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Gene expression variability across cells and species shapes innate immunity

机译:跨细胞和物种形状的基因表达变异性与生俱来的免疫力

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摘要

As the first line of defence against pathogens, cells mount an innate immune response, which varies widely from cell to cell. The response must be potent but carefully controlled to avoid self-damage. How these constraints have shaped the evolution of innate immunity remains poorly understood. Here we characterize the innate immune response's transcriptional divergence between species and variability in expression among cells. Using bulk and single-cell transcriptomics in fibroblasts and mononuclear phagocytes from different species, challenged with immune stimuli, we map the architecture of the innate immune response. Transcriptionally diverging genes, including those that encode cytokines and chemokines, vary across cells and have distinct promoter structures. Conversely, genes that are involved in the regulation of this response, such as those that encode transcription factors and kinases, are conserved between species and display low cell-to-cell variability in expression. We suggest that this expression pattern, which is observed across species and conditions, has evolved as a mechanism for fine-tuned regulation to achieve an effective but balanced response.
机译:作为抵抗病原体的第一道防线,细胞会产生先天的免疫反应,这种免疫反应会因细胞而异。响应必须有效,但要小心控制以避免自我伤害。这些限制如何影响先天免疫的进化仍知之甚少。在这里,我们描述了物种之间固有的免疫反应的转录差异和细胞之间表达的差异。使用来自不同物种的成纤维细胞和单核吞噬细胞中的大量和单细胞转录组学,受到免疫刺激的挑战,我们绘制了先天免疫应答的结构。转录上不同的基因,包括编码细胞因子和趋化因子的基因,在细胞之间变化,并具有不同的启动子结构。相反,参与该反应调节的基因,例如编码转录因子和激酶的基因,在物种之间是保守的,并且在表达中显示出低的细胞间变异性。我们建议这种表达模式,已跨物种和条件观察到,已演变为微调调控的机制,以实现有效但平衡的响应。

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  • 来源
    《Nature》 |2018年第7730期|197-202|共6页
  • 作者单位

    Wellcome Sanger Inst Cambridge England|EMBL European Bioinformat Inst Cambridge England;

    Wellcome Sanger Inst Cambridge England;

    Wellcome Sanger Inst Cambridge England|Univ Minho Ctr Biol Engn Braga Portugal;

    Univ Turin Dept Life Sci & Syst Biol Turin Italy|IIGM Turin Italy;

    Univ Turin Dept Life Sci & Syst Biol Turin Italy|Univ Turin Mol Biotechnol Ctr Turin Italy;

    Wellcome Sanger Inst Cambridge England|Wellcome Sanger Inst Open Targets Cambridge England;

    EMBL European Bioinformat Inst Cambridge England;

    Newcastle Univ Inst Cellular Med Newcastle Upon Tyne Tyne & Wear England;

    Biomed Primate Res Ctr Anim Sci Dept Div Pathol & Microbiol Rijswijk Netherlands;

    Natl Infect Serv Publ Hlth England Res Dept Porton Down England;

    Newcastle Univ Inst Cellular Med Newcastle Upon Tyne Tyne & Wear England|Newcastle Hosp NHS Fdn Trust Dept Dermatol Newcastle Upon Tyne Tyne & Wear England|Newcastle Hosp NHS Fdn Trust NIHR Newcastle Biomed Res Ctr Newcastle Upon Tyne Tyne & Wear England;

    Max Planck Inst Dynam & Self Org Gottingen Germany|Univ Washington Dept Phys Seattle WA 98195 USA;

    Univ Cologne Inst Biol Phys Cologne Germany;

    Wellcome Sanger Inst Cambridge England|EMBL European Bioinformat Inst Cambridge England|Univ Cambridge Cavendish Lab Theory Condensed Matter Grp Cambridge England;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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