4.8 Article

Human-Specific NOTCH2NL Genes Expand Cortical Neurogenesis through Delta/Notch Regulation

期刊

CELL
卷 173, 期 6, 页码 1370-+

出版社

CELL PRESS
DOI: 10.1016/j.cell.2018.03.067

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资金

  1. Belgian FRS/FNRS
  2. European Research Council (ERC Adv Grant GENDEVOCORTEX)
  3. FMRE
  4. Interuniversity Attraction Poles Program (IUAP)
  5. WELBIO Program of the Walloon Region
  6. AXA Research Fund
  7. Foundation ULB
  8. ERA-net Microkin
  9. Vlaams Instituut voor Biotechnologie (VIB)
  10. EMBO Fellowships
  11. L'Oreal-Unesco for Women in Sciences fellowship

向作者/读者索取更多资源

The cerebral cortex underwent rapid expansion and increased complexity during recent hominid evolution. Gene duplications constitute a major evolutionary force, but their impact on human brain development remains unclear. Using tailored RNA sequencing (RNA-seq), we profiled the spatial and temporal expression of hominid-specific duplicated (HS) genes in the human fetal cortex and identified a repertoire of 35 HS genes displaying robust and dynamic patterns during cortical neurogenesis. Among them NOTCH2NL, human-specific paralogs of the NOTCH2 receptor, stood out for their ability to promote cortical progenitor maintenance. NOTCH2NL promote the clonal expansion of human cortical progenitors, ultimately leading to higher neuronal output. At the molecular level, NOTCH2NL function by activating the Notch pathway through inhibition ofcisDelta/Notch interactions. Our study uncovers a large repertoire of recently evolved genes active during human corticogenesis and reveals how human-specific NOTCH paralogs may have contributed to the expansion of the human cortex.

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