The hominoid-specific gene TBC1D3 promotes generation of basal neural progenitors and induces cortical folding in mice
eLife, ISSN: 2050-084X, Vol: 5, Issue: AUGUST, Page: e18197
2016
- 121Citations
- 134Captures
- 2Mentions
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- Citations121
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- 121
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- Captures134
- Readers134
- 134
- Mentions2
- Blog Mentions1
- 1
- News Mentions1
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The hominoid-specific gene TBC1D3 promotes generation of basal neural progenitors and induces cortical folding in mice
Research Article ACCEPTED MANUSCRIPT Xiang-Chun Ju Qiong-Qiong Hou Ai-Li Sheng Sheng Kong-Yan Wu Yang Zhou Ying Jin Tieqiao Wen Zhengang Yang Xiaoqun Wang Zhen-Ge Luo
Article Description
Cortical expansion and folding are often linked to the evolution of higher intelligence, but molecular and cellular mechanisms underlying cortical folding remain poorly understood. The hominoid-specific gene TBC1D3 undergoes segmental duplications during hominoid evolution, but its role in brain development has not been explored. Here, we found that expression of TBC1D3 in ventricular cortical progenitors of mice via in utero electroporation caused delamination of ventricular radial glia cells (vRGs) and promoted generation of self-renewing basal progenitors with typical morphology of outer radial glia (oRG), which are most abundant in primates. Furthermore, down-regulation of TBC1D3 in cultured human brain slices decreased generation of oRGs. Interestingly, localized oRG proliferation resulting from either in utero electroporation or transgenic expression of TBC1D3, was often found to underlie cortical regions exhibiting folding. Thus, we have identified a hominoid gene that is required for oRG generation in regulating the cortical expansion and folding.
Bibliographic Details
10.7554/elife.18197; 10.7554/elife.18197.001; 10.7554/elife.18197.017; 10.7554/elife.18197.011; 10.7554/elife.18197.006; 10.7554/elife.18197.002; 10.7554/elife.18197.015; 10.7554/elife.18197.016; 10.7554/elife.18197.028; 10.7554/elife.18197.026; 10.7554/elife.18197.014; 10.7554/elife.18197.003; 10.7554/elife.18197.022; 10.7554/elife.18197.027
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84988484691&origin=inward; http://dx.doi.org/10.7554/elife.18197; http://www.ncbi.nlm.nih.gov/pubmed/27504805; https://elifesciences.org/articles/18197#abstract; http://dx.doi.org/10.7554/elife.18197.001; https://elifesciences.org/articles/18197#fig5; http://dx.doi.org/10.7554/elife.18197.017; https://elifesciences.org/articles/18197#fig3; http://dx.doi.org/10.7554/elife.18197.011; https://elifesciences.org/articles/18197#fig2; http://dx.doi.org/10.7554/elife.18197.006; https://elifesciences.org/articles/18197#digest; http://dx.doi.org/10.7554/elife.18197.002; https://elifesciences.org/articles/18197#media2; http://dx.doi.org/10.7554/elife.18197.015; https://elifesciences.org/articles/18197#fig4; http://dx.doi.org/10.7554/elife.18197.016; http://dx.doi.org/10.7554/elife.18197.028; https://elifesciences.org/articles/18197#fig7; http://dx.doi.org/10.7554/elife.18197.026; https://elifesciences.org/articles/18197#media1; http://dx.doi.org/10.7554/elife.18197.014; https://elifesciences.org/articles/18197#fig1; http://dx.doi.org/10.7554/elife.18197.003; https://elifesciences.org/articles/18197#fig6; http://dx.doi.org/10.7554/elife.18197.022; https://elifesciences.org/articles/18197#author-response; https://elifesciences.org/articles/18197; https://cdn.elifesciences.org/articles/18197/elife-18197-v2.pdf; https://cdn.elifesciences.org/articles/18197/elife-18197-v2.xml; https://elifesciences.org/articles/18197#decision-letter; http://dx.doi.org/10.7554/elife.18197.027; https://dx.doi.org/10.7554/elife.18197
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