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IsDge10 is a hypercompact TnpB nuclease that confers efficient genome editing in rice. IsDge10 是一种超小型 TnpB 核酸酶,它能在水稻中实现高效的基因组编辑。
IF 9.4 1区 生物学
Plant Communications Pub Date : 2024-08-21 DOI: 10.1016/j.xplc.2024.101068
Rui Zhang, Xu Tang, Yao He, Yangcun Li, Wei Wang, Yawei Wang, Danning Wang, Xuelian Zheng, Yiping Qi, Yong Zhang
{"title":"IsDge10 is a hypercompact TnpB nuclease that confers efficient genome editing in rice.","authors":"Rui Zhang, Xu Tang, Yao He, Yangcun Li, Wei Wang, Yawei Wang, Danning Wang, Xuelian Zheng, Yiping Qi, Yong Zhang","doi":"10.1016/j.xplc.2024.101068","DOIUrl":"10.1016/j.xplc.2024.101068","url":null,"abstract":"","PeriodicalId":52373,"journal":{"name":"Plant Communications","volume":null,"pages":null},"PeriodicalIF":9.4,"publicationDate":"2024-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142019552","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}
引用次数: 0
The abscisic acid-responsive transcriptional regulatory module CsERF110-CsERF53 orchestrates citrus fruit coloration. 脱落酸响应转录调控模块 CsERF110-CsERF53 协调柑橘果实着色。
IF 9.4 1区 生物学
Plant Communications Pub Date : 2024-08-20 DOI: 10.1016/j.xplc.2024.101065
Quan Sun, Zhengchen He, Di Feng, Ranran Wei, Yingzi Zhang, Junli Ye, Lijun Chai, Juan Xu, Yunjiang Cheng, Qiang Xu, Xiuxin Deng
{"title":"The abscisic acid-responsive transcriptional regulatory module CsERF110-CsERF53 orchestrates citrus fruit coloration.","authors":"Quan Sun, Zhengchen He, Di Feng, Ranran Wei, Yingzi Zhang, Junli Ye, Lijun Chai, Juan Xu, Yunjiang Cheng, Qiang Xu, Xiuxin Deng","doi":"10.1016/j.xplc.2024.101065","DOIUrl":"10.1016/j.xplc.2024.101065","url":null,"abstract":"<p><p>Carotenoid biosynthesis is closely associated with abscisic acid (ABA) during the ripening process of non-climacteric fruits, but the regulatory mechanism that links ABA signaling to carotenoid metabolism remains largely unclear. Here, we identified two master regulators of ABA-mediated citrus fruit coloration, CsERF110 and CsERF53, which activate the expression of carotenoid metabolism genes (CsGGPPS, CsPSY, CsPDS, CsCRTISO, CsLCYB2, CsLCYE, CsHYD, CsZEP, and CsNCED2) to facilitate carotenoid accumulation. Further investigations showed that CsERF110 not only activates the expression of CsERF53 by binding to its promoter but also interacts with CsERF53 to form the transcriptional regulatory module CsERF110-CsERF53. We also discovered a positive feedback regulatory loop between the ABA signal and carotenoid metabolism regulated by the transcriptional regulatory module CsERF110-CsERF53. Our results reveal that the CsERF110-CsERF53 module responds to ABA signaling, thereby orchestrating citrus fruit coloration. Considering the importance of carotenoid content for citrus and many other carotenoid-rich crops, the revelation of molecular mechanisms that underlie ABA-mediated carotenoid biosynthesis in plants will facilitate the development of transgenic/gene-editing approaches, further contributing to improving the quality of citrus and other carotenoid-rich crops.</p>","PeriodicalId":52373,"journal":{"name":"Plant Communications","volume":null,"pages":null},"PeriodicalIF":9.4,"publicationDate":"2024-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142009891","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}
引用次数: 0
Direct RNA sequencing in plants: Practical applications and future perspectives. 植物中的直接 RNA 测序:实际应用与未来展望。
IF 9.4 1区 生物学
Plant Communications Pub Date : 2024-08-18 DOI: 10.1016/j.xplc.2024.101064
Xi-Tong Zhu, Pablo Sanz-Jimenez, Xiao-Tong Ning, Muhammad Tahir Ul Qamar, Ling-Ling Chen
{"title":"Direct RNA sequencing in plants: Practical applications and future perspectives.","authors":"Xi-Tong Zhu, Pablo Sanz-Jimenez, Xiao-Tong Ning, Muhammad Tahir Ul Qamar, Ling-Ling Chen","doi":"10.1016/j.xplc.2024.101064","DOIUrl":"10.1016/j.xplc.2024.101064","url":null,"abstract":"<p><p>The transcriptome serves as a bridge that links genomic variation to phenotypic diversity. A vast number of studies using next-generation RNA sequencing (RNA-seq) over the last 2 decades have emphasized the essential roles of the plant transcriptome in response to developmental and environmental conditions, providing numerous insights into the dynamic changes, evolutionary traces, and elaborate regulation of the plant transcriptome. With substantial improvement in accuracy and throughput, direct RNA sequencing (DRS) has emerged as a new and powerful sequencing platform for precise detection of native and full-length transcripts, overcoming many limitations such as read length and PCR bias that are inherent to short-read RNA-seq. Here, we review recent advances in dissecting the complexity and diversity of plant transcriptomes using DRS as the main technological approach, covering many aspects of RNA metabolism, including novel isoforms, poly(A) tails, and RNA modification, and we propose a comprehensive workflow for processing of plant DRS data. Many challenges to the application of DRS in plants, such as the need for machine learning tools tailored to plant transcriptomes, remain to be overcome, and together we outline future biological questions that can be addressed by DRS, such as allele-specific RNA modification. This technology provides convenient support on which the connection of distinct RNA features is tightly built, sustainably refining our understanding of the biological functions of the plant transcriptome.</p>","PeriodicalId":52373,"journal":{"name":"Plant Communications","volume":null,"pages":null},"PeriodicalIF":9.4,"publicationDate":"2024-08-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142001308","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}
引用次数: 0
A fast and genotype-independent in planta Agrobacterium-mediated transformation method for soybean. 大豆植物体内农杆菌介导的快速、不依赖基因型的转化方法。
IF 9.4 1区 生物学
Plant Communications Pub Date : 2024-08-13 DOI: 10.1016/j.xplc.2024.101063
Heng Zhong, Changbao Li, Wenjin Yu, Hua-Ping Zhou, Tara Lieber, Xiujuan Su, Wenling Wang, Eric Bumann, Rafaela Miranda Lunny Castro, Yaping Jiang, Wening Gu, Qingli Liu, Brenden Barco, Chengjin Zhang, Liang Shi, Qiudeng Que
{"title":"A fast and genotype-independent in planta Agrobacterium-mediated transformation method for soybean.","authors":"Heng Zhong, Changbao Li, Wenjin Yu, Hua-Ping Zhou, Tara Lieber, Xiujuan Su, Wenling Wang, Eric Bumann, Rafaela Miranda Lunny Castro, Yaping Jiang, Wening Gu, Qingli Liu, Brenden Barco, Chengjin Zhang, Liang Shi, Qiudeng Que","doi":"10.1016/j.xplc.2024.101063","DOIUrl":"10.1016/j.xplc.2024.101063","url":null,"abstract":"<p><p>Efficient genotype-independent transformation and genome editing are highly desirable for plant biotechnology research and product development efforts. We have developed a novel approach to enable fast, high-throughput, and genotype-flexible Agrobacterium-mediated transformation using the important crop soybean as a test system. This new method is called GiFT (genotype-independent fast transformation) and involves only a few simple steps. The method uses germinated seeds as explants, and DNA delivery is achieved through Agrobacterium infection of wounded explants as in conventional in vitro-based methods. Following infection, the wounded explants are incubated in liquid medium with a sublethal level of selection and then transplanted directly into soil. The transplanted seedlings are then selected with herbicide spray for 3 weeks. The time required from initiation to fully established healthy T0 transgenic events is about 35 days. The GiFT method requires minimal in vitro manipulation or use of tissue culture media. Because the regeneration occurs in planta, the GiFT method is highly flexible with respect to genotype, which we demonstrate via successful transformation of elite germplasms from diverse genetic backgrounds. We also show that the soybean GiFT method can be applied to both conventional binary vectors and CRISPR-Cas12a vectors for genome editing applications. Analyses of T1 progeny demonstrate that the events have a high inheritance rate and can be used for genome engineering applications. By minimizing the need for tissue culture, the novel approach described here significantly improves operational efficiency while greatly reducing personnel and supply costs. It is the first industry-scale transformation method to utilize in planta selection in a major field crop.</p>","PeriodicalId":52373,"journal":{"name":"Plant Communications","volume":null,"pages":null},"PeriodicalIF":9.4,"publicationDate":"2024-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141977168","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}
引用次数: 0
Single-cell transcriptome atlases of soybean root and mature nodule reveal new regulatory programs that control the nodulation process. 大豆根和成熟结节的单细胞转录组图谱揭示了控制结瘤过程的新调控程序。
IF 9.4 1区 生物学
Plant Communications Pub Date : 2024-08-12 Epub Date: 2024-06-06 DOI: 10.1016/j.xplc.2024.100984
Sergio Alan Cervantes-Pérez, Prince Zogli, Sahand Amini, Sandra Thibivilliers, Sutton Tennant, Md Sabbir Hossain, Hengping Xu, Ian Meyer, Akash Nooka, Pengchong Ma, Qiuming Yao, Michael J Naldrett, Andrew Farmer, Olivier Martin, Samik Bhattacharya, Jasper Kläver, Marc Libault
{"title":"Single-cell transcriptome atlases of soybean root and mature nodule reveal new regulatory programs that control the nodulation process.","authors":"Sergio Alan Cervantes-Pérez, Prince Zogli, Sahand Amini, Sandra Thibivilliers, Sutton Tennant, Md Sabbir Hossain, Hengping Xu, Ian Meyer, Akash Nooka, Pengchong Ma, Qiuming Yao, Michael J Naldrett, Andrew Farmer, Olivier Martin, Samik Bhattacharya, Jasper Kläver, Marc Libault","doi":"10.1016/j.xplc.2024.100984","DOIUrl":"10.1016/j.xplc.2024.100984","url":null,"abstract":"<p><p>The soybean root system is complex. In addition to being composed of various cell types, the soybean root system includes the primary root, the lateral roots, and the nodule, an organ in which mutualistic symbiosis with N-fixing rhizobia occurs. A mature soybean root nodule is characterized by a central infection zone where atmospheric nitrogen is fixed and assimilated by the symbiont, resulting from the close cooperation between the plant cell and the bacteria. To date, the transcriptome of individual cells isolated from developing soybean nodules has been established, but the transcriptomic signatures of cells from the mature soybean nodule have not yet been characterized. Using single-nucleus RNA-seq and Molecular Cartography technologies, we precisely characterized the transcriptomic signature of soybean root and mature nodule cell types and revealed the co-existence of different sub-populations of B. diazoefficiens-infected cells in the mature soybean nodule, including those actively involved in nitrogen fixation and those engaged in senescence. Mining of the single-cell-resolution nodule transcriptome atlas and the associated gene co-expression network confirmed the role of known nodulation-related genes and identified new genes that control the nodulation process. For instance, we functionally characterized the role of GmFWL3, a plasma membrane microdomain-associated protein that controls rhizobial infection. Our study reveals the unique cellular complexity of the mature soybean nodule and helps redefine the concept of cell types when considering the infection zone of the soybean nodule.</p>","PeriodicalId":52373,"journal":{"name":"Plant Communications","volume":null,"pages":null},"PeriodicalIF":9.4,"publicationDate":"2024-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11369782/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141285385","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}
引用次数: 0
Pull the fuzes: Processing protein precursors to generate apoplastic danger signals for triggering plant immunity. 拉动引信处理蛋白质前体,生成引发植物免疫的细胞外危险信号。
IF 9.4 1区 生物学
Plant Communications Pub Date : 2024-08-12 Epub Date: 2024-04-30 DOI: 10.1016/j.xplc.2024.100931
Daniele Del Corpo, Daniele Coculo, Marco Greco, Giulia De Lorenzo, Vincenzo Lionetti
{"title":"Pull the fuzes: Processing protein precursors to generate apoplastic danger signals for triggering plant immunity.","authors":"Daniele Del Corpo, Daniele Coculo, Marco Greco, Giulia De Lorenzo, Vincenzo Lionetti","doi":"10.1016/j.xplc.2024.100931","DOIUrl":"10.1016/j.xplc.2024.100931","url":null,"abstract":"<p><p>The apoplast is one of the first cellular compartments outside the plasma membrane encountered by phytopathogenic microbes in the early stages of plant tissue invasion. Plants have developed sophisticated surveillance mechanisms to sense danger events at the cell surface and promptly activate immunity. However, a fine tuning of the activation of immune pathways is necessary to mount a robust and effective defense response. Several endogenous proteins and enzymes are synthesized as inactive precursors, and their post-translational processing has emerged as a critical mechanism for triggering alarms in the apoplast. In this review, we focus on the precursors of phytocytokines, cell wall remodeling enzymes, and proteases. The physiological events that convert inactive precursors into immunomodulatory active peptides or enzymes are described. This review also explores the functional synergies among phytocytokines, cell wall damage-associated molecular patterns, and remodeling, highlighting their roles in boosting extracellular immunity and reinforcing defenses against pests.</p>","PeriodicalId":52373,"journal":{"name":"Plant Communications","volume":null,"pages":null},"PeriodicalIF":9.4,"publicationDate":"2024-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11371470/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140858985","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}
引用次数: 0
Diverse nucleotide substitutions in rice base editing mediated by novel TadA variants. 由新型 TadA 变体介导的水稻碱基编辑中的多种核苷酸置换。
IF 9.4 1区 生物学
Plant Communications Pub Date : 2024-08-12 Epub Date: 2024-05-08 DOI: 10.1016/j.xplc.2024.100926
Man Yu, Yongjie Kuang, Chenyang Wang, Xuemei Wu, Shaofang Li, Dawei Zhang, Wenxian Sun, Xueping Zhou, Bin Ren, Huanbin Zhou
{"title":"Diverse nucleotide substitutions in rice base editing mediated by novel TadA variants.","authors":"Man Yu, Yongjie Kuang, Chenyang Wang, Xuemei Wu, Shaofang Li, Dawei Zhang, Wenxian Sun, Xueping Zhou, Bin Ren, Huanbin Zhou","doi":"10.1016/j.xplc.2024.100926","DOIUrl":"10.1016/j.xplc.2024.100926","url":null,"abstract":"<p><p>CRISPR-mediated base editors have been widely used to correct defective alleles and create novel alleles by artificial evolution for the rapid genetic improvement of crops. The editing capabilities of base editors strictly rely on the performance of various nucleotide modification enzymes. Compared with the well-developed adenine base editors (ABEs), cytosine base editors (CBEs) and dual base editors suffer from unstable editing efficiency and patterns at different genomic loci in rice, significantly limiting their application. Here, we comprehensively examined the base editing activities of multiple evolved TadA8e variants in rice. We found that both TadA-CDd and TadA-E27R/N46L achieved more robust C-to-T editing than previously reported hyperactive hAID∗Δ, and TadA-CDd outperformed TadA-E27R/N46L. A C-to-G base editor (CGBE) engineered with TadA-CDd and OsUNG performed highly efficient C-to-G editing in rice compared with that of TadA-N46P. In addition, a dual base editor constructed with a single protein, TadDE, enabled simultaneous, highly efficient C-to-T and A-to-G editing in rice. Collectively, our results demonstrate that TadA8e derivatives improve both CBEs and dual base editors in rice, providing a powerful way to induce diverse nucleotide substitutions for plant genome editing.</p>","PeriodicalId":52373,"journal":{"name":"Plant Communications","volume":null,"pages":null},"PeriodicalIF":9.4,"publicationDate":"2024-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11369719/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140900063","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}
引用次数: 0
A single-cell transcriptome atlas reveals the trajectory of early cell fate transition during callus induction in Arabidopsis. 单细胞转录组图谱揭示了拟南芥胼胝体诱导过程中早期细胞命运转变的轨迹。
IF 9.4 1区 生物学
Plant Communications Pub Date : 2024-08-12 Epub Date: 2024-05-07 DOI: 10.1016/j.xplc.2024.100941
Ruilian Yin, Ruiying Chen, Keke Xia, Xun Xu
{"title":"A single-cell transcriptome atlas reveals the trajectory of early cell fate transition during callus induction in Arabidopsis.","authors":"Ruilian Yin, Ruiying Chen, Keke Xia, Xun Xu","doi":"10.1016/j.xplc.2024.100941","DOIUrl":"10.1016/j.xplc.2024.100941","url":null,"abstract":"<p><p>The acquisition of pluripotent callus from somatic cells plays an important role in plant development studies and crop genetic improvement. This developmental process incorporates a series of cell fate transitions and reprogramming. However, our understanding of cell heterogeneity and mechanisms of cell fate transition during callus induction remains quite limited. Here, we report a time-series single-cell transcriptome experiment on Arabidopsis root explants that were induced in callus induction medium for 0, 1, and 4 days, and the construction of a detailed single-cell transcriptional atlas of the callus induction process. We identify the cell types responsible for initiating the early callus: lateral root primordium-initiating (LRPI)-like cells and quiescent center (QC)-like cells. LRPI-like cells are derived from xylem pole pericycle cells and are similar to lateral root primordia. We delineate the developmental trajectory of the dedifferentiation of LRPI-like cells into QC-like cells. QC-like cells are undifferentiated pluripotent acquired cells that appear in the early stages of callus formation and play a critical role in later callus development and organ regeneration. We also identify the transcription factors that regulate QC-like cells and the gene expression signatures that are related to cell fate decisions. Overall, our cell-lineage transcriptome atlas for callus induction provides a distinct perspective on cell fate transitions during callus formation, significantly improving our understanding of callus formation.</p>","PeriodicalId":52373,"journal":{"name":"Plant Communications","volume":null,"pages":null},"PeriodicalIF":9.4,"publicationDate":"2024-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11369778/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140892819","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}
引用次数: 0
Clathrin light chains negatively regulate plant immunity by hijacking the autophagy pathway. Clathrin Light Chains通过劫持自噬途径对植物免疫进行负面调节。
IF 9.4 1区 生物学
Plant Communications Pub Date : 2024-08-12 Epub Date: 2024-04-30 DOI: 10.1016/j.xplc.2024.100937
Hu-Jiao Lan, Jie Ran, Wen-Xu Wang, Lei Zhang, Ni-Ni Wu, Ya-Ting Zhao, Min-Jun Huang, Min Ni, Fen Liu, Ninghui Cheng, Paul A Nakata, Jianwei Pan, Steven A Whitham, Barbara J Baker, Jian-Zhong Liu
{"title":"Clathrin light chains negatively regulate plant immunity by hijacking the autophagy pathway.","authors":"Hu-Jiao Lan, Jie Ran, Wen-Xu Wang, Lei Zhang, Ni-Ni Wu, Ya-Ting Zhao, Min-Jun Huang, Min Ni, Fen Liu, Ninghui Cheng, Paul A Nakata, Jianwei Pan, Steven A Whitham, Barbara J Baker, Jian-Zhong Liu","doi":"10.1016/j.xplc.2024.100937","DOIUrl":"10.1016/j.xplc.2024.100937","url":null,"abstract":"<p><p>The crosstalk between clathrin-mediated endocytosis (CME) and the autophagy pathway has been reported in mammals; however, the interconnection of CME with autophagy has not been established in plants. Here, we report that the Arabidopsis CLATHRIN LIGHT CHAIN (CLC) subunit 2 and 3 double mutant, clc2-1 clc3-1, phenocopies Arabidopsis AUTOPHAGY-RELATED GENE (ATG) mutants in both autoimmunity and nutrient sensitivity. Accordingly, the autophagy pathway is significantly compromised in the clc2-1 clc3-1 mutant. Interestingly, multiple assays demonstrate that CLC2 directly interacts with ATG8h/ATG8i in a domain-specific manner. As expected, both GFP-ATG8h/GFP-ATG8i and CLC2-GFP are subjected to autophagic degradation, and degradation of GFP-ATG8h is significantly reduced in the clc2-1 clc3-1 mutant. Notably, simultaneous knockout of ATG8h and ATG8i by CRISPR-Cas9 results in enhanced resistance against Golovinomyces cichoracearum, supporting the functional relevance of the CLC2-ATG8h/8i interactions. In conclusion, our results reveal a link between the function of CLCs and the autophagy pathway in Arabidopsis.</p>","PeriodicalId":52373,"journal":{"name":"Plant Communications","volume":null,"pages":null},"PeriodicalIF":9.4,"publicationDate":"2024-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11369776/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140864370","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}
引用次数: 0
Insights into dammarane-type triterpenoid saponin biosynthesis from the telomere-to-telomere genome of Gynostemma pentaphyllum. 从五倍子绞股蓝的端粒到端粒基因组了解达玛烷型三萜类 spaonin 的生物合成。
IF 9.4 1区 生物学
Plant Communications Pub Date : 2024-08-12 Epub Date: 2024-04-30 DOI: 10.1016/j.xplc.2024.100932
Lingling Yun, Chuyi Zhang, Tongtong Liang, Yu Tian, Guoxu Ma, Vincent Courdavault, Sijie Sun, Baiping Ma, Ziqin Li, Rucan Li, Feng Cao, Xiaofeng Shen, Jianhe Wei, Ying Li, Baolin Guo, Chao Sun
{"title":"Insights into dammarane-type triterpenoid saponin biosynthesis from the telomere-to-telomere genome of Gynostemma pentaphyllum.","authors":"Lingling Yun, Chuyi Zhang, Tongtong Liang, Yu Tian, Guoxu Ma, Vincent Courdavault, Sijie Sun, Baiping Ma, Ziqin Li, Rucan Li, Feng Cao, Xiaofeng Shen, Jianhe Wei, Ying Li, Baolin Guo, Chao Sun","doi":"10.1016/j.xplc.2024.100932","DOIUrl":"10.1016/j.xplc.2024.100932","url":null,"abstract":"","PeriodicalId":52373,"journal":{"name":"Plant Communications","volume":null,"pages":null},"PeriodicalIF":9.4,"publicationDate":"2024-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11369773/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140853524","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}
引用次数: 0
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