This study aims to comprehensively study the effects of Ca^(2+) on the SA-induced resistance Botrytis cinerea in tomato through proteomics analysis.A proteomic approach was used to uncover the inducible proteins of to...This study aims to comprehensively study the effects of Ca^(2+) on the SA-induced resistance Botrytis cinerea in tomato through proteomics analysis.A proteomic approach was used to uncover the inducible proteins of tomato in the susceptible tomato cultivars ‘L402' against Botrytis cinerea after salicylic acid(SA) and a combination treatment of CaCl_2 and SA.The results showed that the use of combination treatment of CaCl_2 and SA significantly enhanced tomato resistance against Botrytis cinerea.In total,46 differentially expressed protein spots from 2-DE gel maps were detected,of which 41 were identified by mass spectrometry.All the identified proteins were categorized into eight groups according to their putative functions:defense response(14.00%),antioxidative protein(9.75%),photosynthesis(24.39%),molecular chaperone(4.88%),energy(17.01%),metabolism(21.95%),protein synthesis(4.88%) and signal transduction(0.2%).Of the proteins in the eight function groups,the effect of stress/defense and reactive oxygen species on Ca^(2+) -regulated SA-induced resistance may be the most important one in induced resistance by RT-PCR.The expression level of pathogenesis-related proteins(PRs) and chitinase was upregulated by a combination treatment of CaCl_2 and SA.The characterization of these proteins greatly helped to reveal the induced proteins involved in the regulation of Ca^(2+) on SA-induced resistance to Botrytis cinerea.In the combination treatment of CaCl_2 and SA,the defense response and antioxidative protein were clearly upregulated much more than SA alone or the control treatment by the method of proteomics and RT-PCR.The present findings suggest that susceptible tomato cultivars treated by the combination treatment of CaCl_2 and SA might possess a more sensitive SA signaling system or effective pathway than SA treatment alone.In addition,results indicated that SA could coordinate other cellular activities linked with photosynthesis and metabolism to facilitate defense response and recovery,indicating that the self-defense capability of tomato was improved by the combination treatment of CaCl_2 and SA.展开更多
The advent of clustered regularly interspaced short palindromic repeat(CRISPR) has had a profound impact on plant biology, and crop improvement. In this review, we summarize the state-of-the-art development of CRISPR ...The advent of clustered regularly interspaced short palindromic repeat(CRISPR) has had a profound impact on plant biology, and crop improvement. In this review, we summarize the state-of-the-art development of CRISPR technologies and their applications in plants, from the initial introduction of random small indel(insertion or deletion) mutations at target genomic loci to precision editing such as base editing, prime editing and gene targeting. We describe advances in the use of class 2, types II, V, and VI systems for gene disruption as well as for precise sequence alterations, gene transcription, and epigenome control.展开更多
基金supported by the National Natural Science Foundation of China under grants No.313084the National Higher-education Institution General Research and Development Project under Grant No.DC201502070403the Doctor Research Fund of Dalian Minzu University
文摘This study aims to comprehensively study the effects of Ca^(2+) on the SA-induced resistance Botrytis cinerea in tomato through proteomics analysis.A proteomic approach was used to uncover the inducible proteins of tomato in the susceptible tomato cultivars ‘L402' against Botrytis cinerea after salicylic acid(SA) and a combination treatment of CaCl_2 and SA.The results showed that the use of combination treatment of CaCl_2 and SA significantly enhanced tomato resistance against Botrytis cinerea.In total,46 differentially expressed protein spots from 2-DE gel maps were detected,of which 41 were identified by mass spectrometry.All the identified proteins were categorized into eight groups according to their putative functions:defense response(14.00%),antioxidative protein(9.75%),photosynthesis(24.39%),molecular chaperone(4.88%),energy(17.01%),metabolism(21.95%),protein synthesis(4.88%) and signal transduction(0.2%).Of the proteins in the eight function groups,the effect of stress/defense and reactive oxygen species on Ca^(2+) -regulated SA-induced resistance may be the most important one in induced resistance by RT-PCR.The expression level of pathogenesis-related proteins(PRs) and chitinase was upregulated by a combination treatment of CaCl_2 and SA.The characterization of these proteins greatly helped to reveal the induced proteins involved in the regulation of Ca^(2+) on SA-induced resistance to Botrytis cinerea.In the combination treatment of CaCl_2 and SA,the defense response and antioxidative protein were clearly upregulated much more than SA alone or the control treatment by the method of proteomics and RT-PCR.The present findings suggest that susceptible tomato cultivars treated by the combination treatment of CaCl_2 and SA might possess a more sensitive SA signaling system or effective pathway than SA treatment alone.In addition,results indicated that SA could coordinate other cellular activities linked with photosynthesis and metabolism to facilitate defense response and recovery,indicating that the self-defense capability of tomato was improved by the combination treatment of CaCl_2 and SA.
基金supported by the Australian Research Council(LP190100509)National Natural Science Foundation of China (No. 31671273 and No. 32070396)+1 种基金Key Research and Development Plan of Shaanxi Province (No. 2020ZDLNY01-03)the Chinese Academy of Sciences。
文摘The advent of clustered regularly interspaced short palindromic repeat(CRISPR) has had a profound impact on plant biology, and crop improvement. In this review, we summarize the state-of-the-art development of CRISPR technologies and their applications in plants, from the initial introduction of random small indel(insertion or deletion) mutations at target genomic loci to precision editing such as base editing, prime editing and gene targeting. We describe advances in the use of class 2, types II, V, and VI systems for gene disruption as well as for precise sequence alterations, gene transcription, and epigenome control.