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Developmental programming and epigenetics
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DOI：10.3945/ajcn.110.000927.png)
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Abstract
En 中文
The ways in which epigenetic modifications fix the effects of early environmental events, ensuring sustained responses to transient stimuli that result in modified gene expression patterns and phenotypes later in life, are a topic of considerable interest. This article focuses on recently discovered mechanisms and calls into question prevailing views about the dynamics, positions, and functions of epigenetic marks. Most epigenetic studies have addressed the long-term effects of environmental stressors on a small number of epigenetic marks, at the global or individual gene level, in humans and in animal models. In parallel, increasing numbers of studies based on high-throughput technologies are revealing additional complexity in epigenetic processes by highlighting the importance of crosstalk between different epigenetic marks in humans and mice. A number of studies focusing on metabolic programming and the developmental origin of health and disease have identified links between early nutrition, epigenetic processes, and long-term illness. The existence of a self-propagating epigenetic cycle has been shown. Moreover, recent studies have shown an obvious sexual dimorphism both for programming trajectories and in response to the same environmental insult. Despite recent progress, however, we are still far from understanding how, when, and where environmental stressors disturb key epigenetic mechanisms. Thus, the need to identify original key marks and monitor the changes they undergo throughout development, during an individual's lifetime, or over several generations remains a challenging issue. Am J Clin Nutr 2011;94(suppl):1943S-52S.
Keywords:
EMBRYONIC STEM-CELLS
HEPATIC GENE-EXPRESSION
NON-CPG METHYLATION
INTRAUTERINE GROWTH-RETARDATION
INDUCED HISTONE MODIFICATIONS
MATERNAL PROTEIN RESTRICTION
HUMAN CHORIONIC-GONADOTROPIN
FOLIC-ACID SUPPLEMENTATION
RENIN-ANGIOTENSIN SYSTEM
DNA METHYLATION
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