The Plant Cell最新文献

筛选
英文 中文
Cryptic Fate Priming and Lineage Stabilization during Arabidopsis Anther Development 拟南芥花药发育过程中的隐命运启动和谱系稳定
The Plant Cell Pub Date : 2026-09-05 DOI: 10.1093/plcell/koag262
Jianzheng Wang,Xueyi Zhou,Wenhui Sun,Yeqiao Liu,Shiting Zhang,Hanji Li,Yuhan Zhao,Xinyi Xie,Zhenze Lei,Hong Ma,Fang Chang
{"title":"Cryptic Fate Priming and Lineage Stabilization during\u0000 Arabidopsis\u0000 Anther Development","authors":"Jianzheng Wang,Xueyi Zhou,Wenhui Sun,Yeqiao Liu,Shiting Zhang,Hanji Li,Yuhan Zhao,Xinyi Xie,Zhenze Lei,Hong Ma,Fang Chang","doi":"10.1093/plcell/koag262","DOIUrl":"https://doi.org/10.1093/plcell/koag262","url":null,"abstract":"Abstract Plant germ cells are specified de novo from somatic tissues, yet how early anther progenitors initiate divergent germline and somatic fates remains unclear. Here, we generated a high-resolution single-cell transcriptomic atlas of Arabidopsis anther development, profiling 66,864 cells from early lineage specification through pollen maturation. We resolved major anther cell types and identified an early L2-derived intermediate population, termed the archesporial-derived state (Ar-d), marked by REM22, ER/ERL1/2, SPL/NZZ, and BAM1. Although classical anatomical studies define archesporial cells, primary sporogenous cells, primary parietal cells, and secondary parietal derivatives based on developmental position and inferred lineage relationships, our analysis showed that these early L2-derived intermediates remain globally similar, forming a shared progenitor-like transcriptional state before lineage stabilization. Trajectory reconstruction, RNA velocity, and module analyses revealed that germline and somatic trajectories first emerge through restricted branch-biased transcriptional programs, which are later amplified into robust lineage-specific identities. Mutant single-cell analyses defined two regulatory steps: SPL/NZZ establishes early branch-associated transcriptional programs within the Ar-d state, whereas EMS1 stabilizes the somatic/tapetal trajectory and restricts inappropriate enrichment of germline-associated states. Lineage-resolved analyses further defined maturation programs in germline, tapetum, middle layer, and endothecium cells, and identified LBD transcription factors required for normal pollen development. Together, our study reveals a cryptic mode of anther fate priming in which shared early L2-derived intermediates progressively transform limited branch-biased transcriptional programs into distinct reproductive and somatic cell identities through SPL-dependent priming and EMS1-dependent somatic/tapetal stabilization.","PeriodicalId":501012,"journal":{"name":"The Plant Cell","volume":"35 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148894510","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Diverse haplotypes at a complex Solanum americanum locus confer resistance to Phytophthora infestans and P. capsici 在一个复杂的美洲茄位点上,不同的单倍型赋予了对疫霉和辣椒疫病的抗性
The Plant Cell Pub Date : 2026-09-05 DOI: 10.1093/plcell/koag264
Robert Heal,Andrea Carolina Olave-Achury,Maria Sindalovskaya,Ruth Norkor Annang,Shuting Sun,He Zhao,Qing Liu,Li Long,Hari Sharan Karki,Jodie Taylor,Aleksandra Wawryk-Khamdavong,Kinga Bachowska,Matthew Smoker,Maheen Alam,Sarah Pottinger,Vatsal Arora,Kee Hoon Sohn,Kamil Witek,Xiao Lin,Jonathan D G Jones
{"title":"Diverse haplotypes at a complex\u0000 Solanum americanum\u0000 locus confer resistance to\u0000 Phytophthora infestans\u0000 and\u0000 P. capsici","authors":"Robert Heal,Andrea Carolina Olave-Achury,Maria Sindalovskaya,Ruth Norkor Annang,Shuting Sun,He Zhao,Qing Liu,Li Long,Hari Sharan Karki,Jodie Taylor,Aleksandra Wawryk-Khamdavong,Kinga Bachowska,Matthew Smoker,Maheen Alam,Sarah Pottinger,Vatsal Arora,Kee Hoon Sohn,Kamil Witek,Xiao Lin,Jonathan D G Jones","doi":"10.1093/plcell/koag264","DOIUrl":"https://doi.org/10.1093/plcell/koag264","url":null,"abstract":"Abstract Plants encounter diverse pathogens and have evolved a two-layered innate immune system to detect pathogen molecules and activate defense mechanisms that restrict infection. Most cloned plant Resistance (R) genes encode NLR immune receptors. NLR genes are often found in clusters of paralogs with sequence and copy number variation; whether these NLR clusters evolve in response to single or multiple pathogens has been unclear. We report here the isolation of a Phytophthora capsici resistance gene, Rpc2, along with a novel P. infestans resistance gene, Rpi-amr5, from two Solanum americanum accessions. These orthologous genes reside in the Rpi-amr1 cluster, which has previously been associated with resistance to P. infestans. By screening RXLR effector libraries of P. infestans and P. capsici, we identified multiple effectors recognised by both NLRs. Our findings highlight the complexity of NLR clusters and evolution driven by interactions with multiple pathogens. This work will underpin efforts to elevate resistance against Phytophthora pathogens and enhances our understanding of NLR evolution.","PeriodicalId":501012,"journal":{"name":"The Plant Cell","volume":"82 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148894509","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
OsKish coordinates with Lunapark and RHD3 to maintain the structural stability of endoplasmic reticulum network in rice OsKish与Lunapark和RHD3协同作用,维持水稻内质网网络的结构稳定性
The Plant Cell Pub Date : 2026-09-03 DOI: 10.1093/plcell/koag260
Pengcheng Zhang, Yihua Wang, Yun Zhu, Yu Zhang, Xiaohang Han, Yu Chen, Jianing Zhang, Bingke Luo, Xiuhao Bao, Hongming Wu, Fan Wang, Ao Zhang, Cailin Lei, Xin Wang, Zhijun Cheng, Chao Li, Yuqiang Liu, Haiyang Wang, Yulong Ren, Jianmin Wan
{"title":"OsKish coordinates with Lunapark and RHD3 to maintain the structural stability of endoplasmic reticulum network in rice","authors":"Pengcheng Zhang, Yihua Wang, Yun Zhu, Yu Zhang, Xiaohang Han, Yu Chen, Jianing Zhang, Bingke Luo, Xiuhao Bao, Hongming Wu, Fan Wang, Ao Zhang, Cailin Lei, Xin Wang, Zhijun Cheng, Chao Li, Yuqiang Liu, Haiyang Wang, Yulong Ren, Jianmin Wan","doi":"10.1093/plcell/koag260","DOIUrl":"https://doi.org/10.1093/plcell/koag260","url":null,"abstract":"The endoplasmic reticulum (ER) is the largest intracellular membrane-bound organelle in eukaryotic cells, comprising an interconnected network of tubules and sheets. Lunapark (LNP) functions as an E3 ubiquitin ligase that targets RHD3, a dynamin-like GTPase essential for homotypic fusion of ER tubules, for proteasomal degradation, thereby modulating ER tubule stability. However, the regulatory mechanism governing LNP activity remains largely unknown. Here, we report the characterization of the rice oskish mutant, which exhibits aberrant aggregation of ER tubules and defective ER exit of seed storage proteins. OsKish is an ER-localized small protein that physically interacts with both OsLNPs and RHD3-like (RHD3L) protein. OsKish stabilizes OsLNPs by suppressing their auto-ubiquitination; concomitantly, OsKish attenuates the membrane fusion activity of RHD3L possibly by inhibiting its oligomerization. Altogether, our studies propose an OsKish–OsLNPs–RHD3L framework for fine-tuning homotypic ER tubule fusion in rice, providing mechanistic insights into the maintenance of ER architecture in plants.","PeriodicalId":501012,"journal":{"name":"The Plant Cell","volume":"53 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148877337","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Small Helix-Loop-Helix Protein NsrC is a Regulator of Phycobilisome Biosynthesis 小螺旋-环-螺旋蛋白NsrC是藻胆酶体生物合成的调节因子
The Plant Cell Pub Date : 2026-08-21 DOI: 10.1093/plcell/koag249
Wenzhe Li, Qian Liu, Shoujin Fan, Zhuo Chen, Jian Zhang, Guoyan Zhao
{"title":"The Small Helix-Loop-Helix Protein NsrC is a Regulator of Phycobilisome Biosynthesis","authors":"Wenzhe Li, Qian Liu, Shoujin Fan, Zhuo Chen, Jian Zhang, Guoyan Zhao","doi":"10.1093/plcell/koag249","DOIUrl":"https://doi.org/10.1093/plcell/koag249","url":null,"abstract":"Nitrogen is a key nutrient that influences primary productivity in both aquatic and terrestrial ecosystems. In cyanobacteria, its deficiency affects growth, phycobiliprotein biosynthesis, and leads to degradation of phycobilisomes (PBSs). While the biosynthesis genes of phycobiliprotein are regulated by strong promoters, the molecular mechanisms underlying their regulation in response to nitrogen deficiency remain largely unknown. Using non-diazotrophic cyanobacterium Synechococcus elongatus PCC 7942 as a model system, we identified a novel PBS biosynthesis regulator, a small helix-loop-helix protein, designated the Nitrogen Starvation Regulator of the cpc Operon (NsrC). The nsrC gene was transcriptionally activated by nitrogen starvation. The nsrC knockout delayed cell chlorosis during nitrogen starvation, increased oxygen evolution, and significantly elevated PBS protein content. NsrC directly bound to the promoter region of the cpc operon, inhibiting the expression of PBS structural genes, including cpcA and cpcB. Moreover, there was an interaction between NsrC and PII, a signal transduction protein sensing the carbon/nitrogen balance. The binding of NsrC to PII was modulated by the metabolite 2-oxoglutarate (2-OG), which accumulates under nitrogen starvation conditions. Elevated 2-OG levels promoted PII-NsrC complex dissociation, facilitating NsrC binding to the cpc operon and inhibiting PBS expression. Moreover, NsrC is conserved and widely distributed in cyanobacteria and red algae that retain the PBS light-harvesting apparatus; however, it exhibits structural and functional divergence when compared to those found in diatoms and brown algae. Overall, our results showed that the PII-NsrC axis regulates PBS biosynthesis, offering insights into the adaptive mechanisms of cyanobacteria and red algae under nitrogen starvation.","PeriodicalId":501012,"journal":{"name":"The Plant Cell","volume":"10 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148806411","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Chromatin Homogenization Triggers Burst of CHH Methylation in Soybean 染色质均质化引发大豆CHH甲基化爆发
The Plant Cell Pub Date : 2026-08-19 DOI: 10.1093/plcell/koag250
Lesheng Cao, Tianxu Zhang, Shuang Ma, Lishan Wang, Wanpeng Wang, Peng Zhang, Min Wang, Bowei Chen, Zihui Zhang, Yile Guo, Haowen Chen, Luzia Valentina Modolo, Jiang Wang, Linan Xie, Qingzhu Zhang
{"title":"Chromatin Homogenization Triggers Burst of CHH Methylation in Soybean","authors":"Lesheng Cao, Tianxu Zhang, Shuang Ma, Lishan Wang, Wanpeng Wang, Peng Zhang, Min Wang, Bowei Chen, Zihui Zhang, Yile Guo, Haowen Chen, Luzia Valentina Modolo, Jiang Wang, Linan Xie, Qingzhu Zhang","doi":"10.1093/plcell/koag250","DOIUrl":"https://doi.org/10.1093/plcell/koag250","url":null,"abstract":"Although chromatin states are closely associated with epigenetic modifications, how they influence each other remains to be fully elucidated. In this study, we found that mutation of DECREASED IN DNA METHYLATION 1 (DDM1) in soybean leads to genome-wide chromatin homogenization, characterized by a loosening of heterochromatin and a tightening of euchromatin. This remodeling triggers two distinct molecular pathways: in heterochromatin, increased release of small RNAs activates the non-canonical RdDM pathway; while in euchromatin, transposable elements (TEs) are enriched with H3K9me2 modifications, which in turn activate the CMT2 pathway. Together, these pathways drive a pronounced burst of CHH methylation at the whole genome level. This epigenetic remodeling correlates with massive transcriptional dysregulation, upregulating stress responses and downregulating photosynthesis, linking local H3K9me2 changes on TEs, ultimately leading to severe phenotypes. Our findings reveal a unique, bidirectional pathway for CHH regulation in plants with complex chromatin states remodeling.","PeriodicalId":501012,"journal":{"name":"The Plant Cell","volume":"36 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148768126","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Chorismate and isochorismate turnover reveal hidden dynamics of aromatic metabolism in Arabidopsis leaves choris酸和等choris酸转换揭示了拟南芥叶片芳香代谢的隐藏动力学
The Plant Cell Pub Date : 2026-08-19 DOI: 10.1093/plcell/koag251
Anya E Franks, Scott A Ford, Anya Hu, Christina De Melo, Sonia E Evans, Matthew E Bergman, Michael A Phillips
{"title":"Chorismate and isochorismate turnover reveal hidden dynamics of aromatic metabolism in Arabidopsis leaves","authors":"Anya E Franks, Scott A Ford, Anya Hu, Christina De Melo, Sonia E Evans, Matthew E Bergman, Michael A Phillips","doi":"10.1093/plcell/koag251","DOIUrl":"https://doi.org/10.1093/plcell/koag251","url":null,"abstract":"The shikimate pathway provides precursors for phenolic metabolites in plant primary and secondary metabolism. Carbon flux measurements in intact Arabidopsis leaves using an MS2 isotopologue methodology revealed unexpected dynamics between chorismate and isochorismate pools. 13CO2 labeling kinetics point to chloroplast-derived shikimate as a major bifurcation point, with approximately one third diverted from the chloroplast. In contrast, the small pool of chorismate was mostly chloroplast-localized and turned over rapidly, reaching more than 70% labeling within minutes. Isochorismate, a precursor to salicylic acid (SA) in the Brassicales, was present at 50-fold molar excess over chorismate but labeled more slowly and appeared primarily extra-chloroplastic. Total isochorismate declined by 90% in the Arabidopsis enhanced disease susceptibility mutant, which lacks the isochorismate exporter. Non-aqueous fractionation further supported a primarily chloroplast-localized chorismate pool but extra-plastidic isochorismate. Populus trichocarpa and Nicotiana benthamiana leaves contained chorismate but only trace isochorismate, consistent with use of the benzoyl-CoA route to SA. Carbon commitment calculations indicated that one third of the total chorismate pool in Arabidopsis leaves is diverted to isochorismate. Global leaf calculations based on elemental analysis-isotope ratio mass spectrometry and targeted isotope recovery indicate that only 0.03% of total assimilated carbon (5.27 pmol·mg-1 D.W.·min-1) enters the shikimate pathway in photosynthetic tissue of Arabidopsis thaliana. For comparison ∼0.05% (7.75 pmol·mg-1 D.W.·min-1) enters the 2-C-methyl-D-erythritol 4-phosphate pathway, which provides precursors for photosynthetic pigments and electron carriers. The compartmentalization and turnover dynamics of shikimate, chorismate, and isochorismate suggest continuous demand for aromatic precursors in mesophyll tissue is comparable to demand for MEP-pathway derived pigments.","PeriodicalId":501012,"journal":{"name":"The Plant Cell","volume":"7 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148768130","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
OsWOX13 functions as a heading signal transducer from integrator Ehd1 to florigen for the accurate regulation of rice heading date OsWOX13作为从积分器Ehd1到花原的抽穗信号换能器,对水稻抽穗日期进行精确调控
The Plant Cell Pub Date : 2026-08-17 DOI: 10.1093/plcell/koag246
Ming Yu, Minrui Chen, Xudong Zhu, Xinyue Zhang, Maohong Cai, Liang Zhou, Shirong Zhou, Chen Wang, Chao Li, Yimin Ling, Minxi Wu, Limin Zhang, Dekun Lei, Bingke Luo, Qiyu Yang, Wen Li, Xin Jin, Lizhuo Ma, Yulong Ren, Zhichao Zhao, Jie Wang, Cailin Lei, Zhijun Cheng, Qibing Lin, Xiuping Guo, Xin Wang, Shanshan Zhu, Jianmin Wan
{"title":"OsWOX13 functions as a heading signal transducer from integrator Ehd1 to florigen for the accurate regulation of rice heading date","authors":"Ming Yu, Minrui Chen, Xudong Zhu, Xinyue Zhang, Maohong Cai, Liang Zhou, Shirong Zhou, Chen Wang, Chao Li, Yimin Ling, Minxi Wu, Limin Zhang, Dekun Lei, Bingke Luo, Qiyu Yang, Wen Li, Xin Jin, Lizhuo Ma, Yulong Ren, Zhichao Zhao, Jie Wang, Cailin Lei, Zhijun Cheng, Qibing Lin, Xiuping Guo, Xin Wang, Shanshan Zhu, Jianmin Wan","doi":"10.1093/plcell/koag246","DOIUrl":"https://doi.org/10.1093/plcell/koag246","url":null,"abstract":"Appropriate heading date is an important safeguard for stabilizing rice yield and quality. Heading integrator Ehd1 and florigen Hd3a are crucial for rice heading. However, the mechanism by which Ehd1 transmits heading signals to Hd3a and the accurate regulation of Hd3a expression remains unclear. Here, we found that OsWOX13 functions as a signal transducer from Ehd1 to Hd3a for the accurate regulation of rice heading date. Ehd1 can directly bind to the OsWOX13 promoter, OsWOX13 in turn binds to the Hd3a promoter to activate its expression. OsWOX13 interacts with Hd3a to inhibit OsWOX13-mediated activation of Hd3a expression, that precisely controls Hd3a levels. Meanwhile, late-heading phenotypes were observed in the ehd1, Oswox13, Oswox13 ehd1, hd3a, and Oswox13 hd3a, demonstrating that Ehd1, OsWOX13, and Hd3a coordinately regulate rice heading date. Furthermore, OsWOX13 can be divided into two haplotypes, Hap-T and Hap-C. Ehd1 elevated OsWOX13 expression in Hap-T compared with Hap-C. Longjing 31T-C (carrying Hap-C) exhibited later heading dates than Longjing 31 (carrying Hap-T). Rice varieties carrying the Hap-T are predominantly cultivated in high-latitude regions. This study provides genetic resources and a theoretical foundation for improving the regional and climatic adaptability of rice.","PeriodicalId":501012,"journal":{"name":"The Plant Cell","volume":"32 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-08-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148754678","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
LF1 mediates brassinosteroid signaling to regulate leaf angle development in rice LF1介导油菜素内酯信号调控水稻叶片角发育
The Plant Cell Pub Date : 2026-08-14 DOI: 10.1093/plcell/koag247
Jing You, Bingyu Ning, Yi Zhang, Jichao Zhang, Wenwen Xiao, Yan Chen, Jianyan Mu, Zhongyi Zheng, Yunyan Mo, Yuxin Wang, Xianchun Sang, Yinghua Ling, Guanghua He, Ting Zhang
{"title":"LF1 mediates brassinosteroid signaling to regulate leaf angle development in rice","authors":"Jing You, Bingyu Ning, Yi Zhang, Jichao Zhang, Wenwen Xiao, Yan Chen, Jianyan Mu, Zhongyi Zheng, Yunyan Mo, Yuxin Wang, Xianchun Sang, Yinghua Ling, Guanghua He, Ting Zhang","doi":"10.1093/plcell/koag247","DOIUrl":"https://doi.org/10.1093/plcell/koag247","url":null,"abstract":"Leaf angle is a key determinant of plant architecture and grain yield in rice, yet the complex genetic regulatory network remains unclear. Here, we reveal that the HD-ZIP III transcription factor LF1 mediates BR signaling to modulate leaf angle. A miRNA165/166-resistant, gain-of-function lf1 mutant displays an enlarged leaf angle driven by elongated adaxial parenchymal cells and diminished abaxial sclerenchyma. At the transcriptional level, the BR-activated transcription factor OsBZR1 directly induces LF1, which in turn upregulates OsOFP8, forming an OsBZR1-LF1-OsOFP8 hierarchical transcriptional cascade that mediates BR signaling to regulate leaf angle development. At the post-translational level, LF1 protein stability is fine-tuned by reciprocal post-translational modifications, wherein OsMAPK6-mediated phosphorylation at Thr148 promotes LF1 accumulation and transcriptional activity, directly counteracting its ubiquitination and degradation by the APC/CTAD1 complex. Genetic analyses demonstrate that LF1, OsMAPK6, and TAD1 function in a common pathway to regulate leaf angle development. Overall, our study establishes LF1 as a central hub coupling transcriptional and post-translational mechanisms to modulate BR-mediated leaf angle, providing targets for plant architecture improvement.","PeriodicalId":501012,"journal":{"name":"The Plant Cell","volume":"11 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-08-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148754360","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
N-Glycosylation Mediates Smut Effector Adaptation Toward a Host Pectin Methylesterase Inhibitor n -糖基化介导黑穗病效应物对宿主果胶甲基化酯酶抑制剂的适应
The Plant Cell Pub Date : 2026-08-07 DOI: 10.1093/plcell/koag234
Chibbhi Bhaskar, Ee Yang Teoh, Minh-Quang Chau, Chao-Hsuan Yeh, Wei-Lun Tsai, Ooi-Kock Teh, Lay-Sun Ma
{"title":"N-Glycosylation Mediates Smut Effector Adaptation Toward a Host Pectin Methylesterase Inhibitor","authors":"Chibbhi Bhaskar, Ee Yang Teoh, Minh-Quang Chau, Chao-Hsuan Yeh, Wei-Lun Tsai, Ooi-Kock Teh, Lay-Sun Ma","doi":"10.1093/plcell/koag234","DOIUrl":"https://doi.org/10.1093/plcell/koag234","url":null,"abstract":"The demethylation status of pectin, a major plant cell wall polysaccharide, is regulated by pectin methylesterases (PMEs) and their endogenous inhibitors (PMEIs). While PME-mediated removal of methyl groups increases pectin susceptibility to enzymatic degradation and facilitates wall remodeling, this process is suppressed by PMEIs to strengthen the wall, preventing pathogen invasion. How biotrophic pathogens overcome this inhibitory defense remains unclear. Here, we demonstrate how N-glycosylation serves as a post-translational mechanism that pre-shapes a conserved smut effector, directing its adaptation toward a host-specific PMEI to facilitate colonization. We identify the Ustilago maydis N-glycosylated effector Nge1, which interacts with two host inhibitors, PMEI45 and PMEI46, to suppress their inhibitory function. This release of PME activity leads to highly demethylated pectin in the host cell wall that is prone to degradation, likely driving the cell wall loosening favored by pathogens. Crucially, we show that N-glycosylation of Nge1 is essential for its interaction with PMEI45, whereas the interaction with PMEI46 is glycosylation-independent. Engineering N-glycosylation sites into a naturally non-glycosylated Nge1 ortholog restored its ability to neutralize host PMEIs and functionally complement the U. maydis Δnge1 mutant. Our findings reveal that smut fungi utilize post-translational glycan modifications to fine-tune effector specificity, allowing them to overcome host-adapted PMEIs and manipulate plant cell wall dynamics in an ongoing plant-fungal interplay.","PeriodicalId":501012,"journal":{"name":"The Plant Cell","volume":"3 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148703455","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
DELLA proteins interact with HAC1 and control plant growth via transcriptional regulation of the growth repressor gene ERF2 DELLA蛋白与HAC1相互作用,并通过生长抑制基因ERF2的转录调控来控制植物生长
The Plant Cell Pub Date : 2026-08-07 DOI: 10.1093/plcell/koag235
Hiroki Ando, Akira Nozawa, Hidetaka Kosako, Tatsuya Sawasaki, Yohsuke Takahashi, Jutarou Fukazawa
{"title":"DELLA proteins interact with HAC1 and control plant growth via transcriptional regulation of the growth repressor gene ERF2","authors":"Hiroki Ando, Akira Nozawa, Hidetaka Kosako, Tatsuya Sawasaki, Yohsuke Takahashi, Jutarou Fukazawa","doi":"10.1093/plcell/koag235","DOIUrl":"https://doi.org/10.1093/plcell/koag235","url":null,"abstract":"DELLA proteins are negative regulators of gibberellin (GA) signaling. Under GA-deficient conditions, DELLA accumulates in the nucleus and interacts with numerous transcription factors (TFs) via the GRAS domain. Recent studies have shown that DELLA interacts with TFs via the LHR1 subdomain and histone H2A via the PFYRE subdomain, respectively. It is essential for DELLA-mediated global transcription reprogramming. DELLA exhibits strong transcriptional activity and acts as a co-activator of GAI-ASSOCIATED FACTOR1 (GAF1)/IDD2. The N-terminus of DELLA is necessary for strong transcriptional activity, but the regulatory activities and mechanisms of DELLA remain unclear. Therefore, we screened DELLA-interacting factors using the proximity biotinylation enzyme AirID and identified HISTONE ACETYLTRANSFERASE OF THE CBP FAMILY1 (HAC1). HAC1-mediated acetylation of histone H3 at the GAF1 target chromatin was necessary for transcriptional activation by the GAF1-DELLA complex. Additionally, the HAC1-mediated transcriptional activity of DELLA was involved in regulating plant growth. Moreover, ETHYLENE RESPONSE FACTOR2 (ERF2) was identified as a growth repressor gene regulated by the GAF1-DELLA-HAC1 complex. Here, we showed that DELLA proteins regulate plant growth via HAC1-mediated transcriptional regulation of ERF2.","PeriodicalId":501012,"journal":{"name":"The Plant Cell","volume":"8 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148703435","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
相关产品
×
本文献相关产品
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书