Amaro Tiago M M M, Thilliez Gaëtan J A, Motion Graham B, Huitema Edgar
Division of Plant Sciences, University of DundeeDundee, UK; Dundee Effector ConsortiumDundee, UK.
Division of Plant Sciences, University of DundeeDundee, UK; Dundee Effector ConsortiumDundee, UK; Cell and Molecular Sciences, The James Hutton InstituteInvergowrie, UK.
Front Plant Sci. 2017 Feb 3;8:99. doi: 10.3389/fpls.2017.00099. eCollection 2017.
Plant associated microbes rely on secreted virulence factors (effectors) to modulate host immunity and ensure progressive infection. Amongst the secreted protein repertoires defined and studied in pathogens to date, the CRNs (for CRinkling and Necrosis) have emerged as one of only a few highly conserved protein families, spread across several kingdoms. CRN proteins were first identified in plant pathogenic oomycetes where they were found to be modular factors that are secreted and translocated inside host cells by means of a conserved N-terminal domain. Subsequent localization and functional studies have led to the view that CRN C-termini execute their presumed effector function in the host nucleus, targeting processes required for immunity. These findings have led to great interest in this large protein family and driven the identification of additional CRN-like proteins in other organisms. The identification of CRN proteins and subsequent functional studies have markedly increased the number of candidate CRN protein sequences, expanded the range of phenotypes tentatively associated with function and revealed some of their molecular functions toward virulence. The increased number of characterized CRNs also has presented a set of challenges that may impede significant progress in the future. Here, we summarize our current understanding of the CRNs and re-assess some basic assumptions regarding this protein family. We will discuss the latest findings on CRN biology and highlight exciting new hypotheses that have emanated from the field. Finally, we will discuss new approaches to study CRN functions that would lead to a better understanding of CRN effector biology as well as the processes that lead to host susceptibility and immunity.
与植物相关的微生物依靠分泌的毒力因子(效应蛋白)来调节宿主免疫并确保渐进性感染。在迄今为止在病原体中定义和研究的分泌蛋白库中,CRN(引起皱缩和坏死)已成为仅有的几个高度保守的蛋白家族之一,分布在几个王国中。CRN蛋白最初在植物致病卵菌中被鉴定出来,在那里它们被发现是模块化因子,通过保守的N端结构域分泌并转运到宿主细胞内。随后的定位和功能研究得出这样的观点,即CRN的C端在宿主细胞核中执行其假定的效应子功能,靶向免疫所需的过程。这些发现引起了人们对这个大蛋白家族的极大兴趣,并推动了在其他生物体中鉴定更多类似CRN的蛋白。CRN蛋白的鉴定和随后的功能研究显著增加了候选CRN蛋白序列的数量,扩大了与功能初步相关的表型范围,并揭示了它们对毒力的一些分子功能。已鉴定的CRN数量增加也带来了一系列挑战,可能会阻碍未来的重大进展。在这里,我们总结了我们目前对CRN的理解,并重新评估了关于这个蛋白家族的一些基本假设。我们将讨论CRN生物学的最新发现,并强调该领域提出的令人兴奋的新假设。最后,我们将讨论研究CRN功能的新方法,这将有助于更好地理解CRN效应子生物学以及导致宿主易感性和免疫的过程。