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Journal ArticleDOI

Epigenetic dynamics of imprinted X inactivation during early mouse development.

TLDR
It is shown that although initially active, the paternal X chromosome undergoes imprinted inactivation from the cleavage stages, well before cellular differentiation, which reveals the remarkable plasticity of the X-inactivation process during preimplantation development and underlines the importance of the ICM in global reprogramming of epigenetic marks in the early embryo.
Abstract
The initiation of X-chromosome inactivation is thought to be tightly correlated with early differentiation events during mouse development. Here, we show that although initially active, the paternal X chromosome undergoes imprinted inactivation from the cleavage stages, well before cellular differentiation. A reversal of the inactive state, with a loss of epigenetic marks such as histone modifications and polycomb proteins, subsequently occurs in cells of the inner cell mass (ICM), which give rise to the embryo-proper in which random X inactivation is known to occur. This reveals the remarkable plasticity of the X-inactivation process during preimplantation development and underlines the importance of the ICM in global reprogramming of epigenetic marks in the early embryo.

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Citations
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Journal ArticleDOI

The diverse functions of histone lysine methylation.

TL;DR: Recent advances in understanding of how lysine methylation functions in these diverse biological processes are summarized, and questions that need to be addressed in the future are raised.
Journal ArticleDOI

Stability and flexibility of epigenetic gene regulation in mammalian development

Wolf Reik
- 24 May 2007 - 
TL;DR: During development, cells start in a pluripotent state, from which they can differentiate into many cell types, and progressively develop a narrower potential, and their gene-expression programmes become more defined, restricted and, potentially, 'locked in'.
Journal ArticleDOI

Long noncoding RNAs: past, present, and future.

TL;DR: The current state of knowledge of the lncRNA field is reviewed, discussing what is known about the genomic contexts, biological functions, and mechanisms of action of lncRNAs and how this interest is deeply rooted in biology's longstanding concern with the evolution and function of genomes.
Journal ArticleDOI

Epigenetic reprogramming in mammals

TL;DR: Comparative work demonstrates reprogramming in all mammalian species analysed, but the extent and timing varies, consistent with notable differences between species during preimplantation development.
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Single-cell RNA-seq reveals dynamic, random monoallelic gene expression in mammalian cells.

TL;DR: It is concluded that independent and stochastic allelic transcription generates abundant random monoallelic expression in the mammalian cell.
References
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Journal ArticleDOI

Gene Action in the X -chromosome of the Mouse ( Mus musculus L.)

TL;DR: Ohno and Hauschka1 showed that in female mice one chromosome of mammary carcinoma cells and of normal diploid cells of the ovary, mammary gland and liver was heteropyKnotic and suggested that the so-called sex chromatin was composed of one heteropyknotic X-chromosome.
Journal ArticleDOI

Role of histone H3 lysine 27 methylation in X inactivation.

TL;DR: It is demonstrated that transient recruitment of the Eed-Ezh2 complex to the inactive X chromosome (Xi) occurs during initiation of X inactivation in both extraembryonic and embryonic cells and is accompanied by H3-K27 methylation.
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Requirement for Xist in X chromosome inactivation

TL;DR: Evidence for gene targeting of Xist, the proposed candidate for the X inactivation centre, is provided, and its absolute requirement in the process of X chromosome inactivation is provided.
Journal ArticleDOI

Preferential inactivation of the paternally derived X chromosome in the extraembryonic membranes of the mouse

TL;DR: In an effort to determine the embryonic stage at which the X chromosome initiates differentiation in famale mouse embryos heterozygous for Cattanach's translocaton, it was found that the mosaic composition was consistently biased in extraembryonic membranes, whereas it was not necessarily so in the embryonic body.
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