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Glypican Gene GPC5 Participates in the Behavioral Response to Ethanol: Evidence from Humans Mice and Fruit Flies

机译:Glypican基因GPC5参与乙醇的行为响应:来自人类小鼠和果蝇的证据

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摘要

Alcohol use disorders are influenced by many interacting genetic and environmental factors. Highlighting this complexity is the observation that large genome-wide association experiments have implicated many genes with weak statistical support. Experimental model systems, cell culture and animal, have identified many genes and pathways involved in ethanol response, but their applicability to the development of alcohol use disorders in humans is undetermined. To overcome the limitations of any single experimental system, the analytical strategy used here was to identify genes that exert common phenotypic effects across multiple experimental systems. Specifically, we (1) performed a mouse linkage analysis to identify quantitative trait loci that influence ethanol-induced ataxia; (2) performed a human genetic association analysis of the mouse-identified loci against ethanol-induced body sway, a phenotype that is not only comparable to the mouse ethanol-ataxia phenotype but is also a genetically influenced endophenotype of alcohol use disorders; (3) performed behavioral genetic experiments in Drosophila showing that fly homologs of GPC5, the member of the glypican gene family implicated by both the human and mouse genetic analyses, influence the fly’s response to ethanol; and (4) discovered data from the literature demonstrating that the genetically implicated gene’s expression is not only temporally and spatially consistent with involvement in ethanol-induced behaviors but is also modulated by ethanol. The convergence of these data provides strong support to the hypothesis that GPC5 is involved in cellular and organismal ethanol response and the etiology of alcohol use disorders in humans.
机译:酒精使用障碍会受到许多相互作用的遗传和环境因素的影响。突出这一复杂性的发现是,大型全基因组关联实验牵涉到许多基因的统计支持较弱。实验模型系统,细胞培养和动物实验已经确定了许多与乙醇反应有关的基因和途径,但它们在人类酒精使用障碍发展中的适用性尚未确定。为了克服任何单个实验系统的局限性,此处使用的分析策略是鉴定在多个实验系统中发挥共同表型效应的基因。具体来说,我们(1)进行了小鼠连锁分析,以识别影响乙醇诱导的共济失调的数量性状基因座; (2)对小鼠识别的基因座针对乙醇诱导的身体摇摆进行了人类遗传关联分析,该表型不仅与小鼠乙醇共济失调表型相当,而且还是酒精使用障碍的遗传影响内表型; (3)在果蝇中进行了行为遗传实验,结果表明,人和小鼠的基因分析均牵涉Glypican基因家族成员GPC5的果蝇同源物,影响果蝇对乙醇的反应; (4)从文献中发现的数据表明,遗传相关基因的表达不仅在时间和空间上与参与乙醇诱导的行为有关,而且还受到乙醇的调节。这些数据的融合为GPC5参与细胞和生物乙醇反应以及人类饮酒障碍的病因的假设提供了有力的支持。

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