{"title":"CbuBIM1 Antagonizes CbuMYB27 to Regulate Tension Wood Formation in Catalpa bungei.","authors":"Dian Wang, Shaofeng Li, Shumin Wang, Jichun Li, Junhang Fu, Fei Xia, Nan Lu, Wenjun Ma, Peng Wang, Gongke Zhou, Junhui Wang, Xianfeng Tang","doi":"10.1111/pce.70551","DOIUrl":null,"url":null,"abstract":"<p><p>Catalpa bungei is a valuable timber species famous for its high-quality wood properties, which are greatly compromised by tension wood (TW) formation. However, the molecular mechanisms underlying TW remain unclear. In this study, we identified that CbuMYB27 was specifically upregulated during TW formation in C. bungei. CbuMYB27 exhibits the highest expression level in the stem and its encoded protein possesses transcriptional activation activity. Overexpression of CbuMYB27 in hybrid poplar (84K) resulted in increased cambium layers and xylem width. Further analysis revealed that CbuMYB27 negatively regulates lignin biosynthesis. Molecular analysis indicated that CbuMYB27 positively regulates cambial activity and negatively regulates lignin biosynthesis by directly activating cambium-related genes and suppressing lignin-biosynthetic genes, respectively. Protein interaction assays indicated that CbuMYB27 physically interacts with a bHLH transcription factor, CbuBIM1. Although CbuBIM1 cannot directly regulate the target genes of CbuMYB27, it antagonizes CbuMYB27-mediated transcriptional regulation of these downstream genes. Moreover, CbuBIM1 attenuates the promoting effect of CbuMYB27 in TW formation caused by bending stress. In summary, our findings identify a functionally antagonistic module of CbuMYB27- CbuBIM1, which is involved in TW formation by modulating cambium activity and lignin biosynthesis in C. bungei and thus provides a potential target for the improvement of wood quality in C. bungei.</p>","PeriodicalId":222,"journal":{"name":"Plant, Cell & Environment","volume":" ","pages":"5547-5562"},"PeriodicalIF":6.9000,"publicationDate":"2026-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13353648/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant, Cell & Environment","FirstCategoryId":"2","ListUrlMain":"https://doi.org/10.1111/pce.70551","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/4/22 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Catalpa bungei is a valuable timber species famous for its high-quality wood properties, which are greatly compromised by tension wood (TW) formation. However, the molecular mechanisms underlying TW remain unclear. In this study, we identified that CbuMYB27 was specifically upregulated during TW formation in C. bungei. CbuMYB27 exhibits the highest expression level in the stem and its encoded protein possesses transcriptional activation activity. Overexpression of CbuMYB27 in hybrid poplar (84K) resulted in increased cambium layers and xylem width. Further analysis revealed that CbuMYB27 negatively regulates lignin biosynthesis. Molecular analysis indicated that CbuMYB27 positively regulates cambial activity and negatively regulates lignin biosynthesis by directly activating cambium-related genes and suppressing lignin-biosynthetic genes, respectively. Protein interaction assays indicated that CbuMYB27 physically interacts with a bHLH transcription factor, CbuBIM1. Although CbuBIM1 cannot directly regulate the target genes of CbuMYB27, it antagonizes CbuMYB27-mediated transcriptional regulation of these downstream genes. Moreover, CbuBIM1 attenuates the promoting effect of CbuMYB27 in TW formation caused by bending stress. In summary, our findings identify a functionally antagonistic module of CbuMYB27- CbuBIM1, which is involved in TW formation by modulating cambium activity and lignin biosynthesis in C. bungei and thus provides a potential target for the improvement of wood quality in C. bungei.
期刊介绍:
Plant, Cell & Environment is a premier plant science journal, offering valuable insights into plant responses to their environment. Committed to publishing high-quality theoretical and experimental research, the journal covers a broad spectrum of factors, spanning from molecular to community levels. Researchers exploring various aspects of plant biology, physiology, and ecology contribute to the journal's comprehensive understanding of plant-environment interactions.