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Journal ArticleDOI

Epigenetic events in mammalian germ-cell development: reprogramming and beyond

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TLDR
It is shown that epigenetic modifiers have key roles in germ-cell development itself and contributes to the gene-expression programme that is required for germ- cell development, regulation of meiosis and genomic integrity.
Abstract
The epigenetic profile of germ cells, which is defined by modifications of DNA and chromatin, changes dynamically during their development. Many of the changes are associated with the acquisition of the capacity to support post-fertilization development. Our knowledge of this aspect has greatly increased- for example, insights into how the re-establishment of parental imprints is regulated. In addition, an emerging theme from recent studies is that epigenetic modifiers have key roles in germ-cell development itself--for example, epigenetics contributes to the gene-expression programme that is required for germ-cell development, regulation of meiosis and genomic integrity. Understanding epigenetic regulation in germ cells has implications for reproductive engineering technologies and human health.

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Journal ArticleDOI

The Enzymatic Decarboxylation Mechanism of 5-Carboxy Uracil: A Comprehensive Quantum Chemical Study.

TL;DR: In this article, the authors employ quantum chemical and molecular mechanic calculations and find that the catalytic mechanism of IDCase proceeds via a direct decarboxylation mechanism, which is a one-step mechanism with concerted proton transfer and C-C bond opening.
Reference EntryDOI

Pharmaco‐Epigenomics to Improve Cancer Therapies

TL;DR: In this chapter, the recent advances in the field of pharmaco-epigenomics will be highlighted, and a review included of the most recently discovered and promising epigenetic therapies and biomarkers aimed at improving cancer diagnosis and treatment.
Journal ArticleDOI

Genomic imprinting in human placentation

TL;DR: Genomic imprinting (GI) is a mammalian-specific epigenetic phenomenon that has been implicated in the evolution of the placenta in mammals as mentioned in this paper , and it has been shown to be a powerful mechanism for gene expression.
References
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Journal ArticleDOI

A Bivalent Chromatin Structure Marks Key Developmental Genes in Embryonic Stem Cells

TL;DR: It is proposed that bivalent domains silence developmental genes in ES cells while keeping them poised for activation, highlighting the importance of DNA sequence in defining the initial epigenetic landscape and suggesting a novel chromatin-based mechanism for maintaining pluripotency.
Journal ArticleDOI

Generation of germline-competent induced pluripotent stem cells

TL;DR: iPS cells competent for germline chimaeras can be obtained from fibroblasts, but retroviral introduction of c-Myc should be avoided for clinical application.
Journal ArticleDOI

In vitro reprogramming of fibroblasts into a pluripotent ES-cell-like state

TL;DR: The results show that the biological potency and epigenetic state of in-vitro-reprogrammed induced pluripotent stem cells are indistinguishable from those of ES cells.
Journal ArticleDOI

Epigenetic Transgenerational Actions of Endocrine Disruptors and Male Fertility

TL;DR: The ability of an environmental factor to reprogram the germ line and to promote a transgenerational disease state has significant implications for evolutionary biology and disease etiology.
Journal ArticleDOI

Environmental epigenomics and disease susceptibility.

TL;DR: An increasing body of evidence from animal studies supports the role of environmental epigenetics in disease susceptibility and recent studies have demonstrated for the first time that heritable environmentally induced epigenetic modifications underlie reversible transgenerational alterations in phenotype.
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