Yauk Carole L, Lambert Iain B, Meek M E Bette, Douglas George R, Marchetti Francesco
Environmental Health Science and Research Bureau, Health Canada, Ottawa, Ontario, Canada.
Department of Biology, Carleton University, Ottawa, Ontario, Canada.
Environ Mol Mutagen. 2015 Dec;56(9):724-50. doi: 10.1002/em.21954. Epub 2015 May 22.
The Organisation for Economic Cooperation and Development's (OECD) Adverse Outcome Pathway (AOP) programme aims to develop a knowledgebase of all known pathways of toxicity that lead to adverse effects in humans and ecosystems. A Users' Handbook was recently released to provide supplementary guidance on AOP development. This article describes one AOP-alkylation of DNA in male premeiotic germ cells leading to heritable mutations. This outcome is an important regulatory endpoint. The AOP describes the biological plausibility and empirical evidence supporting that compounds capable of alkylating DNA cause germ cell mutations and subsequent mutations in the offspring of exposed males. Alkyl adducts are subject to DNA repair; however, at high doses the repair machinery becomes saturated. Lack of repair leads to replication of alkylated DNA and ensuing mutations in male premeiotic germ cells. Mutations that do not impair spermatogenesis persist and eventually are present in mature sperm. Thus, the mutations are transmitted to the offspring. Although there are some gaps in empirical support and evidence for essentiality of the key events for certain aspects of this AOP, the overall AOP is generally accepted as dogma and applies broadly to any species that produces sperm. The AOP was developed and used in an iterative process to test and refine the Users' Handbook, and is one of the first publicly available AOPs. It is our hope that this AOP will be leveraged to develop other AOPs in this field to advance method development, computational models to predict germ cell effects, and integrated testing strategies.
经济合作与发展组织(OECD)的不良结局途径(AOP)计划旨在建立一个知识库,涵盖所有已知的导致对人类和生态系统产生不良影响的毒性途径。最近发布了一本用户手册,为AOP的开发提供补充指导。本文描述了一种导致可遗传突变的AOP——雄性减数分裂前生殖细胞中DNA的烷基化。这一结果是一个重要的监管终点。该AOP描述了生物学合理性和实证证据,支持能够烷基化DNA的化合物会导致生殖细胞突变以及暴露雄性后代中的后续突变。烷基加合物会进行DNA修复;然而,在高剂量下,修复机制会饱和。缺乏修复会导致烷基化DNA的复制以及雄性减数分裂前生殖细胞中随之而来的突变。不损害精子发生的突变会持续存在,并最终存在于成熟精子中。因此,这些突变会传递给后代。尽管在实证支持以及该AOP某些方面关键事件的必要性证据方面存在一些差距,但总体而言,该AOP被广泛接受为准则,并广泛适用于任何产生精子的物种。该AOP是在一个迭代过程中开发和使用的,以测试和完善用户手册,并且是首批公开可用的AOP之一。我们希望利用这个AOP来开发该领域的其他AOP,以推进方法开发、预测生殖细胞效应的计算模型以及综合测试策略。