| Literature DB >> 25583500 |
François Leroy1, Qing Cai2, Stephanie L Bogart3, Jessica Dubois4, Olivier Coulon5, Karla Monzalvo4, Clara Fischer6, Hervé Glasel4, Lise Van der Haegen7, Audrey Bénézit4, Ching-Po Lin8, David N Kennedy9, Aya S Ihara10, Lucie Hertz-Pannier11, Marie-Laure Moutard12, Cyril Poupon13, Marc Brysbaert6, Neil Roberts14, William D Hopkins3, Jean-François Mangin6, Ghislaine Dehaene-Lambertz4.
Abstract
Identifying potentially unique features of the human cerebral cortex is a first step to understanding how evolution has shaped the brain in our species. By analyzing MR images obtained from 177 humans and 73 chimpanzees, we observed a human-specific asymmetry in the superior temporal sulcus at the heart of the communication regions and which we have named the "superior temporal asymmetrical pit" (STAP). This 45-mm-long segment ventral to Heschl's gyrus is deeper in the right hemisphere than in the left in 95% of typical human subjects, from infanthood till adulthood, and is present, irrespective of handedness, language lateralization, and sex although it is greater in males than in females. The STAP also is seen in several groups of atypical subjects including persons with situs inversus, autistic spectrum disorder, Turner syndrome, and corpus callosum agenesis. It is explained in part by the larger number of sulcal interruptions in the left than in the right hemisphere. Its early presence in the infants of this study as well as in fetuses and premature infants suggests a strong genetic influence. Because this asymmetry is barely visible in chimpanzees, we recommend the STAP region during midgestation as an important phenotype to investigate asymmetrical variations of gene expression among the primate lineage. This genetic target may provide important insights regarding the evolution of the crucial cognitive abilities sustained by this sulcus in our species, namely communication and social cognition.Entities:
Keywords: STS; anatomy; asymmetry; brain; human-specific
Mesh:
Year: 2015 PMID: 25583500 PMCID: PMC4313811 DOI: 10.1073/pnas.1412389112
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205