Laboratoire de Recherche en Sciences Végétales, Université de Toulouse III, CNRS, UPS, UMR 5546, 24 Chemin de Borde Rouge, 31320 Castanet-Tolosan, France.
UMR 990, Génomique et Biotechnologie des Fruits, Université de Toulouse, INP-ENSA Toulouse, Avenue de l'Agrobiopole, 31326 Castanet-Tolosan, France.
Int J Mol Sci. 2020 May 12;21(10):3408. doi: 10.3390/ijms21103408.
Eucalypts are the most planted hardwoods worldwide. The availability of the genome highlighted many genes awaiting functional characterization, lagging behind because of the lack of efficient genetic transformation protocols. In order to efficiently generate knock-out mutants to study the function of eucalypts genes, we implemented the powerful CRISPR/Cas9 gene editing technology with the hairy roots transformation system. As proofs-of-concept, we targeted two wood-related genes: (), a key lignin biosynthetic gene and an auxin dependent transcription factor of family. Almost all transgenic hairy roots were edited but the allele-editing rates and spectra varied greatly depending on the gene targeted. Most edition events generated truncated proteins, the prevalent edition types were small deletions but large deletions were also quite frequent. By using a combination of FT-IR spectroscopy and multivariate analysis (partial least square analysis (PLS-DA)), we showed that the -edited lines, which were clearly separated from the controls. The most discriminant wave-numbers were attributed to lignin. Histochemical analyses further confirmed the decreased lignification and the presence of collapsed vessels in -edited lines, which are characteristics of deficiency. Although the efficiency of editing could be improved, the method described here is already a powerful tool to functionally characterize eucalypts genes for both basic research and industry purposes.
桉树是全球种植最广泛的硬木树种。基因组的可用性凸显了许多等待功能表征的基因,由于缺乏有效的遗传转化方案,这些基因的研究一直滞后。为了有效地生成敲除突变体来研究桉树基因的功能,我们将强大的 CRISPR/Cas9 基因编辑技术与毛状根转化系统相结合。作为概念验证,我们针对两个与木材相关的基因:(),一个关键的木质素生物合成基因和 一个生长素依赖的 家族转录因子。几乎所有的转基因毛状根都被编辑了,但等位基因编辑率和谱因靶基因而异而有很大差异。大多数编辑事件产生截断蛋白,常见的编辑类型是小缺失,但大缺失也相当频繁。通过使用傅里叶变换红外光谱和多元分析(偏最小二乘分析(PLS-DA)),我们表明 - 编辑的品系与对照明显分离。最具鉴别力的波数归因于木质素。组织化学分析进一步证实了 - 编辑品系中木质化程度降低和血管壁塌陷的存在,这是 缺乏的特征。尽管编辑效率可以提高,但这里描述的方法已经是一种强大的工具,可以用于桉树基因的功能表征,无论是基础研究还是工业目的。