X-linked competition — implications for human development and disease

During early mammalian female development, X chromosome inactivation leads to random transcriptional silencing of one of the two X chromosomes. This inactivation is maintained through subsequent cell divisions, leading to intra-individual diversity, whereby cells express either the maternal or pater...

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Published inNature reviews. Genetics Vol. 26; no. 8; pp. 571 - 580
Main Authors Boone, Philip M., Buenaventura, Teresa, King, James W. D., Merkenschlager, Matthias
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.08.2025
Nature Publishing Group
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ISSN1471-0056
1471-0064
1471-0064
DOI10.1038/s41576-025-00840-3

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Summary:During early mammalian female development, X chromosome inactivation leads to random transcriptional silencing of one of the two X chromosomes. This inactivation is maintained through subsequent cell divisions, leading to intra-individual diversity, whereby cells express either the maternal or paternal X chromosome. Differences in X chromosome sequence content can trigger competitive interactions between clones that may alter organismal development and skew the representation of X-linked sequence variants in a cell-type-specific manner — a recently described phenomenon termed X-linked competition in analogy to existing cell competition paradigms. Skewed representation can define the phenotypic impact of X-linked variants, for example, the manifestation of disease in female carriers of X-linked disease alleles. Here, we review what is currently known about X-linked competition, reflect on what remains to be learnt and map out the implications for X-linked human disease. Differences in X chromosome sequence content can trigger competitive interactions between clones that may alter organismal development and skew the representation of X-linked sequence variants in a cell-type-specific manner. The authors review this recently described phenomenon of X-linked competition and map out the implications for X-linked human diseases.
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ISSN:1471-0056
1471-0064
1471-0064
DOI:10.1038/s41576-025-00840-3