
A new analysis of individual brain cells across several human brain regions reveals subtle but widespread differences in gene activity between male and female brains. This may help explain why some psychiatric and neurological disorders appear to affect the biological sexes differently, researchers report. Males and females, as defined by individuals with an XY and XX chromosomes, respectively, show marked differences in risk, prevalence, and progression of many psychiatric and neurological disorders. While these disparities likely arise from the interplay of biological and social influences, their consistency across cultures and predictable timing over development suggest that sex-determined differences in gene transcription in the brain may play an important role.
To investigate this possibility, researchers at the National Institute of Mental Health conducted a high-resolution analysis of gene expression in the human brain using single-nucleus RNA sequencing (snRNA-seq) on tissue samples from 30 adult individuals (15 male and 15 female). They specifically focused on six cortical regions – some known to exhibit sex differences in brain structure and others not known to – allowing the authors to more precisely compare between molecular and anatomical variation.
The researchers found that biological sex explained only a very small fraction of variation in gene expression across the brain. Nevertheless, the analysis revealed more than 3,000 genes that exhibited some degree of sex-biased transcription in at least one cortical region, and 133 with consistent effects across brain regions and cell types.
While the strongest differences were found in genes located on the sex chromosomes, most sex-related variation occurred in autosomal genes not linked to sex chromosomes and driven predominantly by sex steroid hormones. Notably, many of these genes showing sex-biased expression overlap with genetic variants associated with neuropsychiatric and neurodegenerative disorders, including ADHD, schizophrenia, depression, and Alzheimer’s disease.
“[DeCasien et al.] explicitly acknowledge that sex-related differences reported in their study may originate from differences in socialization and experience,” write Jessica Tollkuhn and Marc Breedlove in a related Perspective.”
“A role for such social influences could be ruled out if sex differences in gene expression are present before birth, and future studies could address this question.”
A new analysis of individual brain cells across several human brain regions reveals subtle but widespread differences in gene activity between male and female brains. This may help explain why some psychiatric and neurological disorders appear to affect the biological sexes differently, researchers report. Males and females, as defined by individuals with an XY and XX chromosomes, respectively, show marked differences in risk, prevalence, and progression of many psychiatric and neurological disorders. While these disparities likely arise from the interplay of biological and social influences, their consistency across cultures and predictable timing over development suggest that sex-determined differences in gene transcription in the brain may play an important role.
To investigate this possibility, researchers at the National Institute of Mental Health conducted a high-resolution analysis of gene expression in the human brain using single-nucleus RNA sequencing (snRNA-seq) on tissue samples from 30 adult individuals (15 male and 15 female). They specifically focused on six cortical regions – some known to exhibit sex differences in brain structure and others not known to – allowing the authors to more precisely compare between molecular and anatomical variation.
The researchers found that biological sex explained only a very small fraction of variation in gene expression across the brain. Nevertheless, the analysis revealed more than 3,000 genes that exhibited some degree of sex-biased transcription in at least one cortical region, and 133 with consistent effects across brain regions and cell types.
While the strongest differences were found in genes located on the sex chromosomes, most sex-related variation occurred in autosomal genes not linked to sex chromosomes and driven predominantly by sex steroid hormones. Notably, many of these genes showing sex-biased expression overlap with genetic variants associated with neuropsychiatric and neurodegenerative disorders, including ADHD, schizophrenia, depression, and Alzheimer’s disease.
“[DeCasien et al.] explicitly acknowledge that sex-related differences reported in their study may originate from differences in socialization and experience,” write Jessica Tollkuhn and Marc Breedlove in a related Perspective.”
“A role for such social influences could be ruled out if sex differences in gene expression are present before birth, and future studies could address this question.”
Citation: DeCasien A R, Auluck P, Liu S, Feng N, Elkahloun A G, Xu Q, Marenco S, Cookson M R, Raznahan A. (2026) Sex effects on gene expression across the human cerebral cortex at cell type resolution. Science 392(6795): eaea9063. [article]
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A new analysis of individual brain cells across several human brain regions reveals subtle but widespread differences in gene activity between male and female brains. This may help explain why some psychiatric and neurological disorders appear to affect the biological sexes differently, researchers report. Males and females, as defined by individuals with an XY and XX chromosomes, respectively, show marked differences in risk, prevalence, and progression of many psychiatric and neurological disorders. While these disparities likely arise from the interplay of biological and social influences, their consistency across cultures and predictable timing over development suggest that sex-determined differences in gene transcription in the brain may play an important role.
To investigate this possibility, researchers at the National Institute of Mental Health conducted a high-resolution analysis of gene expression in the human brain using single-nucleus RNA sequencing (snRNA-seq) on tissue samples from 30 adult individuals (15 male and 15 female). They specifically focused on six cortical regions – some known to exhibit sex differences in brain structure and others not known to – allowing the authors to more precisely compare between molecular and anatomical variation.
The researchers found that biological sex explained only a very small fraction of variation in gene expression across the brain. Nevertheless, the analysis revealed more than 3,000 genes that exhibited some degree of sex-biased transcription in at least one cortical region, and 133 with consistent effects across brain regions and cell types.
While the strongest differences were found in genes located on the sex chromosomes, most sex-related variation occurred in autosomal genes not linked to sex chromosomes and driven predominantly by sex steroid hormones. Notably, many of these genes showing sex-biased expression overlap with genetic variants associated with neuropsychiatric and neurodegenerative disorders, including ADHD, schizophrenia, depression, and Alzheimer’s disease.
“[DeCasien et al.] explicitly acknowledge that sex-related differences reported in their study may originate from differences in socialization and experience,” write Jessica Tollkuhn and Marc Breedlove in a related Perspective.”
“A role for such social influences could be ruled out if sex differences in gene expression are present before birth, and future studies could address this question.”
Citation: DeCasien A R, Auluck P, Liu S, Feng N, Elkahloun A G, Xu Q, Marenco S, Cookson M R, Raznahan A. (2026) Sex effects on gene expression across the human cerebral cortex at cell type resolution. Science 392(6795): eaea9063. [article]
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RNAmel simplifies RNA sequencing data analysis with a reproducible, integrated platform
Heart failure reshapes bone marrow to create inflammation-related immune memory
Overlooked DNA regions surrounding ‘microexons’ hold missing pieces of autism’s genetic puzzle
RiboBA improves detection of hidden protein-coding regions using ribosome profiling
An anti-senescence gene may fight spinal disc deterioration
Scientists identify the neuroblastoma cells that signal poor outcomes
Novel biosensor uses DNA ‘barcodes’ to uncover disease signals in cells
CellART extracts single-cell information from high-resolution spatial transcriptomics
Cell2space restores spatial context to single-cell RNA sequencing data
Urine test may improve bladder cancer diagnosis and guide treatment decisions
DeCoRE – a computational method to resolve RNA structural heterogeneity from RNA structure probing data by direct RNA sequencing
Tracing 700 million years of cell evolution
How should biological replicates be handled in long-read RNA sequencing?
RNA-Seq reveals a new way the developing heart controls its growth
The Human RNome Project Consortium seeks to publish first-ever complete sequence of the body’s RNA
scFlowReport brings multiple single-cell RNA sequencing analyses into one workflow
Long-read RNA sequencing reveals how neurons choose alternative RNA endings
DeOPUS improves cell-type estimates from bulk RNA sequencing
ResolVI improves accuracy in spatial transcriptomics analysis
RNA sequencing reveals transcriptional allele differences in prostate cancer stem cells
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