The development and evolution of inhibitory neurons in primate cerebrum

Neuroanatomists have long speculated that expanded primate brains contain an increased morphological diversity of inhibitory neurons (INs)(1), and recent studies have identified primate-specific neuronal populations at the molecular level(2). However, we know little about the developmental mechanisms that specify evolutionarily novel cell types in the brain. Here, we reconstructgene expression trajectories specifying INs generated throughout the neurogenic period in macaques and mice by analysing the transcriptomes of 250,181 cells. We find that the initial classes of INs generated prenatally are largely conserved among mammals. Nonetheless, we identify two contrasting developmental mechanisms for specifying evolutionarily novel cell types during prenatal development. First, we show that recently identified primate-specific TAC3 striatal INs are specified by a unique transcriptional programme in progenitors followed by induction of a distinct suite of neuropeptides and neurotransmitter receptors in new-born neurons. Second, we find that multiple classes of transcriptionally conserved olfactory bulb (OB)-bound precursors are redirected to expanded primate white matter and striatum. These classes include a novel peristriatal class of striatum laureatum neuronsthat resemble dopaminergic periglomerular cells ofthe OB. We propose an evolutionary model in which conserved initial classes of neurons supplying the smaller primate OB are reused in the enlarged striatum and cortex. Together, our results provide a unified developmental taxonomy of initial classes of mammalian INs and reveal multiple developmental mechanisms for neural cell type evolution.

Automated summary

This study investigates the gene expression trajectories of inhibitory neurons (INs) in primates and mice during neurogenic period. Researchers find that while the initial classes of INs generated prenatally are largely conserved among mammals, there are contrasting developmental mechanisms for specifying evolutionarily novel cell types during prenatal development.