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首页> 外文期刊>Journal of developmental origins of health and disease >Epigenetic studies in Developmental Origins of Health and Disease: pitfalls and key considerations for study design and interpretation
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Epigenetic studies in Developmental Origins of Health and Disease: pitfalls and key considerations for study design and interpretation

机译:健康疾病发育起源的表观遗传研究:陷阱与研究设计与解释的关键因素

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The field of Developmental Origins of Health and Disease (DOHaD) seeks to understand the relationships between early-life environmental exposures and long-term health and disease. Until recently, the molecular mechanisms underlying these phenomena were poorly understood; however, epigenetics has been proposed to bridge the gap between the environment and phenotype. Epigenetics involves the study of heritable changes in gene expression, which occur without changes to the underlying DNA sequence. Different types of epigenetic modifications include DNA methylation, post-translational histone modifications and non-coding RNAs. Increasingly, changes to the epigenome have been associated with early-life exposures in both humans and animal models, offering both an explanation for how the environment may programme long-term health, as well as molecular changes that could be developed as biomarkers of exposure and/or future disease. As such, epigenetic studies in DOHaD hold much promise; however, there are a number of factors which should be considered when designing and interpreting such studies. These include the impact of the genome on the epigenome, the tissue-specificity of epigenetic marks, the stability (or lack thereof) of epigenetic changes over time and the importance of associating epigenetic changes with changes in transcription or translation to demonstrate functional consequences. In this review, we discuss each of these key concepts and provide practical strategies to mitigate some common pitfalls with the aim of providing a useful guide for future epigenetic studies in DOHaD.
机译:健康和疾病的发育起源领域(多哈德)寻求了解早期环境暴露和长期健康和疾病之间的关系。直到最近,这些现象的分子机制尚未理解;然而,已经提出了表观遗传学来弥合了环境与表型之间的差距。表观遗传学涉及基因表达的遗传变化的研究,这不会发生底层DNA序列。不同类型的表观遗传修饰包括DNA甲基化,翻译后组蛋白修饰和非编码RNA。越来越多地,对外延蛋白组的变化已经与人类和动物模型中的早期风险有关,提供了对环境如何规划长期健康的解释,以及可以作为暴露的生物标志物开发的分子变化/或未来的疾病。因此,杜地面的表观遗传研究占据了许多承诺;然而,在设计和解释这些研究时,应该考虑许多因素。这些包括基因组对表观群组织的影响,表观遗传标记的组织特异性表观遗传痕迹随时间的变化以及与转录或翻译变化相关联的表观遗传变化的重要性,以证明功能后果。在这篇综述中,我们讨论了这些关键概念中的每一个,并提供了减轻一些普通陷阱的实际策略,目的是为未来的诺哈德进行有用的表观遗传研究指南。

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