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Autism and Schizophrenia Are Disorders of Evolvability

机译:自闭症和精神分裂症是可进化性障碍

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Autism and schizophrenia are of particular interest because new developments in genomic medicine address three aspects of the conditions that have been difficult, thus far, to resolve: their heterogeneity, from subclinical manifestations to disorders that are gravely disabling; the genetic basis for their high heritability; and the persistence of disorders in light of their high heritability but low reproductive success they convey. The origins of autism and schizophrenia, their persistence and heterogeneity can be understood by integrating information from genomic science, the social brain and the evolution of socialization, intelligence and language. Both conditions are associated with structural changes in the genome, specifically copy number variants. Such systemic mutations contribute to an unstable and mutable genome and have been especially notable during primate > hominid evolution. Along with mechanisms that affect gene expression, they contribute to a genome characterized by variability and evolvability. A dynamic and variable genome is reflected by a high degree of phenotypic variation. This, in turn, is reflected in the diversity of neurodevelopmental disorders, in particular autism and schizophrenia. Evolvability is more than a dispositional concept, it is a trait in its own right. In the special case of hominid evolution, evolvability has been both an independent and a dependent variable. Evolution of the modern human brain seems to have arisen during the cultivation of unstable regions in the genome that were conducive to a high degree of inter-individual and inter-generational variation. The consequence of even small aberrations in evolutionary processes and phenotypic variations is most likely to be manifest in the functions of the social brain: self-referential processing, perspective taking and the dual components of empathy; also language as well as intelligence itself. The trade-off is a dynamic genome that can rearrange itself in untoward ways and may be felt in one or more of the above functions. The occurrence of neurodevelopmental disorders ranging from the learning disabilities and ADD to autism and schizophrenia, are epiphenomenal to a genome that is unstable and mutable. The selective advantage of such a genome is the runaway evolution of positive prosocial and intellective traits. If there is a core to the pathology that emerges in autism and schizophrenia, it is at the genomic level, and is probably related to the unique evolvability of the human genome. Genetic transformation as an agent of evolvability is necessarily associated with untoward consequences. Just as point mutations may have deleterious effects, so do genomic transformations. The neurodevelopmental disorders, therefore, are the consequence of evolvability.
机译:自闭症和精神分裂症特别令人感兴趣,因为基因组医学的新进展解决了迄今为止难以解决的三个方面的疾病:它们的异质性,从亚临床表现到严重致残的疾病;其高遗传力的遗传基础;以及它们传达的遗传力高但生殖成功率低的疾病的持久性。自闭症和精神分裂症的起源,持续性和异质性可以通过整合来自基因组科学,社会大脑以及社会化,智力和语言进化的信息来理解。两种情况都与基因组中的结构变化有关,特别是拷贝数变异。此类系统性突变会导致基因组不稳定和易变,在灵长类动物>人的进化过程中尤为明显。除了影响基因表达的机制外,它们还有助于以变异和进化为特征的基因组。动态和可变的基因组反映在高度的表型变异上。反过来,这又反映在神经发育障碍的多样性上,特别是自闭症和精神分裂症。可进化性不只是一个倾向性的概念,它本身就是一个特征。在原始人进化的特殊情况下,可进化性既是自变量又是因变量。现代人类大脑的进化似乎是在基因组不稳定区域的培育期间出现的,这些区域有利于高度个体间和代际变异。进化过程和表型变异甚至很小的偏差最有可能在社会大脑的功能中得到体现:自我指涉处理,观点采择和共情的双重成分;语言以及智力本身。权衡是一个动态的基因组,它可以以不适当的方式重排自身,并且可以通过一种或多种上述功能感受到。从学习障碍和ADD到自闭症和精神分裂症的神经发育障碍的发生是不稳定和易变的基因组的现象。这种基因组的选择优势是正面亲社会和智力特征的失控进化。如果自闭症和精神分裂症中出现了病理学的核心,那么它就在基因组水平上,并且可能与人类基因组的独特可进化性有关。遗传转化作为可进化性的推动因素必然带来不良后果。正如点突变可能具有有害作用一样,基因组转化也是如此。因此,神经发育障碍是可进化性的结果。

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