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引用次数: 0
摘要
众所周知,免疫反应不断受到包括病原体在内的不同因素的进化压力。虽然不同的选择机制会对免疫反应的大小产生影响,但定量研究免疫反应所受不同选择压力模式的研究却很有限。我利用进化模型(奥恩斯坦-乌伦贝克模型)确定了来自 18 种哺乳动物和一种脊椎动物的成纤维细胞在病毒配体、聚 I: C 或干扰素 alpha 细胞因子刺激下的抗病毒免疫反应的不同选择模式。我发现稳定选择是免疫反应的主要选择形式。在至少 15 个物种的 59 个基因中,发现有 50 个基因处于稳定选择之下。此外,还发现这些与抗病毒有关的保守反应基因之间的进化变异各不相同。例如,发现 ADAR 的进化方差较小,而 TRIM14 的反应则呈现相反的趋势,这表明不同的进化压力对反应的大小产生了影响。在灵长类动物(如猿猴和旧世界猴)的特定下级中,也发现了先天免疫效应因子的定向选择。
Characterizing patterns of selection pressure on mammalian antiviral immune response
Immune response is known to be under constant evolutionary pressure from different factors including pathogens. Although different selection regimes are expected to act on the magnitude of immune response, there are limited studies that have investigated the different patterns of selection pressures on the immune response quantitatively. I employed evolutionary models (Ornstein-Uhlenbeck models) to identify different patterns of selection on the antiviral immune response of fibroblasts derived from 18 mammalian species and one vertebrate stimulated by viral ligand, poly I: C, or Interferon alpha cytokine. I found stabilizing selection to be the dominant form of selection on the immune response. Out of 59 genes that were found to be responding in at least 15 species, 50 genes were found to be under stabilizing selection. Moreover, the evolutionary variance was found to differ among these conservatively responding genes implicated in fighting viruses. For instance, ADAR was found to have low evolutionary variance while TRIM14 response showed the opposite trend suggesting different evolutionary pressures acting on the magnitude of response. Directional selection was also detected in specific infra-orders of primates such as apes and old-world monkeys in response of innate immune effectors.
期刊介绍:
Journal of Mammalian Evolution is a multidisciplinary forum devoted to studies on the comparative morphology, molecular biology, paleobiology, genetics, developmental and reproductive biology, biogeography, systematics, ethology and ecology, and population dynamics of mammals and the ways that these diverse data can be analyzed for the reconstruction of mammalian evolution. The journal publishes high-quality peer-reviewed original articles and reviews derived from both laboratory and field studies. The journal serves as an international forum to facilitate communication among researchers in the multiple fields that contribute to our understanding of mammalian evolutionary biology.