He Haihao, Xu Junfei, Cai Nianhui, Xu Yulan
Key Laboratory of Forest Resources Conservation and Utilization in the Southwest Mountains of China, Ministry of Education, Southwest Forestry University, Kunming, Yunnan Province, China.
Laboratory of National Forestry and Grassland Administration on Biodiversity Conservation in Southwest China, Southwest Forestry University, Kunming, Yunnan Province, China.
BMC Plant Biol. 2024 Dec 20;24(1):1219. doi: 10.1186/s12870-024-05819-6.
P. yunnanensis, a distinctive economic tree species native to Yunnan Province in China, possesses axillary buds that serve as superior material for asexual propagation. However, under natural growth conditions, the differentiation of these axillary buds is notably scarce. In this study, we employed decapitation to stimulate the development of axillary buds in P. yunnanensis. Subsequently, we assessed the phytohormone levels in both axillary and apical buds, and conducted a comprehensive transcriptomic analysis complemented by RT-qPCR validation.
We found that decapitation could effectively promote the releases of the axillary buds in P. yunnanensis. The levels of cytokinin, auxin, gibberellin and abscisic acid in axillary buds were higher than those in apical buds, and the difference in gibberellin levels was the greatest. The transcriptome sequencing results were highly reproducible, and the relative expression levels of the 13 genes screened were highly consistent with the FPKM value trend of transcriptome sequencing. There were 2877 differentially expressed genes (DEGs) between axillary buds and terminal buds, and 18 candidate genes (CGs) involved in axillary bud release were screened out. A total of 1171 DEGs were identified during the analysis of axillary bud growth, and 14 CGs involved in axillary bud growth and development were screened out. GO and KEGG enrichment analysis were performed on the DEGs. Furthermore, combined with the results and discussion, the functions of the candidate genes were analyzed and a possible regulatory network was constructed.
The findings and discussions indicated that the development of axillary buds in P. yunnanensis is predominantly governed by cytokinin, gibberellin, strigolactone, and auxin, as well as their biosynthesis and regulatory genes, which are crucial to the development of these buds. This study has, to some extent, bridged the research gap concerning the development of axillary buds in P. yunnanensis and has provided foundational data to support further research into the developmental mechanisms of these buds and the establishment of asexual propagation cutting nurseries.
云南松是中国云南省特有的一种经济树种,其腋芽是无性繁殖的优质材料。然而,在自然生长条件下,这些腋芽的分化极为稀少。在本研究中,我们采用去顶处理来刺激云南松腋芽的发育。随后,我们评估了腋芽和顶芽中的植物激素水平,并进行了全面的转录组分析,辅以RT-qPCR验证。
我们发现去顶处理能够有效促进云南松腋芽的萌发。腋芽中细胞分裂素、生长素、赤霉素和脱落酸的水平高于顶芽,其中赤霉素水平的差异最为显著。转录组测序结果具有高度可重复性,筛选出的13个基因的相对表达水平与转录组测序的FPKM值趋势高度一致。腋芽和顶芽之间有2877个差异表达基因(DEGs),并筛选出18个参与腋芽萌发的候选基因(CGs)。在腋芽生长分析过程中,共鉴定出1171个DEGs,并筛选出14个参与腋芽生长发育的CGs。对这些DEGs进行了GO和KEGG富集分析。此外,结合结果与讨论,分析了候选基因的功能并构建了一个可能的调控网络。
研究结果表明,云南松腋芽的发育主要受细胞分裂素、赤霉素、独脚金内酯和生长素及其生物合成和调控基因的控制,这些对腋芽的发育至关重要。本研究在一定程度上弥补了云南松腋芽发育研究的空白,并为进一步研究这些芽的发育机制和建立无性繁殖扦插苗圃提供了基础数据。