Tiantian Fu, Zeqi Wang, Chun Wang, Yuzhang Yang, Ruen Yu, Xiaoqian Yang, Jiahao Liu, Hongkun Ji, Yuanlong Wang, Tianliang Wang, Jieru Li, Yanwei Wang
{"title":"Integrating Transcriptomics and Metabolomics in Poplar to Uncover Crucial Genes and Metabolites in Response to Anoplophora glabripennis Infestation.","authors":"Tiantian Fu, Zeqi Wang, Chun Wang, Yuzhang Yang, Ruen Yu, Xiaoqian Yang, Jiahao Liu, Hongkun Ji, Yuanlong Wang, Tianliang Wang, Jieru Li, Yanwei Wang","doi":"10.1111/ppl.70523","DOIUrl":null,"url":null,"abstract":"<p><p>Anoplophora glabripennis (ALB) is one of the most devastating stem-boring beetles. However, knowledge pertaining to the molecular regulation and key responses of poplars under ALB infestation remains limited. In this investigation, the transcriptomes and metabolomes of two different poplars with different resistances under ALB infestation were jointly analyzed, combined with phytohormone analysis. Two thousand one hundred ninety-five genes, including defense genes such as MYB44, NAC1, and DELLA, were significantly altered in both poplar varieties after ALB infestation. Notably, the elevated levels of JA accumulation, the differential expression of poplar-specific phenolic glycosides, and the significant accumulation of catechins in Populus tomentosa might be the key factors leading to the differential resistance. In addition, the key metabolic enzymes involved in the synthesis of catechins (DFR, LAR, 4CL, CHS, and F3H) were significantly upregulated in P. tomentosa. Intriguingly, the upregulation of numerous resistance genes and the downregulation of a few photosynthesis-related genes in resistant poplars reflect a trade-off strategy between defense and growth. Several transcription factors, including WRKY, were identified in the significant induction of SA and JA signaling pathways in poplars in response to ALB infestation. Taken together, this investigation marked an important step toward elucidating the insect resistance mechanisms in poplar and should provide crucial insights into the development of new insect-resistant poplar varieties.</p>","PeriodicalId":20164,"journal":{"name":"Physiologia plantarum","volume":"177 5","pages":"e70523"},"PeriodicalIF":3.6000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physiologia plantarum","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/ppl.70523","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Anoplophora glabripennis (ALB) is one of the most devastating stem-boring beetles. However, knowledge pertaining to the molecular regulation and key responses of poplars under ALB infestation remains limited. In this investigation, the transcriptomes and metabolomes of two different poplars with different resistances under ALB infestation were jointly analyzed, combined with phytohormone analysis. Two thousand one hundred ninety-five genes, including defense genes such as MYB44, NAC1, and DELLA, were significantly altered in both poplar varieties after ALB infestation. Notably, the elevated levels of JA accumulation, the differential expression of poplar-specific phenolic glycosides, and the significant accumulation of catechins in Populus tomentosa might be the key factors leading to the differential resistance. In addition, the key metabolic enzymes involved in the synthesis of catechins (DFR, LAR, 4CL, CHS, and F3H) were significantly upregulated in P. tomentosa. Intriguingly, the upregulation of numerous resistance genes and the downregulation of a few photosynthesis-related genes in resistant poplars reflect a trade-off strategy between defense and growth. Several transcription factors, including WRKY, were identified in the significant induction of SA and JA signaling pathways in poplars in response to ALB infestation. Taken together, this investigation marked an important step toward elucidating the insect resistance mechanisms in poplar and should provide crucial insights into the development of new insect-resistant poplar varieties.
期刊介绍:
Physiologia Plantarum is an international journal committed to publishing the best full-length original research papers that advance our understanding of primary mechanisms of plant development, growth and productivity as well as plant interactions with the biotic and abiotic environment. All organisational levels of experimental plant biology – from molecular and cell biology, biochemistry and biophysics to ecophysiology and global change biology – fall within the scope of the journal. The content is distributed between 5 main subject areas supervised by Subject Editors specialised in the respective domain: (1) biochemistry and metabolism, (2) ecophysiology, stress and adaptation, (3) uptake, transport and assimilation, (4) development, growth and differentiation, (5) photobiology and photosynthesis.