Beijing Advanced Innovation Center for Tree Breeding by Molecular Design, National Engineering Laboratory for Tree Breeding, Key Laboratory of Genetics and Breeding in Forest Trees and Ornamental Plants, Ministry of Education, College of Biological Sciences and Technology, Beijing Forestry University, Beijing 100083, China.
Institute of Forest Genetics and Tree Breeding, Shanxi Academy of Forestry and Grassland Sciences, Taiyuan 030012, China.
Int J Mol Sci. 2021 Dec 7;22(24):13200. doi: 10.3390/ijms222413200.
Cellulose synthesis is a complex process in plant cells that is important for wood processing, pulping, and papermaking. Cellulose synthesis begins with the glycosylation of sitosterol by sitosterol glycosyltransferase (SGT) to produce sitosterol-glucoside (SG), which acts as the guiding primer for cellulose production. However, the biological functions of SGTs in remain largely unknown. Two full-length genes ( and ) were previously isolated from and characterized. In the present study, CRISPR/Cas9 gene-editing technology was used to construct sgRNA and sgRNA expression vectors, which were genetically transformed into using the -mediated method to obtain transgenic lines. Nucleic acid and amino acid sequencing analysis revealed both base insertions and deletions, in addition to reading frame shifts and early termination of translation in the transgenic lines. Sugar metabolism analysis indicated that sucrose and fructose were significantly downregulated in stems and leaves of mutant 1 and 1. Glucose levels did not change significantly in roots and stems of 1 mutants; however, glucose was significantly upregulated in stems and downregulated in leaves of the 1 mutants. Dissection of the plants revealed disordered and loosely arranged xylem cells in the 1 mutant, which were larger and thinner than those of the wild-type. This work will enhance our understanding of cellulose synthesis in the cell walls of woody plants.
纤维素合成是植物细胞中的一个复杂过程,对于木材加工、制浆和造纸都非常重要。纤维素合成始于甾醇通过甾醇糖基转移酶(SGT)的糖基化作用生成甾醇葡萄糖苷(SG),SG 作为纤维素产生的引导引物。然而,SGT 在 中的生物学功能在很大程度上仍然未知。先前从 中分离出两个全长 基因(和),并对其进行了表征。在本研究中,使用 CRISPR/Cas9 基因编辑技术构建 sgRNA 和 sgRNA 表达载体,通过介导的方法将其遗传转化到 中,获得转基因株系。核酸和氨基酸测序分析表明,在转基因株系中不仅发生了碱基插入和缺失,还发生了阅读框移位和翻译提前终止。糖代谢分析表明,突变体 1 和 1 的茎和叶中的蔗糖和果糖显著下调。1 突变体根和茎中的葡萄糖水平没有明显变化;然而,1 突变体的茎中葡萄糖显著上调,叶中葡萄糖显著下调。对植物进行解剖发现,1 突变体的木质部细胞排列紊乱且松散,其细胞比野生型更大、更薄。这项工作将增进我们对木质部细胞壁中纤维素合成的理解。