State Key Laboratory of Subtropical Silviculture, Sino-Australia Plant Cell Wall Research Centre, College of Forestry and Biotechnology, Zhejiang A&F University, Hangzhou, Zhejiang 311300, China.
State Key Laboratory of Subtropical Silviculture, Sino-Australia Plant Cell Wall Research Centre, College of Forestry and Biotechnology, Zhejiang A&F University, Hangzhou, Zhejiang 311300, China.
Plant Sci. 2024 Jul;344:112083. doi: 10.1016/j.plantsci.2024.112083. Epub 2024 Apr 6.
Due to the extended generation cycle of trees, the breeding process for forest trees tends to be time-consuming. Genetic engineering has emerged as a viable approach to expedite the genetic breeding of forest trees. However, current genetic engineering techniques employed in forest trees often utilize continuous expression promoters such as CaMV 35S, which may result in unintended consequences by introducing genes into non-target tissues. Therefore, it is imperative to develop specific promoters for forest trees to facilitate targeted and precise design and breeding. In this study, we utilized single-cell RNA-Seq data and co-expression network analysis during wood formation to identify three vascular tissue-specific genes in poplar, PP2-A10, PXY, and VNS07, which are expressed in the phloem, cambium/expanding xylem, and mature xylem, respectively. Subsequently, we cloned the promoters of these three genes from '84K' poplar and constructed them into a vector containing the eyGFPuv visual selection marker, along with the 35S mini enhancer to drive GUS gene expression. Transgenic poplars expressing the Pro::GUS, Pro::GUS, and Pro::GUS constructs were obtained. To further elucidate the tissue specificity of these promoters, we employed qPCR, histochemical staining, and GUS enzyme activity. Our findings not only establish a solid foundation for the future utilization of these promoters to precisely express of specific functional genes in stems but also provide a novel perspective for the modular breeding of forest trees.
由于树木的世代周期较长,因此林木的育种过程往往比较耗时。遗传工程已成为加速林木遗传育种的可行方法。然而,当前林木遗传工程中常用的技术通常利用 CaMV 35S 等持续表达启动子,将基因引入非目标组织可能会带来意想不到的后果。因此,开发林木专用启动子对于实现靶向、精准设计和育种至关重要。在这项研究中,我们利用木材形成过程中的单细胞 RNA-Seq 数据和共表达网络分析,在杨树中鉴定了三个血管组织特异性基因,即 PP2-A10、PXY 和 VNS07,它们分别在韧皮部、形成层/扩展木质部和成熟木质部中表达。随后,我们从“84K”杨树中克隆了这三个基因的启动子,并将其构建到一个载体中,该载体包含 eyGFPuv 视觉选择标记和 35S 迷你增强子,以驱动 GUS 基因表达。获得了表达 Pro::GUS、Pro::GUS 和 Pro::GUS 构建体的转基因杨树。为了进一步阐明这些启动子的组织特异性,我们进行了 qPCR、组织化学染色和 GUS 酶活性分析。我们的研究结果不仅为将来利用这些启动子精确表达茎部特定功能基因奠定了基础,也为林木的模块化育种提供了新的视角。