The transcriptional cascade and regulatory loop play crucial roles in regulating plant-specialized metabolite biosynthesis.Capsaicinoids are unique to the genus Capsicum and confer a pungent flavor to its fruits.Howev...The transcriptional cascade and regulatory loop play crucial roles in regulating plant-specialized metabolite biosynthesis.Capsaicinoids are unique to the genus Capsicum and confer a pungent flavor to its fruits.However,the transcriptional regulation of capsaicinoid biosynthesis remains largely unknown.In this study,two AP2/ERF transcription factors(TFs),CaERF102 and CaERF111,were characterized for their role in the capsaicinoid biosynthesis process.Expression analysis of two ERFs and capsaicinoid biosynthetic genes(CBGs)suggested that they were associated with capsaicinoid biosynthesis.Both ERFs encode nuclear-localized proteins and function as transcriptional activators through their C-terminal activation motifs.The two ERF TFs participated in capsaicinoid biosynthesis by directly activating the promoters of key CBGs,and this activation was significantly enhanced when CaMYC2 was co-expressed.Moreover,CaERF102 and CaERF111 were found to interact with CaMYC2.This study helps elucidate the AP2/ERF TF regulatory network that governs capsaicinoid biosynthesis in Capsicum species.展开更多
Pepper(Capsicum annuum)is one of the most important horticultural crops worldwide,which makes the development of an effective protoplast system for transient gene expression highly significant.Typically,plant protopla...Pepper(Capsicum annuum)is one of the most important horticultural crops worldwide,which makes the development of an effective protoplast system for transient gene expression highly significant.Typically,plant protoplasts are initially isolated through enzymatic digestion and then used for transient transformations mediated by polyethylene glycol(PEG).However,PEG-mediated protoplast transformation suffers from low and inconsistent efficiency,is influenced by various factors,and requires greater operator expertise.Here,we present a simple and efficient protoplast system for transient gene expression in C.annuum and Nicotiana benthamiana,without PEG-mediated transfection.This procedure involved using the first and second fully expanded true leaves of pepper and N.benthamiana plants at the six-leaf stage for Agrobacterium infiltration,followed by enzymatic digestion for protoplast isolation.The resulting protoplast transfections achieved remarkably high efficiencies,facilitating functional analyses such as subcellular localization and protein—protein interaction studies(for example,BiFC,Co-IP,and Split-LUC assays).Thus,we have demonstrated a simplified and highly efficient transient expression system for protoplasts and potential wide-ranging applications in C.annuum and N.benthamiana while bypassing PEG-mediated transfection.展开更多
Industrial activities have caused widespread arsenic(As)contamination in soil and medicinal crops across south-ern Asia.This study constructed interplanting systems combing medicinal crops with Pteris vittata L.,aimin...Industrial activities have caused widespread arsenic(As)contamination in soil and medicinal crops across south-ern Asia.This study constructed interplanting systems combing medicinal crops with Pteris vittata L.,aiming to mitigate the risk of As exposure in medicinal crops,while simultaneously achieving ecological remediation of contaminated soil.The results revealed that interplanting with P.vittata significantly enhanced the yield of Gynos-temma pentaphyllum by 31.90%(P<0.05)compared with monoculture systems.Under monoculture conditions,the As concentration in G.pentaphyllum leaves reached 2.34 mg/kg,exceeding the national food safety standard(GB2762–2017,2 mg/kg).However,interplanting with P.vittata effectively reduced the As concentration in G.pentaphyllum leaves to 1.82 mg/kg.Furthermore,the interplanting of P.vittata with Rhus chinensis significantly inhibited As translocation from belowground to aboveground tissues in R.chinensis.Compared to monoculture,the stem biomass of P.vittata was significantly increased by 57.50%and 70.32%when interplanted with G.pentaphyllum and Cassia obtusifolia L.(P<0.05).So the As enrichment of P.vittata was enhanced in interplanting systems,which is beneficial for the As removal from contaminated soil.The study demonstrated that interplant-ing primarily regulates plant As uptake through modifications of rhizosphere physicochemical properties and As bioavailability,especially for water-soluble As that is easily absorbed by plants.In conclusion,the interplant-ing models integrating medicinal crops and P.vittata can achieve the goal of“remediating while producing”in As-contaminated soil.展开更多
基金funded by the National Natural Science Foundation of China(Grant Nos.32202502,U21A20230,32070331,32102380 and 32072580)National Key Research and Development Program(Grant No.2018YFD1000800)+3 种基金the Key-Area Research and Development Program of Guangdong Province(Grant No.2022B0202080001)the Special Fund for Seed Industry of Guangdong Province Rural Revitalization Strategy(Grant No.2022-NPY00-024)Tibet Autonomous Region of Lhasa City Science and Technology Project(Grant No.LSKJ202310)the Science and Technology Project of Bijie City(Grant No.BKK2022-3)。
文摘The transcriptional cascade and regulatory loop play crucial roles in regulating plant-specialized metabolite biosynthesis.Capsaicinoids are unique to the genus Capsicum and confer a pungent flavor to its fruits.However,the transcriptional regulation of capsaicinoid biosynthesis remains largely unknown.In this study,two AP2/ERF transcription factors(TFs),CaERF102 and CaERF111,were characterized for their role in the capsaicinoid biosynthesis process.Expression analysis of two ERFs and capsaicinoid biosynthetic genes(CBGs)suggested that they were associated with capsaicinoid biosynthesis.Both ERFs encode nuclear-localized proteins and function as transcriptional activators through their C-terminal activation motifs.The two ERF TFs participated in capsaicinoid biosynthesis by directly activating the promoters of key CBGs,and this activation was significantly enhanced when CaMYC2 was co-expressed.Moreover,CaERF102 and CaERF111 were found to interact with CaMYC2.This study helps elucidate the AP2/ERF TF regulatory network that governs capsaicinoid biosynthesis in Capsicum species.
基金supported by the National Natural Science Foundation of China(Grant Nos.32472536 and 32302526)the Natural Science Foundation of Anhui Province,China(Grant No.2208085MC64)+2 种基金the Outstanding Innovative Research Team for Molecular Enzymology and Detection in Anhui Provincial Universities(Grant No.2022AH010012)the University Synergy Innovation Program of Anhui Province(Grant No.GXXT-2022-067)the University Natural Science Research Program of Anhui Provincial Education Department(Grant No.KJ2021A0118).
文摘Pepper(Capsicum annuum)is one of the most important horticultural crops worldwide,which makes the development of an effective protoplast system for transient gene expression highly significant.Typically,plant protoplasts are initially isolated through enzymatic digestion and then used for transient transformations mediated by polyethylene glycol(PEG).However,PEG-mediated protoplast transformation suffers from low and inconsistent efficiency,is influenced by various factors,and requires greater operator expertise.Here,we present a simple and efficient protoplast system for transient gene expression in C.annuum and Nicotiana benthamiana,without PEG-mediated transfection.This procedure involved using the first and second fully expanded true leaves of pepper and N.benthamiana plants at the six-leaf stage for Agrobacterium infiltration,followed by enzymatic digestion for protoplast isolation.The resulting protoplast transfections achieved remarkably high efficiencies,facilitating functional analyses such as subcellular localization and protein—protein interaction studies(for example,BiFC,Co-IP,and Split-LUC assays).Thus,we have demonstrated a simplified and highly efficient transient expression system for protoplasts and potential wide-ranging applications in C.annuum and N.benthamiana while bypassing PEG-mediated transfection.
基金supported by the National Key Research and Development Program of China(No.2020YFC1807805)the Science and Technology Planning Project of Guangzhou,Guangdong Province,China(No.202206010176).
文摘Industrial activities have caused widespread arsenic(As)contamination in soil and medicinal crops across south-ern Asia.This study constructed interplanting systems combing medicinal crops with Pteris vittata L.,aiming to mitigate the risk of As exposure in medicinal crops,while simultaneously achieving ecological remediation of contaminated soil.The results revealed that interplanting with P.vittata significantly enhanced the yield of Gynos-temma pentaphyllum by 31.90%(P<0.05)compared with monoculture systems.Under monoculture conditions,the As concentration in G.pentaphyllum leaves reached 2.34 mg/kg,exceeding the national food safety standard(GB2762–2017,2 mg/kg).However,interplanting with P.vittata effectively reduced the As concentration in G.pentaphyllum leaves to 1.82 mg/kg.Furthermore,the interplanting of P.vittata with Rhus chinensis significantly inhibited As translocation from belowground to aboveground tissues in R.chinensis.Compared to monoculture,the stem biomass of P.vittata was significantly increased by 57.50%and 70.32%when interplanted with G.pentaphyllum and Cassia obtusifolia L.(P<0.05).So the As enrichment of P.vittata was enhanced in interplanting systems,which is beneficial for the As removal from contaminated soil.The study demonstrated that interplant-ing primarily regulates plant As uptake through modifications of rhizosphere physicochemical properties and As bioavailability,especially for water-soluble As that is easily absorbed by plants.In conclusion,the interplant-ing models integrating medicinal crops and P.vittata can achieve the goal of“remediating while producing”in As-contaminated soil.
