A dyad of human-specific <i>NBPF14</i> and <i>NOTCH2NLB</i> orchestrates cortical progenitor abundance crucial for human neocortex expansion.

Abstract

We determined the roles of two coevolved and coexpressed human-specific genes, <i>NBPF14</i> and <i>NOTCH2NLB</i>, on the abundance of the cortical progenitors that underlie the evolutionary expansion of the neocortex, the seat of higher cognitive abilities in humans. Using automated microinjection into apical progenitors (APs) of embryonic mouse neocortex and electroporation of APs in chimpanzee cerebral organoids, we show that <i>NBPF14</i> promotes the delamination of AP progeny, by promoting oblique cleavage plane orientation during AP division, leading to increased abundance of the key basal progenitor type, basal radial glia. In contrast, <i>NOTCH2NLB</i> promotes AP proliferation, leading to expansion of the AP pool. When expressed together, <i>NBPF14</i> and <i>NOTCH2NLB</i> exert coordinated effects, resulting in expansion of basal progenitors while maintaining self-renewal of APs. Hence, these two human-specific genes orchestrate the behavior of APs, and the lineages of their progeny, in a manner essential for the evolutionary expansion of the human neocortex.