Tyler A L, McGarr T C, Beyer B J, Frankel W N, Carter G W
The Jackson Laboratory, Bar Harbor, ME, USA.
Genes Brain Behav. 2014 Nov;13(8):831-40. doi: 10.1111/gbb.12178. Epub 2014 Oct 27.
Absence epilepsy (AE) is a complex, heritable disease characterized by a brief disruption of normal behavior and accompanying spike-wave discharges (SWD) on the electroencephalogram. Only a handful of genes has been definitively associated with AE in humans and rodent models. Most studies suggest that genetic interactions play a large role in the etiology and severity of AE, but mapping and understanding their architecture remains a challenge, requiring new computational approaches. Here we use combined analysis of pleiotropy and epistasis (CAPE) to detect and interpret genetic interactions in a meta-population derived from three C3H × B6J strain crosses, each of which is fixed for a different SWD-causing mutation. Although each mutation causes SWD through a different molecular mechanism, the phenotypes caused by each mutation are exacerbated on the C3H genetic background compared with B6J, suggesting common modifiers. By combining information across two phenotypic measures - SWD duration and frequency - CAPE showed a large, directed genetic network consisting of suppressive and enhancing interactions between loci on 10 chromosomes. These results illustrate the power of CAPE in identifying novel modifier loci and interactions in a complex neurological disease, toward a more comprehensive view of its underlying genetic architecture.
失神癫痫(AE)是一种复杂的遗传性疾病,其特征是正常行为短暂中断,并伴有脑电图上的棘慢波放电(SWD)。在人类和啮齿动物模型中,只有少数基因与AE有明确关联。大多数研究表明,基因相互作用在AE的病因和严重程度中起很大作用,但绘制和理解它们的结构仍然是一项挑战,需要新的计算方法。在这里,我们使用多效性和上位性联合分析(CAPE)来检测和解释来自三个C3H×B6J品系杂交的亚群体中的基因相互作用,每个杂交品系都固定了一个不同的导致SWD的突变。尽管每个突变通过不同的分子机制导致SWD,但与B6J相比,每个突变在C3H遗传背景上引起的表型都更严重,这表明存在共同的修饰基因。通过整合两个表型指标——SWD持续时间和频率——的信息,CAPE显示出一个由10条染色体上基因座之间的抑制和增强相互作用组成的大型定向遗传网络。这些结果说明了CAPE在识别复杂神经疾病中的新修饰基因座和相互作用方面的能力,有助于更全面地了解其潜在的遗传结构。