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X-chromosome inactivation and its implications for human disease

Joost Gribnau, Tahsin Stefan Barakat
doi: https://doi.org/10.1101/076950
Joost Gribnau
1Department of Developmental Biology, Erasmus MC – University Medical Center, Rotterdam, The Netherlands
Ph.D.
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  • For correspondence: Stefan.Barakat@ed.ac.uk J.Gribnau@erasmusmc.nl
Tahsin Stefan Barakat
2MRC Center for Regenerative Medicine, Institute for Stem Cell Research, School of Biological Sciences, University of Edinburgh, Edinburgh, United Kingdom
M.D., Ph.D.
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  • For correspondence: Stefan.Barakat@ed.ac.uk J.Gribnau@erasmusmc.nl
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ABSTRACT

In humans and other mammals, female cells carry two X-chromosomes, whereas male cells carry a single X and Y-chromosome. To achieve an equal expression level of X-linked genes in both sexes, a dosage compensation mechanism evolved, which results in transcriptional silencing of one X-chromosome in females. X chromosome inactivation (XCI) is random with respect to the parental origin of the X, occurs early during embryonic development, and is then stably maintained through a near infinite number of cell divisions. As a result of this, every female individual consists of a mosaic of two different cell populations, in which either the maternally or paternally derived X-chromosome is inactivated. As the X-chromosome harbors more than a thousand genes, of which many are implicated in human disease when mutated, this mosaicism has important disease implications. Whereas X-linked disorders are usually more severe in hemizygous males harboring a single X-chromosome, a more variable phenotype is observed in females. This variability is a direct consequence of the XCI-mosaicism, and is affected by the randomness of the XCI process. Here we review the latest insights into the regulation of this important female specific process, and discuss mechanisms that influence mosaicism in females, with a focus on the clinical consequences related to X-linked diseases in females.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted March 07, 2017.
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X-chromosome inactivation and its implications for human disease
Joost Gribnau, Tahsin Stefan Barakat
bioRxiv 076950; doi: https://doi.org/10.1101/076950
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X-chromosome inactivation and its implications for human disease
Joost Gribnau, Tahsin Stefan Barakat
bioRxiv 076950; doi: https://doi.org/10.1101/076950

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