Molecular and cellular evolution of the primate dorsolateral prefrontal cortex.
Shaojie MaMario ŠkaricaQian LiChuan XuRyan D RisgaardAndrew T N TebbenkampXoel Mato BlancoRothem KovnerŽeljka KrsnikXabier de MartinVictor LuriaXavier Martí-PérezDan LiangAmir KargerDanielle K SchmidtZachary Gomez-SanchezCai QiKevin T GobeskeSirisha PochareddyAshwin DebnathCade J HottmanJoshua SpurrierLeon TeoAnthony G BoghdadiJihane Homman-LudiyeJohn J ElyEtienne W DaadiDa MiMarcel M DaadiOscar MarinPatrick R HofMladen-Roko RasinJames A BourneChet C SherwoodGabriel Santpere BaróMatthew J GirgentiStephen M StrittmatterAndré M M SousaNenad SestanPublished in: Science (New York, N.Y.) (2022)
The granular dorsolateral prefrontal cortex (dlPFC) is an evolutionary specialization of primates that is centrally involved in cognition. We assessed more than 600,000 single-nucleus transcriptomes from adult human, chimpanzee, macaque, and marmoset dlPFC. Although most cell subtypes defined transcriptomically are conserved, we detected several that exist only in a subset of species as well as substantial species-specific molecular differences across homologous neuronal, glial, and non-neural subtypes. The latter are exemplified by human-specific switching between expression of the neuropeptide somatostatin and tyrosine hydroxylase, the rate-limiting enzyme in dopamine production in certain interneurons. The above molecular differences are also illustrated by expression of the neuropsychiatric risk gene FOXP2 , which is human-specific in microglia and primate-specific in layer 4 granular neurons. We generated a comprehensive survey of the dlPFC cellular repertoire and its shared and divergent features in anthropoid primates.
Keyphrases
- prefrontal cortex
- endothelial cells
- poor prognosis
- induced pluripotent stem cells
- pluripotent stem cells
- single cell
- spinal cord
- genome wide
- transcription factor
- regulatory t cells
- single molecule
- multiple sclerosis
- neuropathic pain
- oxidative stress
- immune response
- transcranial magnetic stimulation
- binding protein
- mild cognitive impairment
- copy number
- childhood cancer