NLR免疫受体网络的激活与调控。

Jiorgos Kourelis, Hiroaki Adachi
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引用次数: 13

摘要

植物具有多种类型的免疫受体,可以识别不同的病原体分子并激活先天免疫系统。胞内免疫受体家族的核苷酸结合域富含亮氨酸的重复-含蛋白(NLRs)感知易位的病原体效应蛋白并执行强大的免疫反应,包括程序性细胞死亡。许多植物nlr具有感知病原体效应物(传感器nlr)或执行免疫信号(辅助nlr)的功能。亚功能化的NLR形成一个网络型受体系统,称为NLR网络。在这篇综述中,我们重点介绍了NLR网络的概念,讨论了它们是如何形成、激活和调节的。植物中NLR网络主要有两种类型:激活的抗病性1/N需求基因1网络和细胞死亡NLR需求网络。在这两个网络中,多个辅助nlr作为传感器nlr和细胞表面定位免疫受体的信号中枢。此外,这些网络在转录和转录后水平受到调节,并由其他宿主蛋白调节,以确保适当的网络激活和防止自身免疫。植物病原体反过来聚集抑制NLR网络,从而促进感染和疾病。在网络水平上了解NLR免疫系统可以通过突出免疫受体的适当遗传组合来为未来的育种计划提供信息,同时避免有害的自身免疫和病原体的抑制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Activation and Regulation of NLR Immune Receptor Networks.

Plants have many types of immune receptors that recognize diverse pathogen molecules and activate the innate immune system. The intracellular immune receptor family of nucleotide-binding domain leucine-rich repeat-containing proteins (NLRs) perceives translocated pathogen effector proteins and executes a robust immune response, including programmed cell death. Many plant NLRs have functionally specialized to sense pathogen effectors (sensor NLRs) or to execute immune signaling (helper NLRs). Sub-functionalized NLRs form a network-type receptor system known as the NLR network. In this review, we highlight the concept of NLR networks, discussing how they are formed, activated and regulated. Two main types of NLR networks have been described in plants: the ACTIVATED DISEASE RESISTANCE 1/N REQUIREMENT GENE 1 network and the NLR-REQUIRED FOR CELL DEATH network. In both networks, multiple helper NLRs function as signaling hubs for sensor NLRs and cell-surface-localized immune receptors. Additionally, the networks are regulated at the transcriptional and posttranscriptional levels, and are also modulated by other host proteins to ensure proper network activation and prevent autoimmunity. Plant pathogens in turn have converged on suppressing NLR networks, thereby facilitating infection and disease. Understanding the NLR immune system at the network level could inform future breeding programs by highlighting the appropriate genetic combinations of immunoreceptors to use while avoiding deleterious autoimmunity and suppression by pathogens.

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