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Paternal Diet Defines Offspring Chromatin State and Intergenerational Obesity

机译:父亲的饮食定义了后代染色质状态和代际肥胖

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The global rise in obesity has revitalized a search for genetic and epigenetic factors underlying the disease. We present a Drosophila model of paternal-diet-induced intergenerational metabolic reprogramming (IGMR) and identify genes required for its encoding in offspring. Intriguingly, we find that as little as 2 days of dietary intervention in fathers elicits obesity in offspring. Paternal sugar acts as a physiological suppressor of variegation, desilencing chromatin-state-defined domains in both mature sperm and in offspring embryos. We identify requirements for H3K9/K27me3-dependent reprogramming of metabolic genes in two distinct germline and zygotic windows. Critically, we find evidence that a similar system may regulate obesity susceptibility and phenotype variation in mice and humans. The findings provide insight into the mechanisms underlying intergenerational metabolic reprogramming and carry profound implications for our understanding of phenotypic variation and evolution.
机译:肥胖症的全球上升使寻找该疾病的遗传和表观遗传因素成为可能。我们提出了果蝇模型的父亲节食诱导代际代谢重编程(IGMR),并确定其后代编码所需的基因。有趣的是,我们发现,父亲进行饮食干预仅2天即可引起后代肥胖。父糖可作为杂色的生理抑制物,使成熟精子和后代胚胎中的染色质状态定义域沉默。我们确定两个不同的种系和合子窗口中的代谢基因的H3K9 / K27me3依赖性重编程的要求。至关重要的是,我们发现证据表明,类似的系统可能会调节小鼠和人类的肥胖易感性和表型变异。这些发现提供了对代际代谢重编程基础机制的深入了解,并为我们对表型变异和进化的理解带来了深刻的启示。

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