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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
  • 121
    Citations
  • 0
    Usage
  • 134
    Captures
  • 2
    Mentions
  • 1
    Social Media
Metric Options:   Counts1 Year3 Year

Metrics Details

  • Citations
    121
  • Captures
    134
  • Mentions
    2
    • Blog Mentions
      1
      • 1
    • News Mentions
      1
      • 1
  • Social Media
    1
    • Shares, Likes & Comments
      1
      • Facebook
        1

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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

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

Ju, Xiang-Chun; Hou, Qiong-Qiong; Sheng, Ai-Li; Wu, Kong-Yan; Zhou, Yang; Jin, Ying; Wen, Tieqiao; Yang, Zhengang; Wang, Xiaoqun; Luo, Zhen-Ge

eLife Sciences Organisation, Ltd.

Neuroscience; Biochemistry, Genetics and Molecular Biology; Immunology and Microbiology

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