Mokashi Sneha S, Shankar Vijay, MacPherson Rebecca A, Hannah Rachel C, Mackay Trudy F C, Anholt Robert R H
Department of Genetics and Biochemistry and Center for Human Genetics, Clemson University, Greenwood, SC, United States.
Front Psychiatry. 2021 Jul 22;12:699033. doi: 10.3389/fpsyt.2021.699033. eCollection 2021.
Fetal alcohol exposure can lead to developmental abnormalities, intellectual disability, and behavioral changes, collectively termed fetal alcohol spectrum disorder (FASD). In 2015, the Centers for Disease Control found that 1 in 10 pregnant women report alcohol use and more than 3 million women in the USA are at risk of exposing their developing fetus to alcohol. is an excellent genetic model to study developmental effects of alcohol exposure because many individuals of the same genotype can be reared rapidly and economically under controlled environmental conditions. Flies exposed to alcohol undergo physiological and behavioral changes that resemble human alcohol-related phenotypes. Here, we show that adult flies that developed on ethanol-supplemented medium have decreased viability, reduced sensitivity to ethanol, and disrupted sleep and activity patterns. To assess the effects of exposure to alcohol during development on brain gene expression, we performed single cell RNA sequencing and resolved cell clusters with differentially expressed genes which represent distinct neuronal and glial populations. Differential gene expression showed extensive sexual dimorphism with little overlap between males and females. Gene expression differences following developmental alcohol exposure were similar to previously reported differential gene expression following cocaine consumption, suggesting that common neural substrates respond to both drugs. Genes associated with glutathione metabolism, lipid transport, glutamate and GABA metabolism, and vision feature in sexually dimorphic global multi-cluster interaction networks. Our results provide a blueprint for translational studies on alcohol-induced effects on gene expression in the brain that may contribute to or result from FASD in human populations.
胎儿酒精暴露可导致发育异常、智力残疾和行为改变,统称为胎儿酒精谱系障碍(FASD)。2015年,疾病控制中心发现,每10名孕妇中有1人报告饮酒,美国有超过300万妇女面临将发育中的胎儿暴露于酒精的风险。果蝇是研究酒精暴露发育影响的优秀遗传模型,因为许多相同基因型的个体可以在受控环境条件下快速且经济地饲养。暴露于酒精的果蝇会经历生理和行为变化,这些变化类似于人类与酒精相关的表型。在这里,我们表明在添加乙醇的培养基上发育的成年果蝇活力下降、对乙醇的敏感性降低,睡眠和活动模式受到干扰。为了评估发育过程中酒精暴露对大脑基因表达的影响,我们进行了单细胞RNA测序,并解析了具有差异表达基因的细胞簇,这些基因代表不同的神经元和神经胶质细胞群体。差异基因表达显示出广泛的性别二态性,雄性和雌性之间几乎没有重叠。发育性酒精暴露后的基因表达差异与先前报道的可卡因摄入后的差异基因表达相似,这表明常见的神经底物对这两种药物都有反应。与谷胱甘肽代谢、脂质转运、谷氨酸和γ-氨基丁酸代谢以及视觉相关的基因在性别二态性全局多簇相互作用网络中具有特征。我们的结果为酒精对大脑基因表达的诱导作用的转化研究提供了蓝图,这些作用可能导致人类群体中的FASD或由其导致。