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Relationship between sex biases in gene expression and sex biases in autism and Alzheimer’s disease

Sex differences in the brain may play an important role in sex-differential prevalence of neuropsychiatric conditions. In order to understand the transcriptional basis of sex differences, we analyzed multiple, large-scale, human postmortem brain RNA-seq datasets using both within-region and pan-regi...

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Autores principales: Fass, Stuart B., Mulvey, Bernard, Yang, Wei, Selmanovic, Din, Chaturvedi, Sneha, Tycksen, Eric, Weiss, Lauren A., Dougherty, Joseph D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10491382/
https://www.ncbi.nlm.nih.gov/pubmed/37693465
http://dx.doi.org/10.1101/2023.08.29.23294773
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author Fass, Stuart B.
Mulvey, Bernard
Yang, Wei
Selmanovic, Din
Chaturvedi, Sneha
Tycksen, Eric
Weiss, Lauren A.
Dougherty, Joseph D.
author_facet Fass, Stuart B.
Mulvey, Bernard
Yang, Wei
Selmanovic, Din
Chaturvedi, Sneha
Tycksen, Eric
Weiss, Lauren A.
Dougherty, Joseph D.
author_sort Fass, Stuart B.
collection PubMed
description Sex differences in the brain may play an important role in sex-differential prevalence of neuropsychiatric conditions. In order to understand the transcriptional basis of sex differences, we analyzed multiple, large-scale, human postmortem brain RNA-seq datasets using both within-region and pan-regional frameworks. We find evidence of sex-biased transcription in many autosomal genes, some of which provide evidence for pathways and cell population differences between chromosomally male and female individuals. These analyses also highlight regional differences in the extent of sex-differential gene expression. We observe an increase in specific neuronal transcripts in male brains and an increase in immune and glial function-related transcripts in female brains. Integration with single-cell data suggests this corresponds to sex differences in cellular states rather than cell abundance. Integration with case-control gene expression studies suggests a female molecular predisposition towards Alzheimer’s disease, a female-biased disease. Autism, a male-biased diagnosis, does not exhibit a male predisposition pattern in our analysis. Finally, we provide region specific analyses of sex differences in brain gene expression to enable additional studies at the interface of gene expression and diagnostic differences.
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spelling pubmed-104913822023-09-09 Relationship between sex biases in gene expression and sex biases in autism and Alzheimer’s disease Fass, Stuart B. Mulvey, Bernard Yang, Wei Selmanovic, Din Chaturvedi, Sneha Tycksen, Eric Weiss, Lauren A. Dougherty, Joseph D. medRxiv Article Sex differences in the brain may play an important role in sex-differential prevalence of neuropsychiatric conditions. In order to understand the transcriptional basis of sex differences, we analyzed multiple, large-scale, human postmortem brain RNA-seq datasets using both within-region and pan-regional frameworks. We find evidence of sex-biased transcription in many autosomal genes, some of which provide evidence for pathways and cell population differences between chromosomally male and female individuals. These analyses also highlight regional differences in the extent of sex-differential gene expression. We observe an increase in specific neuronal transcripts in male brains and an increase in immune and glial function-related transcripts in female brains. Integration with single-cell data suggests this corresponds to sex differences in cellular states rather than cell abundance. Integration with case-control gene expression studies suggests a female molecular predisposition towards Alzheimer’s disease, a female-biased disease. Autism, a male-biased diagnosis, does not exhibit a male predisposition pattern in our analysis. Finally, we provide region specific analyses of sex differences in brain gene expression to enable additional studies at the interface of gene expression and diagnostic differences. Cold Spring Harbor Laboratory 2023-09-01 /pmc/articles/PMC10491382/ /pubmed/37693465 http://dx.doi.org/10.1101/2023.08.29.23294773 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Fass, Stuart B.
Mulvey, Bernard
Yang, Wei
Selmanovic, Din
Chaturvedi, Sneha
Tycksen, Eric
Weiss, Lauren A.
Dougherty, Joseph D.
Relationship between sex biases in gene expression and sex biases in autism and Alzheimer’s disease
title Relationship between sex biases in gene expression and sex biases in autism and Alzheimer’s disease
title_full Relationship between sex biases in gene expression and sex biases in autism and Alzheimer’s disease
title_fullStr Relationship between sex biases in gene expression and sex biases in autism and Alzheimer’s disease
title_full_unstemmed Relationship between sex biases in gene expression and sex biases in autism and Alzheimer’s disease
title_short Relationship between sex biases in gene expression and sex biases in autism and Alzheimer’s disease
title_sort relationship between sex biases in gene expression and sex biases in autism and alzheimer’s disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10491382/
https://www.ncbi.nlm.nih.gov/pubmed/37693465
http://dx.doi.org/10.1101/2023.08.29.23294773
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