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.
Authors
- John Hover
- Jesse A Gillis (ORCID: https://orcid.org/0000-0002-0936-9774)
- Jonathan M. Werner (ORCID: https://orcid.org/0000-0001-9248-6420)
Institutions
- University of Toronto (CA)
- Cold Spring Harbor Laboratory (US)
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
Funders
- National Institutes of Health
- National Institute of Mental Health