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免疫:该基因编码两种具有特定病原体作用的宿主防御肽。

immunity: the gene encodes two host defence peptides with pathogen-specific roles.

机构信息

Global Health Institute, School of Life Science, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.

Invertebrate Genetics Laboratory, Genetic Strains Research Center, National Institute of Genetics, Mishima, Japan.

出版信息

Proc Biol Sci. 2022 Jun 29;289(1977):20220773. doi: 10.1098/rspb.2022.0773. Epub 2022 Jun 22.

Abstract

Antimicrobial peptides (AMPs) are key to defence against infection in plants and animals. Use of AMP mutations in has now revealed that AMPs can additively or synergistically contribute to defence . However, these studies also revealed high specificity, wherein just one AMP contributes an outsized role in combatting a specific pathogen. Here, we show the locus () is more complex than previously described. In addition to its namesake peptide 'Drosocin', it encodes a second mature peptide from a precursor via furin cleavage. This peptide corresponds to the previously uncharacterized 'Immune-induced Molecule 7'. A polymorphism (Thr52Ala) in the Drosocin precursor protein previously masked the identification of this peptide, which we name 'Buletin'. Using mutations differently affecting Drosocin and Buletin, we show that only Drosocin contributes to gene-mediated defence against . Strikingly, we observed that Buletin, but not Drosocin, contributes to the gene-mediated defence against , including an importance of the Thr52Ala polymorphism for survival. Our study reveals that the gene encodes two prominent host defence peptides with different specificity against distinct pathogens. This finding emphasizes the complexity of the humoral response and demonstrates how natural polymorphisms can affect host susceptibility.

摘要

抗菌肽(AMPs)是动植物抗感染防御的关键。在果蝇中对 AMP 突变的利用现在揭示了 AMP 可以叠加或协同地有助于防御。然而,这些研究也揭示了高度的特异性,即只有一种 AMP 在对抗特定病原体方面发挥巨大作用。在这里,我们表明果蝇的 基因座()比以前描述的更为复杂。除了它的同名肽“Drosocin”之外,它还通过 furin 切割从前体编码第二种成熟肽。这种肽对应于以前未被表征的“免疫诱导分子 7”。Drosocin 前体蛋白中的一个多态性(Thr52Ala)以前掩盖了这种肽的鉴定,我们将其命名为“Buletin”。使用不同地影响 Drosocin 和 Buletin 的突变,我们表明只有 Drosocin 有助于 基因介导的对 的防御。引人注目的是,我们观察到 Buletin,但不是 Drosocin,有助于 基因介导的对 的防御,包括 Thr52Ala 多态性对生存的重要性。我们的研究揭示了 基因编码两种具有不同特异性的主要宿主防御肽,针对不同的病原体。这一发现强调了 体液反应的复杂性,并表明了自然多态性如何影响宿主易感性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c838/9233930/574a6f6aee93/rspb20220773f01.jpg

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