Montgomery Sara L, Vorojeikina Daria, Huang Wen, Mackay Trudy F C, Anholt Robert R H, Rand Matthew D
Department of Environmental Medicine, University of Rochester School of Medicine and Dentistry, Rochester, New York, United States of America.
Department of Biological Sciences, Genetics Program, and W. M. Keck Center for Behavioral Biology, North Carolina State University, Raleigh, North Carolina, United States of America.
PLoS One. 2014 Oct 31;9(10):e110375. doi: 10.1371/journal.pone.0110375. eCollection 2014.
Methylmercury (MeHg) is a persistent environmental toxin present in seafood that can compromise the developing nervous system in humans. The effects of MeHg toxicity varies among individuals, despite similar levels of exposure, indicating that genetic differences contribute to MeHg susceptibility. To examine how genetic variation impacts MeHg tolerance, we assessed developmental tolerance to MeHg using the sequenced, inbred lines of the Drosophila melanogaster Genetic Reference Panel (DGRP). We found significant genetic variation in the effects of MeHg on development, measured by eclosion rate, giving a broad sense heritability of 0.86. To investigate the influence of dietary factors, we measured MeHg toxicity with caffeine supplementation in the DGRP lines. We found that caffeine counteracts the deleterious effects of MeHg in the majority of lines, and there is significant genetic variance in the magnitude of this effect, with a broad sense heritability of 0.80. We performed genome-wide association (GWA) analysis for both traits, and identified candidate genes that fall into several gene ontology categories, with enrichment for genes involved in muscle and neuromuscular development. Overexpression of glutamate-cysteine ligase, a MeHg protective enzyme, in a muscle-specific manner leads to a robust rescue of eclosion of flies reared on MeHg food. Conversely, mutations in kirre, a pivotal myogenic gene identified in our GWA analyses, modulate tolerance to MeHg during development in accordance with kirre expression levels. Finally, we observe disruptions of indirect flight muscle morphogenesis in MeHg-exposed pupae. Since the pathways for muscle development are evolutionarily conserved, it is likely that the effects of MeHg observed in Drosophila can be generalized across phyla, implicating muscle as an additional hitherto unrecognized target for MeHg toxicity. Furthermore, our observations that caffeine can ameliorate the toxic effects of MeHg show that nutritional factors and dietary manipulations may offer protection against the deleterious effects of MeHg exposure.
甲基汞(MeHg)是一种存在于海鲜中的持久性环境毒素,会损害人类发育中的神经系统。尽管个体接触甲基汞的水平相似,但其毒性影响因人而异,这表明基因差异会导致个体对甲基汞的易感性。为了研究基因变异如何影响对甲基汞的耐受性,我们使用果蝇遗传参考面板(DGRP)的测序近交系评估了对甲基汞的发育耐受性。我们发现甲基汞对发育的影响存在显著的基因变异,以羽化率衡量,广义遗传力为0.86。为了研究饮食因素的影响,我们在DGRP品系中通过添加咖啡因来测量甲基汞的毒性。我们发现咖啡因在大多数品系中可抵消甲基汞的有害影响,并且这种影响的程度存在显著的基因方差,广义遗传力为0.80。我们对这两个性状进行了全基因组关联(GWA)分析,并确定了属于几个基因本体类别的候选基因,其中参与肌肉和神经肌肉发育的基因富集。以肌肉特异性方式过表达甲基汞保护酶谷氨酸 - 半胱氨酸连接酶,可显著挽救在含甲基汞食物上饲养的果蝇的羽化。相反,我们在GWA分析中鉴定出的关键生肌基因kirre中的突变,根据kirre表达水平调节发育过程中对甲基汞的耐受性。最后,我们观察到暴露于甲基汞的蛹中间接飞行肌形态发生受到破坏。由于肌肉发育途径在进化上是保守 的,因此在果蝇中观察到的甲基汞影响可能在整个门中具有普遍性,这意味着肌肉是甲基汞毒性迄今未被认识的另一个靶点。此外,我们观察到咖啡因可以改善甲基汞的毒性作用,这表明营养因素和饮食操作可能提供针对甲基汞暴露有害影响的保护。