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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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Citations
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Journal ArticleDOI

Active DNA demethylation in mammals

TL;DR: It is described that active DNA demethylation take place in a spatial- and temporal-specific way on the basis of recent literatures and several candidate pathways such as oxygenation and deamination of 5-methyl cytosine and DNA repair pathways, which may be responsible for the active process were introduced on a cell- and tissue-specific view.
Journal ArticleDOI

Epigenetics: Getting to the roots of mammalian imprinting

TL;DR: The findings suggest that, contrary to previous theories, imprinting by germlinederived methylation evolved before the advent of therian mammals, as did the regulation of imprinted-gene clusters by mechanisms controlling a whole domain.
Journal ArticleDOI

Effects of tributyltin chloride on developing mouse oocytes and preimplantation embryos.

TL;DR: The results suggest that TBTCl induces developmental defects in oocytes and preimplantation embryos and tributyltin chloride is an endocrine disruptor in many wildlife species.
Book ChapterDOI

Development of Artificial Gametes

TL;DR: This chapter aims to provide an updated and broad review about the biological progress of artificial gamete production, considering especially different sources of stem cells, animal models and the potential production of artificial human gametes in vitro.
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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