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Human-specific gene ARHGAP11B promotes basal progenitor amplification and neocortex expansion

  • Marta Florio
  • , Mareike Albert
  • , Elena Taverna
  • , Takashi Namba
  • , Holger Brandl
  • , Eric Lewitus
  • , Christiane Haffner
  • , Alex Sykes
  • , Fong Kuan Wong
  • , Jula Peters
  • , Elaine Guhr
  • , Sylvia Klemroth
  • , Kay Prüfer
  • , Janet Kelso
  • , Ronald Naumann
  • , Ina Nüsslein
  • , Andreas Dahl
  • , Robert Lachmann
  • , Svante Pääbo
  • , Wieland B. Huttner

研究成果: ジャーナルへの寄稿学術論文査読

抄録

Evolutionary expansion of the human neocortex reflects increased amplification of basal progenitors in the subventricular zone, producing more neurons during fetal corticogenesis. In this work, we analyze the transcriptomes of distinct progenitor subpopulations isolated by a cell polarity-based approach from developing mouse and human neocortex.We identify 56 genes preferentially expressed in human apical and basal radial glia that lack mouse orthologs. Among these, ARHGAP11B has the highest degree of radial glia-specific expression. ARHGAP11B arose from partial duplication of ARHGAP11A (which encodes a Rho guanosine triphosphatase-activating protein) on the human lineage after separation from the chimpanzee lineage. Expression of ARHGAP11B in embryonic mouse neocortex promotes basal progenitor generation and self-renewal and can increase cortical plate area and induce gyrification. Hence, ARHGAP11B may have contributed to evolutionary expansion of human neocortex.

本文言語英語
ページ(範囲)1465-1470
ページ数6
ジャーナルScience
347
6229
DOI
出版ステータス出版済み - 27-03-2015
外部発表はい

All Science Journal Classification (ASJC) codes

  • 一般

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