Foldi Claire J, Eyles Darryl W, Flatscher-Bader Traute, McGrath John J, Burne Thomas H J
Queensland Brain Institute, The University of Queensland St Lucia, QLD, Australia.
Front Behav Neurosci. 2011 Jun 23;5:32. doi: 10.3389/fnbeh.2011.00032. eCollection 2011.
Offspring of older fathers have an increased risk of various adverse health outcomes, including autism and schizophrenia. With respect to biological mechanisms for this association, there are many more germline cell divisions in the life history of a sperm relative to that of an oocyte. This leads to more opportunities for copy error mutations in germ cells from older fathers. Evidence also suggests that epigenetic patterning in the sperm from older men is altered. Rodent models provide an experimental platform to examine the association between paternal age and brain development. Several rodent models of advanced paternal age (APA) have been published with relevance to intermediate phenotypes related to autism. All four published APA models vary in key features creating a lack of consistency with respect to behavioral phenotypes. A consideration of common phenotypes that emerge from these APA-related mouse models may be informative in the exploration of the molecular and neurobiological correlates of APA.
年长父亲的后代出现各种不良健康结局的风险会增加,包括自闭症和精神分裂症。关于这种关联的生物学机制,相对于卵母细胞,精子的生命历程中有更多的生殖系细胞分裂。这导致年长父亲的生殖细胞中出现复制错误突变的机会更多。证据还表明,年长男性精子中的表观遗传模式会发生改变。啮齿动物模型提供了一个实验平台,用于研究父亲年龄与大脑发育之间的关联。已经发表了几种与自闭症相关中间表型有关的高龄父亲(APA)啮齿动物模型。所有已发表的四种APA模型在关键特征上各不相同,在行为表型方面缺乏一致性。考虑这些与APA相关的小鼠模型中出现的共同表型,可能有助于探索APA的分子和神经生物学相关性。