Guo Mengjie, Wang Ruxia, Wang Bo, Xu Wenjing, Hou Hui, Cheng Hao, Zhang Yun, Wang Chong, Cheng Yuxiang
State Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, Harbin 150040, China.
College of Life Sciences, Northeast Forestry University, Harbin 150040, China.
Plants (Basel). 2025 Jun 25;14(13):1948. doi: 10.3390/plants14131948.
Wood is an important raw material for industrial applications. Its fiber-specific genetic modification provides an effective strategy to alter wood characteristics in tree breeding. Here, we performed a cross-analysis of previously reported single-cell RNA sequencing and the AspWood database during wood formation to identify potential xylem fiber-dominant expressing genes in poplar. As a result, 32 candidate genes were obtained, and subsequently, we further examined the expression of these genes in fibers and/or vessels of stem secondary xylem using the laser capture microdissection technique and RT-qPCR. Analysis identified nine candidate genes, including , , , , , , , , and . Next, we cloned the promoter regions of the nine candidate genes and created promoter::GUS transgenic poplars. Histochemical GUS staining was used to investigate the tissue expression activities of these gene promoters in transgenic poplars. In one month, transgenic plantlets grown in medium showed intensive GUS staining signals that were visible in the leaves and apical buds, suggesting substantial expression activities of these gene promoters in plantlets predominantly undergoing primary growth. In contrast, for three-month-old transgenic poplars in the greenhouse with predominantly developed secondary stem tissues, the promoters of seven of nine candidate genes, including , , and , showed secondary xylem fiber-dominant GUS signals with considerable spatial specificity. Overall, this study presents xylem fiber-dominant promoters that are well-suited for specifically expressing genes of interest in wood fibers for forest tree breeding.
木材是工业应用的重要原材料。其纤维特异性基因改造为树木育种中改变木材特性提供了一种有效策略。在此,我们在木材形成过程中对先前报道的单细胞RNA测序和AspWood数据库进行了交叉分析,以鉴定杨树中潜在的木质部纤维优势表达基因。结果,获得了32个候选基因,随后,我们使用激光捕获显微切割技术和RT-qPCR进一步检测了这些基因在茎次生木质部纤维和/或导管中的表达。分析鉴定出9个候选基因,包括 、 、 、 、 、 、 、 和 。接下来,我们克隆了这9个候选基因的启动子区域,并创建了启动子::GUS转基因杨树。利用组织化学GUS染色研究了这些基因启动子在转基因杨树中的组织表达活性。在一个月大时,在培养基中生长的转基因幼苗显示出强烈的GUS染色信号,在叶片和顶芽中可见,表明这些基因启动子在主要经历初生生长的幼苗中具有大量表达活性。相比之下,对于温室中三个月大的主要发育出次生茎组织的转基因杨树,9个候选基因中的7个,包括 、 和 ,其启动子显示出具有相当空间特异性的次生木质部纤维优势GUS信号。总体而言,本研究提出了木质部纤维优势启动子,非常适合在林木育种中在木纤维中特异性表达感兴趣的基因。