A kinase-independent function of cyclin-dependent kinase 6 promotes outer radial glia expansion and neocortical folding

Proc Natl Acad Sci U S A. 2022 Sep 20;119(38):e2206147119. doi: 10.1073/pnas.2206147119. Epub 2022 Sep 12.

Abstract

The neocortex, the center for higher brain function, first emerged in mammals and has become massively expanded and folded in humans, constituting almost half the volume of the human brain. Primary microcephaly, a developmental disorder in which the brain is smaller than normal at birth, results mainly from there being fewer neurons in the neocortex because of defects in neural progenitor cells (NPCs). Outer radial glia (oRGs), NPCs that are abundant in gyrencephalic species but rare in lissencephalic species, are thought to play key roles in the expansion and folding of the neocortex. However, how oRGs expand, whether they are necessary for neocortical folding, and whether defects in oRGs cause microcephaly remain important questions in the study of brain development, evolution, and disease. Here, we show that oRG expansion in mice, ferrets, and human cerebral organoids requires cyclin-dependent kinase 6 (CDK6), the mutation of which causes primary microcephaly via an unknown mechanism. In a mouse model in which increased Hedgehog signaling expands oRGs and intermediate progenitor cells and induces neocortical folding, CDK6 loss selectively decreased oRGs and abolished neocortical folding. Remarkably, this function of CDK6 in oRG expansion did not require its kinase activity, was not shared by the highly similar CDK4 and CDK2, and was disrupted by the mutation causing microcephaly. Therefore, our results indicate that CDK6 is conserved to promote oRG expansion, that oRGs are necessary for neocortical folding, and that defects in oRG expansion may cause primary microcephaly.

Keywords: corticogenesis; cyclin-dependent kinase 6; microcephaly; neocortex; neural progenitor.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cyclin-Dependent Kinase 6* / genetics
  • Cyclin-Dependent Kinase 6* / metabolism
  • Ependymoglial Cells* / cytology
  • Ependymoglial Cells* / enzymology
  • Ferrets
  • Hedgehog Proteins / metabolism
  • Humans
  • Mice
  • Microcephaly* / genetics
  • Neocortex* / abnormalities
  • Neocortex* / enzymology
  • Neural Stem Cells / cytology
  • Neural Stem Cells / enzymology
  • Organoids / embryology

Substances

  • Hedgehog Proteins
  • Cyclin-Dependent Kinase 6