Comparative transcriptomics reveals human-specific cortical features

The cognitive abilities of humans are distinctive among primates, but their molecular and cellular substrates are poorly understood. We used comparative single-nucleus transcriptomics to analyze samples of the middle temporal gyrus (MTG) from adult humans, chimpanzees, gorillas, rhesus macaques, and...

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Published inScience (American Association for the Advancement of Science) Vol. 382; no. 6667; p. eade9516
Main Authors Jorstad, Nikolas L., Song, Janet H. T., Exposito-Alonso, David, Suresh, Hamsini, Castro-Pacheco, Nathan, Krienen, Fenna M., Yanny, Anna Marie, Close, Jennie, Gelfand, Emily, Long, Brian, Seeman, Stephanie C., Travaglini, Kyle J., Basu, Soumyadeep, Beaudin, Marc, Bertagnolli, Darren, Crow, Megan, Ding, Song-Lin, Eggermont, Jeroen, Glandon, Alexandra, Goldy, Jeff, Kiick, Katelyn, Kroes, Thomas, McMillen, Delissa, Pham, Trangthanh, Rimorin, Christine, Siletti, Kimberly, Somasundaram, Saroja, Tieu, Michael, Torkelson, Amy, Feng, Guoping, Hopkins, William D., Höllt, Thomas, Keene, C. Dirk, Linnarsson, Sten, McCarroll, Steven A., Lelieveldt, Boudewijn P., Sherwood, Chet C., Smith, Kimberly, Walsh, Christopher A., Dobin, Alexander, Gillis, Jesse, Lein, Ed S., Hodge, Rebecca D., Bakken, Trygve E.
Format Journal Article
LanguageEnglish
Published United States The American Association for the Advancement of Science 13.10.2023
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Summary:The cognitive abilities of humans are distinctive among primates, but their molecular and cellular substrates are poorly understood. We used comparative single-nucleus transcriptomics to analyze samples of the middle temporal gyrus (MTG) from adult humans, chimpanzees, gorillas, rhesus macaques, and common marmosets to understand human-specific features of the neocortex. Human, chimpanzee, and gorilla MTG showed highly similar cell-type composition and laminar organization as well as a large shift in proportions of deep-layer intratelencephalic-projecting neurons compared with macaque and marmoset MTG. Microglia, astrocytes, and oligodendrocytes had more-divergent expression across species compared with neurons or oligodendrocyte precursor cells, and neuronal expression diverged more rapidly on the human lineage. Only a few hundred genes showed human-specific patterning, suggesting that relatively few cellular and molecular changes distinctively define adult human cortical structure.
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These authors contributed equally to this work.
Data analysis: AD, BL, BPL, CAW, DE, EG, ESL, FMK, HS, JC, JE, JG, JG, JHS, KJT, KS, MB, MC, NC, NLJ, SB, SCS, TEB, TH
Writing manuscript: CAW, CCS, DE, ESL, JC, JG, JHS, NLJ, RDH, TEB
Data interpretation: AD, CAW, CCS, DE, ESL, FMK, HS, JC, JG, JG, JHS, KJT, MB, MC, NC, NLJ, RDH, SCS, SD, TEB
Spatial transcriptomic data generation: BL, DM, EG, JC, SCS
Data archive / Infrastructure: JG, SS
Cytosplore Viewer software: BPL, JE, SB, TH, TK
Author contributions
Sample preparation and RNA data generation: AG, AMY, AT, CCS, CDK, CR, DB, DM, ESL, FMK, GF, JG, KS, KS, KW, MT, RDH, SAM, SD, SL, TEB, TP, WDH
ISSN:0036-8075
1095-9203
1095-9203
DOI:10.1126/science.ade9516