Plant PhysiologyPub Date : 2026-10-06DOI: 10.1093/plphys/kiag664
Laura Rehneke, Rory Osborne, Silke Lehmann, Yingqi Zhang, Jemma Roberts, Stefan Altmann, Eva Köpff, Ruth Eichmann, Pascal Falter-Braun, Weixing Shan, Patrick Schäfer
{"title":"Symbiont effectors modulate plant signaling to increase host stress resilience.","authors":"Laura Rehneke, Rory Osborne, Silke Lehmann, Yingqi Zhang, Jemma Roberts, Stefan Altmann, Eva Köpff, Ruth Eichmann, Pascal Falter-Braun, Weixing Shan, Patrick Schäfer","doi":"10.1093/plphys/kiag664","DOIUrl":"10.1093/plphys/kiag664","url":null,"abstract":"<p><p>Plant-colonizing mutualistic symbionts confer beneficial effects to their hosts, which often includes increased growth as well as biotic and abiotic stress resilience. How these benefits are activated on a molecular level is mostly unknown. Here, we describe effector candidates of the fungal symbiont Serendipita indica (Si), which modulate plant stress signaling pathways. By analyzing the Si effector interactome, we reveal frequent targeting of stress-related host proteins, which are linked to the identified effector signaling functions. Moreover, functional data indicate that Si effectors modulate abiotic stress response of Arabidopsis, as well as resistance to pathogen infection. Analysis of symbiont effectors might not only uncover previously unreported molecular mechanisms that increase plant fitness but might also be used to identify potential genetic traits for crop improvement under changing climates.</p>","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":" ","pages":""},"PeriodicalIF":8.2,"publicationDate":"2026-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13655452/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148912981","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Plant PhysiologyPub Date : 2026-10-06DOI: 10.1093/plphys/kiag670
Antoine Beckers, Olivia Vantroeyen, Chantal Cazevieille, Hélène Adam, Gabriel Krouk, Pascal Gantet, Laurent Laplaze, Soazig Guyomarc'h
{"title":"PUCHI controls MYB94 and MYB96 to form the root cap cuticle of developing lateral roots.","authors":"Antoine Beckers, Olivia Vantroeyen, Chantal Cazevieille, Hélène Adam, Gabriel Krouk, Pascal Gantet, Laurent Laplaze, Soazig Guyomarc'h","doi":"10.1093/plphys/kiag670","DOIUrl":"10.1093/plphys/kiag670","url":null,"abstract":"<p><p>Lateral root organogenesis underlies root branching and plays a key role in plant root system architecture. While the transcriptional and hormonal control of lateral root development has been extensively studied over the past decades, an increasing number of studies highlight the importance of specific metabolic pathways contributing to the lateral root regulatory network. The AP2/ERF transcription factor PUCHI has recently been shown to orchestrate the induction of very-long-chain fatty acid biosynthesis in developing lateral root primordia. In parallel, a root cap cuticle, reminiscent of the very-long-chain fatty acid-rich cuticle covering the emerging primary root, was shown to cover developing lateral root primordia and facilitate their emergence. Here, we demonstrate that PUCHI plays an essential role in lateral root cap cuticle formation. We identified the transcription factors MYB94 and MYB96 as key intermediates in this PUCHI-dependent, cuticle regulatory network. Similar to PUCHI, MYB94 and MYB96 induce the expression of a set of very-long-chain fatty acid- and cutin-related genes in lateral root primordia. The loss of function of either PUCHI or that of MYB94 and MYB96 compromises lateral root cuticle deposition, delays lateral root emergence, and alters the expression pattern of lateral root meristematic genes. These results shed light on a PUCHI- and MYB94 and MYB96-dependent regulatory network controlling the lateral root cap cuticle formation and influencing lateral root primordium development and emergence.</p>","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":"202 2","pages":""},"PeriodicalIF":8.2,"publicationDate":"2026-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13655458/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149170332","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"The small GTP-binding protein GhARAC3 is involved in cotton resistance to\u0000 Verticillium dahliae\u0000 by regulating lignin metabolism","authors":"Yajie Wu,Jinglong Zhou,Feng Wei,Lihong Zhao,Yalin Zhang,Zili Feng,Yong Song,Yanjun Li,Xinyu Zhang,Feng Liu,Jie Sun,Jun Zhao,Tao Zhang,Qianhao Zhu,Heqin Zhu,Hongjie Feng","doi":"10.1093/plphys/kiag734","DOIUrl":"https://doi.org/10.1093/plphys/kiag734","url":null,"abstract":"Abstract Plant Rho/ROP GTPases act as essential molecular switches in disease resistance. However, how their protein stability is regulated and integrated with lignin metabolism remains poorly understood. Here, we demonstrate that the cotton small GTPase GhARAC3 serves as a positive regulator of resistance against the vascular pathogen Verticillium dahliae (V. dahliae). Genetic analyses reveal that overexpression of GhARAC3 enhances defense responses in cotton and Arabidopsis, whereas its silencing significantly compromises plant immunity. Under normal physiological conditions, the E3 ubiquitin ligase GhKEG acts as a key regulator that targets GhARAC3 for proteasomal degradation by ubiquitinating multiple lysine residues. Notably, the lysine 161 (K161) residue within the conserved G5 motif is identified as an in vivo ubiquitination site. Mutation of this residue (K161R) impairs GTPase activity and compromises disease resistance, without altering its subcellular localization at the plasma membrane and nucleus. Pathogen infection attenuates this ubiquitination to promote the stabilization of GhARAC3. Genetic epistasis analysis indicates that GhARAC3 requires GhLAC14, a transmembrane laccase, to confer effective immunity.Rather than altering GhLAC14 protein stability, GhARAC3 physically interacts with and stimulates the enzymatic activity of the laccase. Additionally, GhARAC3 promotes reactive oxygen species (ROS) production. This dual activation of laccase activity and the ROS burst drives the rapid deposition of guaiacyl lignin to fortify the plant cell wall. Furthermore, transcriptomic profiling reveals that GhARAC3 broadly upregulates downstream defense-related pathways. Collectively, our findings uncover a regulatory module linking ubiquitin-mediated GTPase turnover to laccase activation, providing a mechanistic framework for improving cotton disease resistance.","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":"7 1","pages":""},"PeriodicalIF":7.4,"publicationDate":"2026-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149090425","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}