Anne-Sophie Blervacq , Dmitry Galinousky , Clémence Simon , Myriam Moreau , Anne Duputié , Fabien Baldacci-Cresp , Cedric Lion , Christophe Biot , Simon Hawkins , Godfrey Neutelings
{"title":"Tracking ectopic lignification in flax stems following scarification","authors":"Anne-Sophie Blervacq , Dmitry Galinousky , Clémence Simon , Myriam Moreau , Anne Duputié , Fabien Baldacci-Cresp , Cedric Lion , Christophe Biot , Simon Hawkins , Godfrey Neutelings","doi":"10.1016/j.plaphy.2025.109806","DOIUrl":null,"url":null,"abstract":"<div><div>When flax (<em>Linum usitatissimum</em> L.) stems are scarified, major changes occur in the organization of cell walls within the tissues that border the wound. We sought to characterize the plant's response using a variety of approaches, with a particular focus on lignin deposition within the peripheral fiber cell walls of the stem. Raman spectroscopy and imaging first showed that changes occurred in the polysaccharide matrix of the parenchyma and fiber cell walls. These changes were accompanied by rapid deposition of lignin which initially diffuses centripetally and then, once the vascular cambium was reached, propagates in a periclinal manner until 150 μm from the edges of the wounded zone. Lignin biosynthesis appears to be the result of a <em>de novo</em> activity, as demonstrated by the concomitant accumulation of transcripts corresponding to lignin biosynthesis genes. In addition, using bioorthogonal chemistry approaches, we showed that wounding had enhanced the capacity of fiber cell walls to incorporate modified lignin precursors, in parallel with an increase in transcripts corresponding to peroxidases in the cortical tissues. This incorporation potential was identical for the 3 different types of reporters tested. Our findings demonstrated that mechanical stress can trigger lignification, in a polarized manner within the bast fibers, providing insights into the plasticity of cell wall composition and the potential for modulating fiber properties in flax.</div></div>","PeriodicalId":20234,"journal":{"name":"Plant Physiology and Biochemistry","volume":"223 ","pages":"Article 109806"},"PeriodicalIF":6.1000,"publicationDate":"2025-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Physiology and Biochemistry","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0981942825003341","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
When flax (Linum usitatissimum L.) stems are scarified, major changes occur in the organization of cell walls within the tissues that border the wound. We sought to characterize the plant's response using a variety of approaches, with a particular focus on lignin deposition within the peripheral fiber cell walls of the stem. Raman spectroscopy and imaging first showed that changes occurred in the polysaccharide matrix of the parenchyma and fiber cell walls. These changes were accompanied by rapid deposition of lignin which initially diffuses centripetally and then, once the vascular cambium was reached, propagates in a periclinal manner until 150 μm from the edges of the wounded zone. Lignin biosynthesis appears to be the result of a de novo activity, as demonstrated by the concomitant accumulation of transcripts corresponding to lignin biosynthesis genes. In addition, using bioorthogonal chemistry approaches, we showed that wounding had enhanced the capacity of fiber cell walls to incorporate modified lignin precursors, in parallel with an increase in transcripts corresponding to peroxidases in the cortical tissues. This incorporation potential was identical for the 3 different types of reporters tested. Our findings demonstrated that mechanical stress can trigger lignification, in a polarized manner within the bast fibers, providing insights into the plasticity of cell wall composition and the potential for modulating fiber properties in flax.
期刊介绍:
Plant Physiology and Biochemistry publishes original theoretical, experimental and technical contributions in the various fields of plant physiology (biochemistry, physiology, structure, genetics, plant-microbe interactions, etc.) at diverse levels of integration (molecular, subcellular, cellular, organ, whole plant, environmental). Opinions expressed in the journal are the sole responsibility of the authors and publication does not imply the editors'' agreement.
Manuscripts describing molecular-genetic and/or gene expression data that are not integrated with biochemical analysis and/or actual measurements of plant physiological processes are not suitable for PPB. Also "Omics" studies (transcriptomics, proteomics, metabolomics, etc.) reporting descriptive analysis without an element of functional validation assays, will not be considered. Similarly, applied agronomic or phytochemical studies that generate no new, fundamental insights in plant physiological and/or biochemical processes are not suitable for publication in PPB.
Plant Physiology and Biochemistry publishes several types of articles: Reviews, Papers and Short Papers. Articles for Reviews are either invited by the editor or proposed by the authors for the editor''s prior agreement. Reviews should not exceed 40 typewritten pages and Short Papers no more than approximately 8 typewritten pages. The fundamental character of Plant Physiology and Biochemistry remains that of a journal for original results.