Li Ming, Wu Dong-Dong, Yao Yong-Gang, Huo Yong-Xia, Liu Jie-Wei, Su Bing, Chasman Daniel I, Chu Audrey Y, Huang Tao, Qi Lu, Zheng Yan, Luo Xiong-Jian
Key Laboratory of Animal Models and Human Disease Mechanisms of the Chinese Academy of Sciences and Yunnan Province, Kunming Institute of Zoology, Kunming, Yunnan, China; These authors contributed equally to this work. ML and XJL are co-corresponding authors who jointly directed this work.
State Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, Yunnan, China; These authors contributed equally to this work.
Schizophr Bull. 2016 Jan;42(1):178-90. doi: 10.1093/schbul/sbv070. Epub 2015 May 25.
Natural selection has played important roles in optimizing complex human adaptations. However, schizophrenia poses an evolutionary paradox during human evolution, as the illness has strongly negative effects on fitness, but persists with a prevalence of ~0.5% across global populations. Recent studies have identified numerous risk variations in diverse populations, which might be able to explain the stable and high rate of schizophrenia morbidity in different cultures and regions, but the questions about why the risk alleles derived and maintained in human gene pool still remain unsolved. Here, we studied the evolutionary pattern of a schizophrenia risk variant rs13107325 (P < 5.0 × 10(-8) in Europeans) in the SLC39A8 gene. We found the SNP is monomorphic in Asians and Africans with risk (derived) T-allele totally absent, and further evolutionary analyses showed the T-allele has experienced recent positive selection in Europeans. Subsequent exploratory analyses implicated that the colder environment in Europe was the likely selective pressures, ie, when modern humans migrated "out of Africa" and moved to Europe mainland (a colder and cooler continent than Africa), new alleles derived due to positive selection and protected humans from risk of hypertension and also helped them adapt to the cold environment. The hypothesis was supported by our pleiotropic analyses with hypertension and energy intake as well as obesity in Europeans. Our data thus provides an intriguing example to illustrate a possible mechanism for maintaining schizophrenia risk alleles in the human gene pool, and further supported that schizophrenia is likely a product caused by pleiotropic effect during human evolution.
自然选择在优化复杂的人类适应性方面发挥了重要作用。然而,精神分裂症在人类进化过程中构成了一个进化悖论,因为这种疾病对适应性有强烈的负面影响,但在全球人群中持续存在,患病率约为0.5%。最近的研究已经在不同人群中发现了许多风险变异,这可能能够解释不同文化和地区精神分裂症发病率稳定且居高不下的原因,但关于这些风险等位基因为何在人类基因库中产生并得以维持的问题仍然没有得到解决。在这里,我们研究了SLC39A8基因中一个精神分裂症风险变异rs13107325(在欧洲人中P < 5.0 × 10(-8))的进化模式。我们发现该单核苷酸多态性在亚洲人和非洲人中是单态的,风险(衍生)T等位基因完全不存在,进一步的进化分析表明T等位基因在欧洲人中经历了近期的正选择。随后的探索性分析表明,欧洲较寒冷的环境可能是选择压力,也就是说,当现代人类“走出非洲”并迁移到欧洲大陆(一个比非洲更寒冷的大陆)时,由于正选择产生了新的等位基因,这些等位基因保护人类免受高血压风险,也帮助他们适应寒冷环境。我们对欧洲人高血压、能量摄入以及肥胖进行的多效性分析支持了这一假设。因此,我们的数据提供了一个有趣的例子,说明了人类基因库中维持精神分裂症风险等位基因的一种可能机制,并进一步支持精神分裂症可能是人类进化过程中多效性效应导致的产物。