The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, UK.
Am J Hum Genet. 2013 May 2;92(5):696-706. doi: 10.1016/j.ajhg.2013.03.019. Epub 2013 Apr 18.
Forkhead box P2 (FOXP2) is a highly conserved transcription factor that has been implicated in human speech and language disorders and plays important roles in the plasticity of the developing brain. The pattern of nucleotide polymorphisms in FOXP2 in modern populations suggests that it has been the target of positive (Darwinian) selection during recent human evolution. In our study, we searched for evidence of selection that might have followed FOXP2 adaptations in modern humans. We examined whether or not putative FOXP2 targets identified by chromatin-immunoprecipitation genomic screening show evidence of positive selection. We developed an algorithm that, for any given gene list, systematically generates matched lists of control genes from the Ensembl database, collates summary statistics for three frequency-spectrum-based neutrality tests from the low-coverage resequencing data of the 1000 Genomes Project, and determines whether these statistics are significantly different between the given gene targets and the set of controls. Overall, there was strong evidence of selection of FOXP2 targets in Europeans, but not in the Han Chinese, Japanese, or Yoruba populations. Significant outliers included several genes linked to cellular movement, reproduction, development, and immune cell trafficking, and 13 of these constituted a significant network associated with cardiac arteriopathy. Strong signals of selection were observed for CNTNAP2 and RBFOX1, key neurally expressed genes that have been consistently identified as direct FOXP2 targets in multiple studies and that have themselves been associated with neurodevelopmental disorders involving language dysfunction.
叉头框蛋白 P2(FOXP2)是一种高度保守的转录因子,与人类言语和语言障碍有关,并在大脑发育的可塑性中发挥重要作用。现代人群中 FOXP2 的核苷酸多态性模式表明,它是人类近期进化中正向选择(达尔文选择)的目标。在我们的研究中,我们寻找了可能紧随现代人类 FOXP2 适应而来的选择证据。我们检查了通过染色质免疫沉淀基因组筛选确定的假定 FOXP2 靶标是否显示出正向选择的证据。我们开发了一种算法,对于任何给定的基因列表,该算法系统地从 Ensembl 数据库中生成匹配的对照基因列表,整理来自 1000 基因组计划低覆盖率重测序数据的三个基于频率谱的中性测试的汇总统计信息,并确定这些统计信息在给定的基因靶标和对照组之间是否存在显著差异。总的来说,FOXP2 靶标在欧洲人群中存在强烈的选择证据,但在汉族、日本人和约鲁巴人群中则没有。显著的异常值包括与细胞运动、生殖、发育和免疫细胞迁移相关的几个基因,其中 13 个基因构成了与心脏动脉病变相关的显著网络。选择的强烈信号观察到 CNTNAP2 和 RBFOX1,这两个关键的神经表达基因在多项研究中一致被确定为 FOXP2 的直接靶标,并且它们本身与涉及语言功能障碍的神经发育障碍有关。