Tan Hwei-Ting, Shirley Neil J, Singh Rohan R, Henderson Marilyn, Dhugga Kanwarpal S, Mayo Gwenda M, Fincher Geoffrey B, Burton Rachel A
BMC Plant Biol. 2015 Feb 21;15:62. doi: 10.1186/s12870-015-0448-y.
The ability to increase cellulose content and improve the stem strength of cereals could have beneficial applications in stem lodging and producing crops with higher cellulose content for biofuel feedstocks. Here, such potential is explored in the commercially important crop barley through the manipulation of cellulose synthase genes (CesA).
Barley plants transformed with primary cell wall (PCW) and secondary cell wall (SCW) barley cellulose synthase (HvCesA) cDNAs driven by the CaMV 35S promoter, were analysed for growth and morphology, transcript levels, cellulose content, stem strength, tissue morphology and crystalline cellulose distribution. Transcript levels of the PCW HvCesA transgenes were much lower than expected and silencing of both the endogenous CesA genes and introduced transgenes was often observed. These plants showed no aberrant phenotypes. Although attempts to over-express the SCW HvCesA genes also resulted in silencing of the transgenes and endogenous SCW HvCesA genes, aberrant phenotypes were sometimes observed. These included brittle nodes and, with the 35S:HvCesA4 construct, a more severe dwarfing phenotype, where xylem cells were irregular in shape and partially collapsed. Reductions in cellulose content were also observed in the dwarf plants and transmission electron microscopy showed a significant decrease in cell wall thickness. However, there were no increases in overall crystalline cellulose content or stem strength in the CesA over-expression transgenic plants, despite the use of a powerful constitutive promoter.
The results indicate that the cellulose biosynthetic pathway is tightly regulated, that individual CesA proteins may play different roles in the synthase complex, and that the sensitivity to CesA gene manipulation observed here suggests that in planta engineering of cellulose levels is likely to require more sophisticated strategies.
提高谷物纤维素含量并增强茎秆强度的能力,在防止茎倒伏以及培育纤维素含量更高的作物作为生物燃料原料方面可能具有有益的应用。在此,通过对纤维素合酶基因(CesA)的操控,在具有重要商业价值的作物大麦中探索了这种潜力。
对用花椰菜花叶病毒35S启动子驱动的初级细胞壁(PCW)和次级细胞壁(SCW)大麦纤维素合酶(HvCesA)cDNA转化的大麦植株,进行了生长与形态、转录水平、纤维素含量、茎秆强度、组织形态以及结晶纤维素分布的分析。PCW HvCesA转基因的转录水平远低于预期,并且经常观察到内源CesA基因和导入的转基因均发生沉默。这些植株未表现出异常表型。尽管试图过表达SCW HvCesA基因也导致转基因和内源SCW HvCesA基因沉默,但有时会观察到异常表型。这些表型包括脆节,以及用35S:HvCesA4构建体转化时出现的更严重的矮化表型,其中木质部细胞形状不规则且部分塌陷。在矮化植株中还观察到纤维素含量降低,透射电子显微镜显示细胞壁厚度显著减小。然而,尽管使用了强大的组成型启动子,CesA过表达转基因植株的整体结晶纤维素含量或茎秆强度并未增加。
结果表明纤维素生物合成途径受到严格调控,单个CesA蛋白可能在合酶复合体中发挥不同作用,并且此处观察到的对CesA基因操控的敏感性表明,在植物中对纤维素水平进行工程改造可能需要更复杂的策略。