Atypical genomic cortical patterning in autism with poor early language outcome
Michael Vincent LombardoiD, Lisa T. EyleriD, Tiziano PramparoiD, Vahid GazestaniiD, Donald J. HagleriD, Chi‐Hua CheniD, Anders Martin DaleiD, Jakob SeidlitziD, Richard A. I. BethlehemiD, Natasha BertelseniD, Cynthia Carter BarnesiD, Linda LopeziD, Kathleen M CampbelliD, Nathan E. LewisiD, Karen PierceiD, Eric CourchesneiD
Abstract
Cortical regional identities develop through anterior-posterior (A-P) and dorsal-ventral (D-V) prenatal genomic patterning gradients. Here we find that A-P and D-V genomic patterning of cortical surface area (SA) and thickness (CT) is intact in typically developing and autistic toddlers with good language outcome, but is absent in autistic toddlers with poor early language outcome. Genes driving this effect are prominent in midgestational A-P and D-V gene expression gradients and prenatal cell types driving SA and CT variation (e.g., progenitor cells versus excitatory neurons). These genes are also important for vocal learning, human-specific evolution, and prenatal co-expression networks enriched for high-penetrance autism risk genes. Autism with poor early language outcome may be linked to atypical genomic cortical patterning starting in prenatal periods and which impacts later development of regional functional specialization and circuit formation. One Sentence SummaryGenomic patterning of the cortex is atypical in autistic toddlers with poor early language outcome.
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