Manipulation of the brown glume and internode 1 gene leads to alterations in the colouration of lignified tissues, lignin content and pathogen resistance in wheat

Summary Lignin is a crucial component of the cell wall, providing mechanical support and protection against biotic and abiotic stresses. However, little is known about wheat lignin‐related mutants and their roles in pathogen defence. Here, we identified an ethyl methanesulfonate (EMS)‐derived Aegilops tauschii mutant named brown glume and internode 1 ( bgi1 ), which exhibits reddish‐brown pigmentation in various tissues, including internodes, spikes and glumes. Using map‐based cloning and single nucleotide polymorphism (SNP) analysis, we identified AET6Gv20438400 ( BGI1 ) as the leading candidate gene, encoding the TaCAD1 protein. The mutation occurred in the splice acceptor site of the first intron, resulting in a premature stop codon in BGI1 . We validated the function of BGI1 using loss‐of‐function EMS and gene editing knockout mutants, both of which displayed reddish‐brown pigmentation in lignified tissues. BGI1 knockout mutants exhibited reduced lignin content and shearing force relative to wild type, while BGI1 overexpression transgenic plants showed increased lignin content and enhanced disease resistance against common root rot and Fusarium crown rot. We confirmed that BGI1 exhibits CAD activity both in vitro and in vivo , playing an important role in lignin biosynthesis. BGI1 was highly expressed in the stem and spike, with its localisation observed in the cytoplasm. Transcriptome analysis revealed the regulatory networks associated with BGI1 . Finally, we demonstrated that BGI1 interacts with TaPYL‐1D, potentially involved in the abscisic acid signalling pathway. The identification and functional characterisation of BGI1 significantly advance our understanding of CAD proteins in lignin biosynthesis and plant defence against pathogen infection in wheat.