Sungjun Choung,Gisuk Lee,Moonyoung Kang,Kyungsun Park,Eunae Park,Sunghee Lee,Junyong Song,Jay K Goldberg,Ian T Baldwin,Youngsung Joo,Sang-Gyu Kim
{"title":"MYC2和MYC3协调髓木质化,以保护烟草茎免受茎蛀象鼻虫的侵害。","authors":"Sungjun Choung,Gisuk Lee,Moonyoung Kang,Kyungsun Park,Eunae Park,Sunghee Lee,Junyong Song,Jay K Goldberg,Ian T Baldwin,Youngsung Joo,Sang-Gyu Kim","doi":"10.1111/nph.70325","DOIUrl":null,"url":null,"abstract":"Lignin is a key structural polymer that also serves as a potent defense against biotic stress. Herbivore-induced, jasmonate-dependent pith lignification in Nicotiana attenuata plays a crucial role in defense against the stem-borer Trichobaris mucorea. However, the regulatory mechanisms underlying herbivore-induced lignification remain largely unknown. We demonstrate that NaMYC2 and NaMYC3 orchestrate pith-specific lignification in response to T. mucorea attack. RNA-seq analysis reveals that monolignol biosynthetic genes and polymerization-associated genes fail to be induced in Namyc2/3 double mutants upon T. mucorea attack. Among NaMYC2/3-dependent genes in the attacked pith, we identify NaTHT1, responsible for synthesizing the noncanonical monolignol N-FT. Using Natht1 mutants, we further show that N-FT plays a key role in stem defense. Additionally, we identify NaNEC1a and NaNEC1c, NaMYC2/3-dependent superoxide dismutases in the pith. Nanec1a/1c double mutants exhibit reduced lignification and enhanced larval performance, supporting a direct link between superoxide metabolism and induced lignification. Our findings reveal a NaMYC2/3-mediated regulatory network in the pith that integrates monolignol biosynthesis, lignin polymerization, and noncanonical monolignol biosynthesis, thereby enhancing stem defense against T. mucorea.","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"52 1","pages":""},"PeriodicalIF":8.1000,"publicationDate":"2025-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"MYC2 and MYC3 orchestrate pith lignification to defend Nicotiana attenuata stems against a stem-boring weevil.\",\"authors\":\"Sungjun Choung,Gisuk Lee,Moonyoung Kang,Kyungsun Park,Eunae Park,Sunghee Lee,Junyong Song,Jay K Goldberg,Ian T Baldwin,Youngsung Joo,Sang-Gyu Kim\",\"doi\":\"10.1111/nph.70325\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Lignin is a key structural polymer that also serves as a potent defense against biotic stress. Herbivore-induced, jasmonate-dependent pith lignification in Nicotiana attenuata plays a crucial role in defense against the stem-borer Trichobaris mucorea. However, the regulatory mechanisms underlying herbivore-induced lignification remain largely unknown. We demonstrate that NaMYC2 and NaMYC3 orchestrate pith-specific lignification in response to T. mucorea attack. RNA-seq analysis reveals that monolignol biosynthetic genes and polymerization-associated genes fail to be induced in Namyc2/3 double mutants upon T. mucorea attack. Among NaMYC2/3-dependent genes in the attacked pith, we identify NaTHT1, responsible for synthesizing the noncanonical monolignol N-FT. Using Natht1 mutants, we further show that N-FT plays a key role in stem defense. Additionally, we identify NaNEC1a and NaNEC1c, NaMYC2/3-dependent superoxide dismutases in the pith. Nanec1a/1c double mutants exhibit reduced lignification and enhanced larval performance, supporting a direct link between superoxide metabolism and induced lignification. Our findings reveal a NaMYC2/3-mediated regulatory network in the pith that integrates monolignol biosynthesis, lignin polymerization, and noncanonical monolignol biosynthesis, thereby enhancing stem defense against T. mucorea.\",\"PeriodicalId\":214,\"journal\":{\"name\":\"New Phytologist\",\"volume\":\"52 1\",\"pages\":\"\"},\"PeriodicalIF\":8.1000,\"publicationDate\":\"2025-06-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"New Phytologist\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1111/nph.70325\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Phytologist","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/nph.70325","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
MYC2 and MYC3 orchestrate pith lignification to defend Nicotiana attenuata stems against a stem-boring weevil.
Lignin is a key structural polymer that also serves as a potent defense against biotic stress. Herbivore-induced, jasmonate-dependent pith lignification in Nicotiana attenuata plays a crucial role in defense against the stem-borer Trichobaris mucorea. However, the regulatory mechanisms underlying herbivore-induced lignification remain largely unknown. We demonstrate that NaMYC2 and NaMYC3 orchestrate pith-specific lignification in response to T. mucorea attack. RNA-seq analysis reveals that monolignol biosynthetic genes and polymerization-associated genes fail to be induced in Namyc2/3 double mutants upon T. mucorea attack. Among NaMYC2/3-dependent genes in the attacked pith, we identify NaTHT1, responsible for synthesizing the noncanonical monolignol N-FT. Using Natht1 mutants, we further show that N-FT plays a key role in stem defense. Additionally, we identify NaNEC1a and NaNEC1c, NaMYC2/3-dependent superoxide dismutases in the pith. Nanec1a/1c double mutants exhibit reduced lignification and enhanced larval performance, supporting a direct link between superoxide metabolism and induced lignification. Our findings reveal a NaMYC2/3-mediated regulatory network in the pith that integrates monolignol biosynthesis, lignin polymerization, and noncanonical monolignol biosynthesis, thereby enhancing stem defense against T. mucorea.
期刊介绍:
New Phytologist is an international electronic journal published 24 times a year. It is owned by the New Phytologist Foundation, a non-profit-making charitable organization dedicated to promoting plant science. The journal publishes excellent, novel, rigorous, and timely research and scholarship in plant science and its applications. The articles cover topics in five sections: Physiology & Development, Environment, Interaction, Evolution, and Transformative Plant Biotechnology. These sections encompass intracellular processes, global environmental change, and encourage cross-disciplinary approaches. The journal recognizes the use of techniques from molecular and cell biology, functional genomics, modeling, and system-based approaches in plant science. Abstracting and Indexing Information for New Phytologist includes Academic Search, AgBiotech News & Information, Agroforestry Abstracts, Biochemistry & Biophysics Citation Index, Botanical Pesticides, CAB Abstracts®, Environment Index, Global Health, and Plant Breeding Abstracts, and others.