Research Computing Center, University of North Carolina, Chapel Hill, North Carolina, United States of America.
PLoS One. 2013;8(1):e54156. doi: 10.1371/journal.pone.0054156. Epub 2013 Jan 11.
The Toll-like receptors represent a largely evolutionarily conserved pathogen recognition machinery responsible for recognition of bacterial, fungal, protozoan, and viral pathogen associated microbial patterns and initiation of inflammatory response. Structurally the Toll-like receptors are comprised of an extracellular leucine rich repeat domain and a cytoplasmic Toll/Interleukin 1 receptor domain. Recognition takes place in the extracellular domain where as the cytoplasmic domain triggers a complex signal network required to sustain appropriate immune response. Signal transduction is regulated by the recruitment of different intracellular adaptors. The Toll-like receptors can be grouped depending on the usage of the adaptor, MyD88, into MyD88-dependent and MyD88 independent subsets. Herein, we present a unique phylogenetic analysis of domain regions of these receptors and their cognate signaling adaptor molecules. Although previously unclear from the phylogeny of full length receptors, these analyses indicate a separate evolutionary origin for the MyD88-dependent and MyD88-independent signaling pathway and provide evidence of a common ancestor for the vertebrate and invertebrate orthologs of the adaptor molecule MyD88. Together these observations suggest a very ancient origin of the MyD88-dependent pathway Additionally we show that early duplications gave rise to several adaptor molecule families. In some cases there is also strong pattern of parallel duplication between adaptor molecules and their corresponding TLR. Our results further support the hypothesis that phylogeny of specific domains involved in signaling pathway can shed light on key processes that link innate to adaptive immune response.
Toll 样受体是一种广泛进化保守的病原体识别机制,负责识别细菌、真菌、原生动物和病毒病原体相关的微生物模式,并启动炎症反应。在结构上,Toll 样受体由细胞外富含亮氨酸的重复结构域和细胞内 Toll/白细胞介素 1 受体结构域组成。识别发生在细胞外结构域,而细胞质结构域触发复杂的信号网络,以维持适当的免疫反应。信号转导受不同细胞内衔接子的募集调节。根据衔接子 MyD88 的使用情况,Toll 样受体可分为 MyD88 依赖性和 MyD88 非依赖性亚群。在此,我们对这些受体及其同源信号衔接子分子的结构域区域进行了独特的系统发育分析。尽管以前从全长受体的系统发育中不清楚,但这些分析表明,MyD88 依赖性和 MyD88 非依赖性信号通路有单独的进化起源,并为衔接子分子 MyD88 的脊椎动物和无脊椎动物直系同源物提供了共同祖先的证据。这些观察结果共同表明,MyD88 依赖性途径的起源非常古老。此外,我们还表明,早期的复制导致了几个衔接子分子家族的产生。在某些情况下,衔接子分子与其相应的 TLR 之间也存在强烈的平行复制模式。我们的研究结果进一步支持了这样的假设,即信号通路中特定结构域的系统发育可以揭示将先天免疫与适应性免疫反应联系起来的关键过程。