Abstract

BackgroundIn 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 FindingsTo 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.ConclusionsThe 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.

Highlights

  • In placental mammals, dosage compensation of X-encoded gene products is achieved by inactivation of either of the two X chromosomes in female cells [1]

  • The present findings reveal that the probability for an X chromosome to be inactivated is proportional to the X:A ratio

  • Generation of triploid embryonic stem (ES) cells Our previous studies with tetraploid XXXX, XXXY and XXYY mouse ES cell lines have indicated that the probability for an X chromosome to be inactivated is directly related to the X:A ratio [10]

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Summary

Introduction

Dosage compensation of X-encoded gene products is achieved by inactivation of either of the two X chromosomes in female cells [1]. Random X chromosome inactivation (XCI) is initiated early during female embryonic development, and results in a transcriptionally inactive X chromosome (Xi). The Tsix and Xite genes play a crucial role in the early stages of XCI by suppression of Xist transcription and Xist RNA accumulation. Both Tsix and Xite are non-coding genes that overlap with Xist, but are transcribed in anti-sense direction [8,9]. Random X chromosome inactivation (XCI) equalizes the dosage of X-encoded gene products to that in male cells. 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

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