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Early-Life Stress Induced Epigenetic Changes of Corticotropin-Releasing Factor Gene in Anorexic Low Body Weight–Selected Chicks

机译:早期应激诱导的厌食症低体重小鸡中促肾上腺皮质激素释放因子基因的表观遗传变化

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摘要

The expression of neuropeptide Y ( ) in the arcuate nucleus (ARC) and corticotropin-releasing factor ( ) in the paraventricular nucleus (PVN) were increased when low body weight–selected (LWS) line chicks, which are predisposed to anorexia, were subjected to a combination of nutritional and thermal stressors at hatch. We hypothesized that such changes resulted from epigenetic modifications. We determined global DNA methylation, DNA methyltransferase (DNMT) activity, and methylation near the promoter regions of and , in the hypothalamus of LWS chicks on day 5 post-hatch. Stress exposure at hatch induced global hypermethylation and increased DNMT activity in the ARC but not PVN. In the PVN of stressed LWS chicks, there was decreased methylation of a CpG site located at the core binding domain of methyl cytosine binding domain protein 2 (MBD2), near the gene promoter. We then demonstrated that this was associated with disrupted binding of MBD2. There was also reduced utilization of yolk reserves and lean and fat masses in chicks that were stress-exposed. These findings provide novel insights on molecular mechanisms through which stressful events induce or intensify anorexia in predisposed individuals and a novel molecular target for further studies.
机译:当对易患厌食症的低体重选择(LWS)系雏鸡进行弓形核(ARC)中神经肽Y()的表达和室旁核(PVN)中促肾上腺皮质激素释放因子()的表达会增加孵化时要结合营养和热应激因素。我们假设这种变化是由表观遗传修饰引起的。在孵化后第5天,我们确定了LWS雏鸡下丘脑的全局DNA甲基化,DNA甲基转移酶(DNMT)活性和的启动子区域附近的甲基化。孵化中的应力暴露会导致ARC中的全局过度甲基化并增加DNMT活性,但不会引起PVN。在应激的LWS雏鸡的PVN中,位于基因启动子附近的甲基胞嘧啶结合域蛋白2(MBD2)核心结合域的CpG位点的甲基化降低。然后,我们证明了这与MBD2的结合破坏有关。压力暴露的雏鸡的蛋黄储备和瘦肉和脂肪量的利用率也降低了。这些发现提供了有关分子机制的新颖见解,通过该机制应激事件可诱发或加剧易感个体的厌食症,并为进一步研究提供了新的分子靶标。

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