Extended Data Fig. 3: Extended RA-specific GO analysis and spatiotemporal expression of select genes upregulated in the mid-fetal frontal lobe.
From: Regulation of prefrontal patterning and connectivity by retinoic acid

a, Analysis for statistically significant enrichment of upregulated genes during developmental and adult stages for GO terms associated with RA. X-axis represents windows analysed, which are defined at the bottom of the figure. b, Spatiotemporal expression of select genes upregulated in the mid-fetal frontal lobe from Fig. 1 in sixteen neocortical areas across human (red) and macaque (blue) development using BrainSpan (brainspan.org) and PsychENCODE (evolution.psychencode.org) RNA-seq data17,19. Thick full lines represent four PFC areas, thick dotted line represents the primary motor cortex (M1C) and thin dotted lines represent the other non-frontal neocortical areas. Vertical grey box demarcates mid-fetal periods analysed in Fig. 1. Timeline of human and macaque development and the associated periods designed by Kang et al39. shown below. Predicted ages were calculated using the TranscriptomeAge algorithm19, which aligns our earliest macaque samples (PCD 60) with human early mid-fetal samples. Distinct global patterns of spatiotemporal expression were observed. For example, precocious expression in the frontal lobe/PFC followed by broad expression in all eleven neocortical areas (e.g. CBLN2, BDNF), transient enrichment in the frontal lobe/PFC (e.g. WNT11, PCDH17) and downregulation in non-PFC areas during mid-fetal development (e.g. MEIS2).