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{"title":"Structural Insights into WY Domain SLiM-Containing Conserved RxLR Effectors: A Case Study of Five Important <i>Phytophthora</i> Species.","authors":"B C Salasini, J Chepsergon, C I Nxumalo, L N Moleleki","doi":"10.1094/MPMI-11-24-0144-R","DOIUrl":null,"url":null,"abstract":"<p><p>Pathogenicity in <i>Phytophthora</i> species is in part underpinned by a sophisticated arsenal of RxLR effectors, which function as molecular determinants of host immune manipulation. Among these, conserved RxLR effectors (CREs) represent an evolutionarily conserved subset that is indispensable for virulence. However, the structural basis of their function remains poorly understood. Here, we conducted in silico analysis of CREs across five agriculturally significant <i>Phytophthora</i> species, revealing a conserved subset that integrates WY domains with embedded short linear motifs (SLiMs), a previously recognized architectural feature with functional implications. Notably, our findings indicate that despite the canonical association of SLiMs with intrinsically disordered regions, their incorporation within the structured WY domain preserves domain integrity while potentially expanding the effector's interactome within host cells. To explore the functional relevance of this domain organization, we characterized <i>Phytophthora nicotianae</i> RxLR6 (PpRxLR6), a representative WY-SLiM CRE identified in this study. Using <i>Agrobacterium</i>-mediated transient expression assays, we demonstrate that PpRxLR6 activates key immune defense networks in <i>Nicotiana</i> and <i>Solanum</i> species, suggesting a role in modulating host immune signaling. Structural predictions further reveal that PpRxLR6 harbors its SLiM within a well-ordered WY-like helical core region, suggesting that SLiM-mediated interactions may occur within structured effector domains rather than being confined to intrinsically disordered regions. These findings enhance our understanding of the effector domain architecture of PpRxLR6, illustrating how structured domains in CREs may serve as scaffolds for SLiM-mediated interactions. This structural arrangement may represent an adaptive strategy in <i>Phytophthora</i> evolution, potentially enhancing effector versatility in host interactions and immune modulation. [Formula: see text] Copyright © 2026 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license.</p>","PeriodicalId":19009,"journal":{"name":"Molecular Plant-microbe Interactions","volume":" ","pages":"14-30"},"PeriodicalIF":3.9000,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Plant-microbe Interactions","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1094/MPMI-11-24-0144-R","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/8 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
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Abstract
Pathogenicity in Phytophthora species is in part underpinned by a sophisticated arsenal of RxLR effectors, which function as molecular determinants of host immune manipulation. Among these, conserved RxLR effectors (CREs) represent an evolutionarily conserved subset that is indispensable for virulence. However, the structural basis of their function remains poorly understood. Here, we conducted in silico analysis of CREs across five agriculturally significant Phytophthora species, revealing a conserved subset that integrates WY domains with embedded short linear motifs (SLiMs), a previously recognized architectural feature with functional implications. Notably, our findings indicate that despite the canonical association of SLiMs with intrinsically disordered regions, their incorporation within the structured WY domain preserves domain integrity while potentially expanding the effector's interactome within host cells. To explore the functional relevance of this domain organization, we characterized Phytophthora nicotianae RxLR6 (PpRxLR6), a representative WY-SLiM CRE identified in this study. Using Agrobacterium -mediated transient expression assays, we demonstrate that PpRxLR6 activates key immune defense networks in Nicotiana and Solanum species, suggesting a role in modulating host immune signaling. Structural predictions further reveal that PpRxLR6 harbors its SLiM within a well-ordered WY-like helical core region, suggesting that SLiM-mediated interactions may occur within structured effector domains rather than being confined to intrinsically disordered regions. These findings enhance our understanding of the effector domain architecture of PpRxLR6, illustrating how structured domains in CREs may serve as scaffolds for SLiM-mediated interactions. This structural arrangement may represent an adaptive strategy in Phytophthora evolution, potentially enhancing effector versatility in host interactions and immune modulation. [Formula: see text] Copyright © 2026 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license.
含有保守RxLR效应子的WY - slim结构分析——以五种重要疫霉菌为例
疫霉物种的致病性部分是由复杂的RxLR效应物库支撑的,RxLR效应物作为宿主免疫操作的分子决定因素。其中,保守的RxLR效应子(CREs)代表了一个进化上保守的子集,对毒力是不可或缺的。然而,其功能的结构基础仍然知之甚少。在这里,我们对五种农业上重要的疫霉物种的cre进行了计算机分析,揭示了一个保守的子集,该子集将WY结构域与嵌入的短线性motif (SLiMs)集成在一起,这是一个先前被认为具有功能意义的结构特征。值得注意的是,我们的研究结果表明,尽管slim与内在无序区域有典型的关联,但它们在结构化的WY结构域内的结合保留了结构域的完整性,同时可能扩大了宿主细胞内效应体的相互作用组。为了探索该结构域组织的功能相关性,我们对本研究中鉴定的具有代表性的WY-SLiM CRE——疫霉菌(Phytophthora nicotianae) RxLR6 (PpRxLR6)进行了表征。通过农杆菌介导的瞬时表达实验,我们发现PpRxLR6激活了烟草和茄属植物的关键免疫防御网络,表明其在调节宿主免疫信号中起作用。结构预测进一步揭示,PpRxLR6在有序的wy样螺旋核心区中含有SLiM,这表明SLiM介导的相互作用可能发生在结构化的效应域内,而不是局限于内在无序的区域。这些发现增强了我们对PpRxLR6效应域结构的理解,说明了cre中的结构域如何作为瘦介导相互作用的支架。这种结构安排可能代表了疫霉菌进化中的一种适应性策略,潜在地增强了宿主相互作用和免疫调节中的效应物的多功能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。