Gene TMEM14B Marks Outer Radial Glia Cells and Promotes Cortical Expansion and Folding

Publication date: Available online 12 October 2017
Source:Cell Stem Cell
Author(s): Jing Liu, Wensu Liu, Lu Yang, Qian Wu, Haofeng Zhang, Ai Fang, Long Li, Xiaohui Xu, Le Sun, Jun Zhang, Fuchou Tang, Xiaoqun Wang
Human brain evolution is associated with expansion and folding of the neocortex. Increased diversity in neural progenitor (NP) populations (such as basally located radial glia [RG], which reside in an enlarged outer subventricular zone [OSVZ]) likely contributes to this evolutionary expansion, although their characteristics and relative contributions are only partially understood. Through single-cell transcriptional profiling of sorted human NP subpopulations, we identified the primate-specific TMEM14B gene as a marker of basal RG. Expression of TMEM14B in embryonic NPs induces cortical thickening and gyrification in postnatal mice. This is accompanied by SVZ expansion, the appearance of outer RG-like cells, and the proliferation of multiple NP subsets, with proportional increases in all cortical layers and normal lamination. TMEM14B drives NP proliferation by increasing the phosphorylation and nuclear translocation of IQGAP1, which in turn promotes G1/S cell cycle transitions. These data show that a single primate-specific gene can drive neurodevelopmental changes that contribute to brain evolution.

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Teaser

Wang and colleagues show that the primate-specific gene TMEM14B marks a subset of human neural progenitors and induces cortical folding, providing insights into human brain evolution. Expressing TMEM14B in the fetal mouse brain increases proliferation of progenitor subsets and cortical thickening through nuclear shuttling of IQGAP1, which promotes G1/S transitions.


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