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BRITTLE CULM17, a Novel Allele of TAC4, Affects the Mechanical Properties of Rice Plants

文献类型： 外文期刊

作者： Li, Guangzheng 1 ; Zeng, Xiaofang 2 ; Li, Yan 2 ; Li, Jianrong 2 ; Huang, Xiaozhen 2 ; Zhao, Degang 1 ;

作者机构： 1.Guizhou Univ, Ctr Res & Dev Fine Chem, State Key Lab Green Pesticide & Agr Biol Engn, Guiyang 550025, Peoples R China

2.Guizhou Univ, Key Lab Plant Resources Conservat & Germplasm Inn, Minist Educ, Inst Agrobioengn,Coll Life Sci, Guiyang 550025, Peoples R China

3.Guizhou Acad Agr Sci, Guizhou Plant Conservat Ctr, Guiyang 550006, Peoples R China

关键词： Guizhou landrace rice; brittle stem mutant; gene mapping; gene functional analysis

期刊名称：INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES （ 影响因子：6.208； 五年影响因子：6.628 ）

ISSN：

年卷期： 2022 年 23 卷 10 期

页码：

收录情况： SCI

摘要： Lodging resistance of rice (Oryza sativa L.) has always been a hot issue in agricultural production. A brittle stem mutant, osbc17, was identified by screening an EMS (Ethylmethane sulfonate) mutant library established in our laboratory. The stem segments and leaves of the mutant were obviously brittle and fragile, with low mechanical strength. Examination of paraffin sections of flag leaf and internode samples indicated that the number of cell layers in mechanical tissue of the mutant was decreased compared with the wild type, Pingtangheinuo, and scanning electron microscopy revealed that the mechanical tissue cell walls of the mutant were thinner. Lignin contents of the internodes of mature-stage rice were significantly lower in the mutant than in the wild type. By the MutMap method, we found candidate gene OsBC17, which was located on rice chromosome 2 and had a 2433 bp long coding sequence encoding a protein sequence of 810 amino acid residues with unknown function. According to LC-MS/MS analysis of intermediate products of the lignin synthesis pathway, the accumulation of caffeyl alcohol in the osbc17 mutant was significantly higher than in Pingtangheinuo. Caffeyl alcohol can be polymerized to the catechyl lignin monomer by laccase ChLAC8; however, ChLAC8 and OsBC17 are not homologous proteins, which suggests that the osbc17 gene is involved in this process by regulating laccase expression.

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