Abstract

X-chromosome inactivation (XCI) is a developmental process that aims to equalize the dosage of X-linked gene products between XY males and XX females in eutherian mammals. In female mouse embryos, paternal XCI is initiated at the 4-cell stage; however, the X chromosome is reactivated in the inner cell mass cells of blastocysts, and random XCI is subsequently initiated in epiblast cells. However, recent findings show that the patterns of XCI are not conserved among mammals. In this study, we used quantitative RT-PCR and RNA in situ hybridization combined with immunofluorescence to investigate the pattern of XCI during bovine embryo development. Expression of XIST (X-inactive specific transcript) RNA was significantly upregulated at the morula stage. For the first time, we demonstrate that XIST accumulation in bovine embryos starts in nuclei of female morulae, but its colocalization with histone H3 lysine 27 trimethylation was first detected in day 7 blastocysts. Both in the inner cell mass and in putative epiblast precursors, we observed a proportion of cells with XIST RNA and H3K27me3 colocalization. Surprisingly, the onset of XCI did not lead to a global downregulation of X-linked genes, even in day 9 blastocysts. Together, our findings confirm that diverse patterns of XCI initiation exist among developing mammalian embryos.

Highlights

  • In placental mammals, dosage compensation for X-encoded genes between female (XX) and male (XY) cells is achieved by inactivation of one of the two X chromosomes in female cells

  • HPRT1 is an X-linked gene known to be inactivated after X-chromosome inactivation (XCI); its downregulation has been proposed as a marker for XCI [25,26]

  • These data suggest that XCI expression starts around the morula stage in bovine embryos

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Summary

Introduction

Dosage compensation for X-encoded genes between female (XX) and male (XY) cells is achieved by inactivation of one of the two X chromosomes in female cells. To silence the chromatin and repress the X-linked genes from that chromosome, XIST recruits epigenetic modifiers [3]. In the mouse, imprinted XCI is initiated at the 4-cell stage embryo stage with exclusive inactivation of the paternal X chromosome (Xp). The paternal X chromosome remains inactive in trophectoderm (TE) cells during and after formation of the mouse blastocyst [6,7]. In the inner cell mass (ICM) of female embryos, the inactive Xp is reactivated, resulting in two active X

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