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Using rare genetic mutations to revisit structural brain asymmetry.

Authors :
Kopal J
Kumar K
Shafighi K
Saltoun K
Modenato C
Moreau CA
Huguet G
Jean-Louis M
Martin CO
Saci Z
Younis N
Douard E
Jizi K
Beauchamp-Chatel A
Kushan L
Silva AI
van den Bree MBM
Linden DEJ
Owen MJ
Hall J
Lippé S
Draganski B
Sønderby IE
Andreassen OA
Glahn DC
Thompson PM
Bearden CE
Zatorre R
Jacquemont S
Bzdok D
Source :
Nature communications [Nat Commun] 2024 Mar 26; Vol. 15 (1), pp. 2639. Date of Electronic Publication: 2024 Mar 26.
Publication Year :
2024

Abstract

Asymmetry between the left and right hemisphere is a key feature of brain organization. Hemispheric functional specialization underlies some of the most advanced human-defining cognitive operations, such as articulated language, perspective taking, or rapid detection of facial cues. Yet, genetic investigations into brain asymmetry have mostly relied on common variants, which typically exert small effects on brain-related phenotypes. Here, we leverage rare genomic deletions and duplications to study how genetic alterations reverberate in human brain and behavior. We designed a pattern-learning approach to dissect the impact of eight high-effect-size copy number variations (CNVs) on brain asymmetry in a multi-site cohort of 552 CNV carriers and 290 non-carriers. Isolated multivariate brain asymmetry patterns spotlighted regions typically thought to subserve lateralized functions, including language, hearing, as well as visual, face and word recognition. Planum temporale asymmetry emerged as especially susceptible to deletions and duplications of specific gene sets. Targeted analysis of common variants through genome-wide association study (GWAS) consolidated partly diverging genetic influences on the right versus left planum temporale structure. In conclusion, our gene-brain-behavior data fusion highlights the consequences of genetically controlled brain lateralization on uniquely human cognitive capacities.<br /> (© 2024. The Author(s).)

Details

Language :
English
ISSN :
2041-1723
Volume :
15
Issue :
1
Database :
MEDLINE
Journal :
Nature communications
Publication Type :
Academic Journal
Accession number :
38531844
Full Text :
https://doi.org/10.1038/s41467-024-46784-w