Subban Patharajan, Kutsher Yaarit, Evenor Dalia, Belausov Eduard, Zemach Hanita, Faigenboim Adi, Bocobza Samuel, Timko Michael P, Reuveni Moshe
Institute of Plant Sciences, ARO Volcani Center, P.O. Box 15159, Rishon LeZion 7528809, Israel.
Department of Biology, University of Virginia, Charlottesville, VA 22904, USA.
Plants (Basel). 2020 Dec 29;10(1):58. doi: 10.3390/plants10010058.
Shoot regeneration is a key tool of modern plant biotechnology. While many researchers use this process empirically, very little is known about the early molecular genetic factors and signaling events that lead to shoot regeneration. Using tobacco as a model system, we found that the inductive events required for shoot regeneration occur in the first 4-5 days following incubation on regeneration medium. Leaf segments placed on regeneration medium did not produce shoots if removed from the medium before four days indicating this time frame is crucial for the induction of shoot regeneration. Leaf segments placed on regeneration medium for longer than five days maintain the capacity to produce shoots when removed from the regeneration medium. Analysis of gene expression during the early days of incubation on regeneration medium revealed many changes occurring with no single expression pattern evident among major gene families previously implicated in developmental processes. For example, expression of Knotted gene family members increased during the induction period, whereas transcription factors from the Wuschel gene family were unaltered during shoot induction. Expression levels of genes involved in cell cycle regulation increased steadily on regeneration medium while expression of NAC genes varied. No obvious possible candidate genes or developmental processes could be identified as a target for the early events (first few days) in the induction of shoot regeneration. On the other hand, observations during the early stages of regeneration pointed out that regeneration does not occur from a single cell but a group of cells. We observed that while cell division starts just as leaf segments are placed on regeneration medium, only a group of cells could become shoot primordia. Still, these primordia are not identifiable during the first days.
芽再生是现代植物生物技术的一项关键手段。虽然许多研究人员凭经验使用这一过程,但对于导致芽再生的早期分子遗传因素和信号事件却知之甚少。以烟草作为模式系统,我们发现芽再生所需的诱导事件发生在接种到再生培养基后的头4 - 5天内。如果在四天前从培养基中取出,放置在再生培养基上的叶片切段不会产生芽,这表明这段时间对于芽再生的诱导至关重要。放置在再生培养基上超过五天的叶片切段从再生培养基中取出后仍保持产生芽的能力。对在再生培养基上培养早期的基因表达分析显示,发生了许多变化,之前涉及发育过程的主要基因家族中没有明显单一的表达模式。例如,在诱导期,Knotted基因家族成员的表达增加,而Wuschel基因家族的转录因子在芽诱导过程中未发生改变。参与细胞周期调控的基因在再生培养基上的表达水平稳步上升,而NAC基因的表达则有所不同。在芽再生诱导的早期事件(头几天)中,无法确定明显的候选基因或发育过程作为靶点。另一方面,再生早期的观察指出,再生并非从单个细胞而是从一群细胞开始。我们观察到,虽然细胞分裂在叶片切段接种到再生培养基时就开始了,但只有一群细胞能形成芽原基。不过,在最初几天这些芽原基是无法识别的。