Department of Psychiatry and Neuroscience Ph.D. Program, University of Utah, Salt Lake City, UT 84108, USA.
Molecular Medicine Program, University of Utah, Salt Lake City, UT 84112, USA.
Int J Mol Sci. 2020 Sep 11;21(18):6649. doi: 10.3390/ijms21186649.
Alcohol use disorder (AUD) exacts an immense toll on individuals, families, and society. Genetic factors determine up to 60% of an individual's risk of developing problematic alcohol habits. Effective AUD prevention and treatment requires knowledge of the genes that predispose people to alcoholism, play a role in alcohol responses, and/or contribute to the development of addiction. As a highly tractable and translatable genetic and behavioral model organism, has proven valuable to uncover important genes and mechanistic pathways that have obvious orthologs in humans and that help explain the complexities of addiction. Vinegar flies exhibit remarkably strong face and mechanistic validity as a model for AUDs, permitting many advancements in the quest to understand human genetic involvement in this disease. These advancements occur via approaches that essentially fall into one of two categories: (1) discovering candidate genes via human genome-wide association studies (GWAS), transcriptomics on post-mortem tissue from AUD patients, or relevant physiological connections, then using reverse genetics in flies to validate candidate genes' roles and investigate their molecular function in the context of alcohol. (2) Utilizing flies to discover candidate genes through unbiased screens, GWAS, quantitative trait locus analyses, transcriptomics, or single-gene studies, then validating their translational role in human genetic surveys. In this review, we highlight the utility of as a model for alcoholism by surveying recent advances in our understanding of human AUDs that resulted from these various approaches. We summarize the genes that are conserved in alcohol-related function between humans and flies. We also provide insight into some advantages and limitations of these approaches. Overall, this review demonstrates how have and can be used to answer important genetic questions about alcohol addiction.
酒精使用障碍(AUD)给个人、家庭和社会带来了巨大的损失。遗传因素决定了个体出现问题性饮酒习惯的风险高达 60%。有效的 AUD 预防和治疗需要了解易导致酗酒的基因、在酒精反应中起作用的基因,以及/或有助于成瘾发展的基因。作为一种高度可行且可转化的遗传和行为模式生物,已经被证明对揭示重要基因和机制途径非常有价值,这些基因和机制途径在人类中有明显的同源物,可以帮助解释成瘾的复杂性。醋蝇作为 AUD 的模型具有非常强的面部和机制有效性,允许在理解人类遗传参与这种疾病方面取得许多进展。这些进展是通过以下两种方法中的一种实现的:(1)通过人类全基因组关联研究(GWAS)、AUD 患者死后组织的转录组学或相关生理联系发现候选基因,然后使用苍蝇中的反向遗传学来验证候选基因的作用,并研究其在酒精背景下的分子功能。(2)利用苍蝇通过无偏筛选、GWAS、数量性状基因座分析、转录组学或单基因研究发现候选基因,然后在人类遗传调查中验证其翻译作用。在这篇综述中,我们通过调查这些方法在理解人类 AUD 方面取得的最新进展,强调了醋蝇作为酒精中毒模型的效用。我们总结了在人类和苍蝇之间与酒精相关功能保守的基因。我们还提供了对这些方法的一些优势和局限性的见解。总的来说,这篇综述表明了 如何以及可以用来回答关于酒精成瘾的重要遗传问题。