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{"title":"Insights into <i>Phakopsora pachyrhizi</i> Effector-Effector Interactions.","authors":"Mingsheng Qi, Haiyue Yu, Melissa Bredow, Aline Sartor Chicowski, Letícia Dias Fields, Steven A Whitham","doi":"10.1094/MPMI-08-23-0120-FI","DOIUrl":null,"url":null,"abstract":"<p><p>The multifaceted role of pathogen-encoded effectors in plant-pathogen interactions is complex and not fully understood. Effectors operate within intricate host environments, interacting with host proteins and other effectors to modulate virulence. The complex interplay between effectors raises the concept of metaeffectors, wherein some effectors regulate the activity of others. While previous research has demonstrated the importance of effector repertoires in pathogen virulence, only a limited number of studies have investigated the interactions between these effectors. This study explores the interactions among <i>Phakopsora pachyrhizi</i> effector candidates (<i>Pp</i>ECs). <i>P. pachyrhizi</i> haustorial transcriptome analysis identified a collection of predicted <i>Pp</i>ECs. Among these, <i>Pp</i>EC23 was found to interact with <i>Pp</i>EC48, prompting further exploration into their potential interaction with other effectors. Here, we utilized a yeast two-hybrid screen to explore protein-protein interactions between <i>Pp</i>ECs. A split-luciferase complementation assay also demonstrated that these interactions could occur within soybean cells. Interestingly, <i>Pp</i>EC48 displayed the ability to interact with several small cysteine-rich proteins (SCRPs), suggesting its affinity for this specific class of effectors. We show that these interactions involve a histidine-rich domain within <i>Pp</i>EC48, emphasizing the significance of structural motifs in mediating effector interactions. The unique nature of <i>Pp</i>EC48, showing no sequence matches in other organisms, suggests its relatively recent evolution and potential orphan gene status. Our work reveals insights into the intricate network of interactions among <i>P. pachyrhizi</i> effector-effector interactions. [Formula: see text] Copyright © 2024 The Author(s). This is an open access article distributed under the CC BY 4.0 International license.</p>","PeriodicalId":19009,"journal":{"name":"Molecular Plant-microbe Interactions","volume":" ","pages":"227-231"},"PeriodicalIF":3.2000,"publicationDate":"2024-03-01","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-08-23-0120-FI","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/3/12 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
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Abstract
The multifaceted role of pathogen-encoded effectors in plant-pathogen interactions is complex and not fully understood. Effectors operate within intricate host environments, interacting with host proteins and other effectors to modulate virulence. The complex interplay between effectors raises the concept of metaeffectors, wherein some effectors regulate the activity of others. While previous research has demonstrated the importance of effector repertoires in pathogen virulence, only a limited number of studies have investigated the interactions between these effectors. This study explores the interactions among Phakopsora pachyrhizi effector candidates (Pp ECs). P. pachyrhizi haustorial transcriptome analysis identified a collection of predicted Pp ECs. Among these, Pp EC23 was found to interact with Pp EC48, prompting further exploration into their potential interaction with other effectors. Here, we utilized a yeast two-hybrid screen to explore protein-protein interactions between Pp ECs. A split-luciferase complementation assay also demonstrated that these interactions could occur within soybean cells. Interestingly, Pp EC48 displayed the ability to interact with several small cysteine-rich proteins (SCRPs), suggesting its affinity for this specific class of effectors. We show that these interactions involve a histidine-rich domain within Pp EC48, emphasizing the significance of structural motifs in mediating effector interactions. The unique nature of Pp EC48, showing no sequence matches in other organisms, suggests its relatively recent evolution and potential orphan gene status. Our work reveals insights into the intricate network of interactions among P. pachyrhizi effector-effector interactions. [Formula: see text] Copyright © 2024 The Author(s). This is an open access article distributed under the CC BY 4.0 International license.
深入了解厚叶Phakopsora效应器-效应器的相互作用。
病原体编码的效应子在植物-病原体相互作用中的多方面作用是复杂的,尚未完全理解。效应器在复杂的宿主环境中运作,与宿主蛋白和其他效应器相互作用以调节毒力。效应器之间复杂的相互作用提出了元效应器的概念,其中一些效应器调节其他效应器的活动。虽然先前的研究已经证明了效应子库在病原体毒力中的重要性,但只有有限数量的研究调查了这些效应子之间的相互作用。本研究探讨了厚叶Phakopsora效应候选物(PpECs)之间的相互作用。P.pachyrhizi吸器转录组分析鉴定了一组预测的PpEC。其中,PpEC23被发现与PpEC48相互作用,促使人们进一步探索它们与其他效应物的潜在相互作用。在这里,我们利用酵母双杂交筛选来探索PpEC之间的蛋白质-蛋白质相互作用。分裂萤光素酶互补测定也表明这些相互作用可能发生在大豆细胞内。有趣的是,PpEC48显示出与几种富含半胱氨酸的小蛋白(SCRP)相互作用的能力,这表明它对这类特定效应子具有亲和力。我们发现这些相互作用涉及PpEC48中富含组氨酸的结构域,强调了结构基序在介导效应器相互作用中的重要性。PpEC48的独特性质,在其他生物体中没有显示出序列匹配,这表明它的进化相对较新,并且可能是孤儿基因。我们的工作揭示了对厚脊杆菌效应-效应相互作用之间复杂的相互作用网络的深入了解。
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