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The Probability to Initiate X Chromosome Inactivation Is Determined by the X to Autosomal Ratio and X Chromosome Specific Allelic Properties

BACKGROUND: In female mammalian cells, random X chromosome inactivation (XCI) equalizes the dosage of X-encoded gene products to that in male cells. XCI is a stochastic process, in which each X chromosome has a probability to be inactivated. To obtain more insight in the factors setting up this prob...

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Autores principales: Monkhorst, Kim, de Hoon, Bas, Jonkers, Iris, Mulugeta Achame, Eskeatnaf, Monkhorst, Wouter, Hoogerbrugge, Jos, Rentmeester, Eveline, Westerhoff, Hans V., Grosveld, Frank, Grootegoed, J. Anton, Gribnau, Joost
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2680018/
https://www.ncbi.nlm.nih.gov/pubmed/19440388
http://dx.doi.org/10.1371/journal.pone.0005616
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author Monkhorst, Kim
de Hoon, Bas
Jonkers, Iris
Mulugeta Achame, Eskeatnaf
Monkhorst, Wouter
Hoogerbrugge, Jos
Rentmeester, Eveline
Westerhoff, Hans V.
Grosveld, Frank
Grootegoed, J. Anton
Gribnau, Joost
author_facet Monkhorst, Kim
de Hoon, Bas
Jonkers, Iris
Mulugeta Achame, Eskeatnaf
Monkhorst, Wouter
Hoogerbrugge, Jos
Rentmeester, Eveline
Westerhoff, Hans V.
Grosveld, Frank
Grootegoed, J. Anton
Gribnau, Joost
author_sort Monkhorst, Kim
collection PubMed
description BACKGROUND: In female mammalian cells, random X chromosome inactivation (XCI) equalizes the dosage of X-encoded gene products to that in male cells. XCI is a stochastic process, in which each X chromosome has a probability to be inactivated. To obtain more insight in the factors setting up this probability, we studied the role of the X to autosome (X∶A) ratio in initiation of XCI, and have used the experimental data in a computer simulation model to study the cellular population dynamics of XCI. METHODOLOGY/PRINCIPAL FINDINGS: To obtain more insight in the role of the X∶A ratio in initiation of XCI, we generated triploid mouse ES cells by fusion of haploid round spermatids with diploid female and male ES cells. These fusion experiments resulted in only XXY triploid ES cells. XYY and XXX ES lines were absent, suggesting cell death related either to insufficient X-chromosomal gene dosage (XYY) or to inheritance of an epigenetically modified X chromosome (XXX). Analysis of active (Xa) and inactive (Xi) X chromosomes in the obtained triploid XXY lines indicated that the initiation frequency of XCI is low, resulting in a mixed population of XaXiY and XaXaY cells, in which the XaXiY cells have a small proliferative advantage. This result, and findings on XCI in diploid and tetraploid ES cell lines with different X∶A ratios, provides evidence that the X∶A ratio determines the probability for a given X chromosome to be inactivated. Furthermore, we found that the kinetics of the XCI process can be simulated using a probability for an X chromosome to be inactivated that is proportional to the X∶A ratio. These simulation studies re-emphasize our hypothesis that the probability is a function of the concentration of an X-encoded activator of XCI, and of X chromosome specific allelic properties determining the threshold for this activator. CONCLUSIONS: The present findings reveal that the probability for an X chromosome to be inactivated is proportional to the X∶A ratio. This finding supports the presence of an X-encoded activator of the XCI process.
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spelling pubmed-26800182009-05-18 The Probability to Initiate X Chromosome Inactivation Is Determined by the X to Autosomal Ratio and X Chromosome Specific Allelic Properties Monkhorst, Kim de Hoon, Bas Jonkers, Iris Mulugeta Achame, Eskeatnaf Monkhorst, Wouter Hoogerbrugge, Jos Rentmeester, Eveline Westerhoff, Hans V. Grosveld, Frank Grootegoed, J. Anton Gribnau, Joost PLoS One Research Article BACKGROUND: In female mammalian cells, random X chromosome inactivation (XCI) equalizes the dosage of X-encoded gene products to that in male cells. XCI is a stochastic process, in which each X chromosome has a probability to be inactivated. To obtain more insight in the factors setting up this probability, we studied the role of the X to autosome (X∶A) ratio in initiation of XCI, and have used the experimental data in a computer simulation model to study the cellular population dynamics of XCI. METHODOLOGY/PRINCIPAL FINDINGS: To obtain more insight in the role of the X∶A ratio in initiation of XCI, we generated triploid mouse ES cells by fusion of haploid round spermatids with diploid female and male ES cells. These fusion experiments resulted in only XXY triploid ES cells. XYY and XXX ES lines were absent, suggesting cell death related either to insufficient X-chromosomal gene dosage (XYY) or to inheritance of an epigenetically modified X chromosome (XXX). Analysis of active (Xa) and inactive (Xi) X chromosomes in the obtained triploid XXY lines indicated that the initiation frequency of XCI is low, resulting in a mixed population of XaXiY and XaXaY cells, in which the XaXiY cells have a small proliferative advantage. This result, and findings on XCI in diploid and tetraploid ES cell lines with different X∶A ratios, provides evidence that the X∶A ratio determines the probability for a given X chromosome to be inactivated. Furthermore, we found that the kinetics of the XCI process can be simulated using a probability for an X chromosome to be inactivated that is proportional to the X∶A ratio. These simulation studies re-emphasize our hypothesis that the probability is a function of the concentration of an X-encoded activator of XCI, and of X chromosome specific allelic properties determining the threshold for this activator. CONCLUSIONS: The present findings reveal that the probability for an X chromosome to be inactivated is proportional to the X∶A ratio. This finding supports the presence of an X-encoded activator of the XCI process. Public Library of Science 2009-05-19 /pmc/articles/PMC2680018/ /pubmed/19440388 http://dx.doi.org/10.1371/journal.pone.0005616 Text en Monkhorst et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Monkhorst, Kim
de Hoon, Bas
Jonkers, Iris
Mulugeta Achame, Eskeatnaf
Monkhorst, Wouter
Hoogerbrugge, Jos
Rentmeester, Eveline
Westerhoff, Hans V.
Grosveld, Frank
Grootegoed, J. Anton
Gribnau, Joost
The Probability to Initiate X Chromosome Inactivation Is Determined by the X to Autosomal Ratio and X Chromosome Specific Allelic Properties
title The Probability to Initiate X Chromosome Inactivation Is Determined by the X to Autosomal Ratio and X Chromosome Specific Allelic Properties
title_full The Probability to Initiate X Chromosome Inactivation Is Determined by the X to Autosomal Ratio and X Chromosome Specific Allelic Properties
title_fullStr The Probability to Initiate X Chromosome Inactivation Is Determined by the X to Autosomal Ratio and X Chromosome Specific Allelic Properties
title_full_unstemmed The Probability to Initiate X Chromosome Inactivation Is Determined by the X to Autosomal Ratio and X Chromosome Specific Allelic Properties
title_short The Probability to Initiate X Chromosome Inactivation Is Determined by the X to Autosomal Ratio and X Chromosome Specific Allelic Properties
title_sort probability to initiate x chromosome inactivation is determined by the x to autosomal ratio and x chromosome specific allelic properties
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2680018/
https://www.ncbi.nlm.nih.gov/pubmed/19440388
http://dx.doi.org/10.1371/journal.pone.0005616
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