Population variability in X-chromosome inactivation across 10 mammalian species

One of the two X-chromosomes in female mammals is epigenetically silenced in embryonic stem cells by X-chromosome inactivation. This creates a mosaic of cells expressing either the maternal or the paternal X allele. The X-chromosome inactivation ratio, the proportion of inactivated parental alleles, varies widely among individuals, representing the largest instance of epigenetic variability within mammalian populations. While various contributing factors to X-chromosome inactivation variability are recognized, namely stochastic and/or genetic effects, their relative contributions are poorly understood. This is due in part to limited cross-species analysis, making it difficult to distinguish between generalizable or species-specific mechanisms for X-chromosome inactivation ratio variability. To address this gap, we measure X-chromosome inactivation ratios in ten mammalian species (9531 individual samples), ranging from rodents to primates, and compare the strength of stochastic models or genetic factors for explaining X-chromosome inactivation variability. Our results demonstrate the embryonic stochasticity of X-chromosome inactivation is a general explanatory model for population X-chromosome inactivation variability in mammals, while genetic factors play a minor role.

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Publication Details

Journal
Nature Communications
Published
2024-10-18
DOI
https://doi.org/10.1038/s41467-024-53449-1
Citations
7
Primary Topic
Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Type
article
Field-Weighted Citation Impact
3.85

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article

Population variability in X-chromosome inactivation across 10 mammalian species

John Hover, Jesse A Gillis, Jonathan M. Werner
7 citations
Nature Communications
Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
3.85
article

Population variability in X-chromosome inactivation across 10 mammalian species

John Hover, Jesse A Gillis, Jonathan M. Werner
article en
7 citations

Abstract

One of the two X-chromosomes in female mammals is epigenetically silenced in embryonic stem cells by X-chromosome inactivation. This creates a mosaic of cells expressing either the maternal or the paternal X allele. The X-chromosome inactivation ratio, the proportion of inactivated parental alleles, varies widely among individuals, representing the largest instance of epigenetic variability within mammalian populations. While various contributing factors to X-chromosome inactivation variability are recognized, namely stochastic and/or genetic effects, their relative contributions are poorly understood. This is due in part to limited cross-species analysis, making it difficult to distinguish between generalizable or species-specific mechanisms for X-chromosome inactivation ratio variability. To address this gap, we measure X-chromosome inactivation ratios in ten mammalian species (9531 individual samples), ranging from rodents to primates, and compare the strength of stochastic models or genetic factors for explaining X-chromosome inactivation variability. Our results demonstrate the embryonic stochasticity of X-chromosome inactivation is a general explanatory model for population X-chromosome inactivation variability in mammals, while genetic factors play a minor role.

Nature CommunicationsVol. 15(1)
University of Toronto (CA), Cold Spring Harbor Laboratory (US)
National Institutes of Health, National Institute of Mental Health
Openalex Percentile: Top 6%
Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
3.85
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