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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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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. |
format | Online Article Text |
id | pubmed-10491382 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
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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