Zhang Chunyu, Zhang Chengyu, Xu Xiaoqiong, Liao Minzhang, Tong Ning, Zhang Zihao, Chen Yukun, Xu Han Xu, Lin Yuling, Lai Zhongxiong
Institute of Horticultural Biotechnology, Fujian Agriculture and Forestry University, Fuzhou, China.
Institut de la Recherche Interdisciplinaire de Toulouse, IRIT-ARI, Toulouse, France.
Front Plant Sci. 2023 Sep 26;14:1255418. doi: 10.3389/fpls.2023.1255418. eCollection 2023.
Cultivated banana are polyploid, with low pollen fertility, and most cultivars are male sterile, which leads to difficulties in banana breeding research. The selection of male parent with excellent resistance and pollen fertility is therefore essential for banana breeding. Wild banana () have developed many good characteristics during natural selection and constitute an excellent gene pool for breeding. Therefore, research on wild banana breeding is very important for banana breeding.
In the current analysis, we examined the changes in viability of wild banana pollens at different temperatures by germination, and found that the germination ability of wild banana pollens cultured at 28°C for 2 days was higher than that of pollens cultured at 23°C (pollens that could not germinate normally under low temperature stress), 24°C (cultured at a constant temperature for 2 days) and 32°C (cultured at a constant temperature for 2 days). To elucidate the molecular mechanisms underlying the germination restoration process in wild banana pollens, we selected the wild banana pollens that had lost its germination ability under low temperature stress (23°C) as the control group (CK) and the wild banana pollens that had recovered its germination ability under constant temperature incubation of 28°C for 2 days as the treatment group (T) for transcriptome sequencing. A total of 921 differentially expressed genes (DEGs) were detected in CK vs T, of which 265 were up-regulated and 656 were down-regulated. The combined analysis of Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) revealed that the activation, metabolism of various substances (lipids, sugars, amino acids) play a major role in restoring pollen germination capacity. TCA cycle and the sesquiterpenoid and triterpenoid biosynthetic pathways were also significantly enriched in the KEGG pathway. And we found that some DEGs may be associated with pollen wall formation, DNA methylation and DNA repair. The cysteine content, free fatty acid (FFA) content, HO content, fructose content, and sucrose content of pollen were increased at treatment of 28°C, while D-Golactose content was decreased. Finally, the GO pathway was enriched for a total of 24 DEGs related to pollen germination, of which 16 DEGs received targeted regulation by 14 MYBs.
Our study suggests that the balance between various metabolic processes, pollen wall remodelling, DNA methylation, DNA repairs and regulation of MYBs are essential for germination of wild banana pollens.
栽培香蕉是多倍体,花粉育性低,且大多数品种雄性不育,这给香蕉育种研究带来了困难。因此,选择具有优良抗性和花粉育性的父本对于香蕉育种至关重要。野生香蕉()在自然选择过程中形成了许多优良特性,构成了优良的育种基因库。因此,野生香蕉育种研究对香蕉育种非常重要。
在当前分析中,我们通过发芽试验检测了野生香蕉花粉在不同温度下的活力变化,发现野生香蕉花粉在28°C培养2天的发芽能力高于在23°C(低温胁迫下不能正常发芽的花粉)、24°C(恒温培养2天)和32°C(恒温培养2天)培养的花粉。为了阐明野生香蕉花粉发芽恢复过程的分子机制,我们选择在低温胁迫(23°C)下失去发芽能力的野生香蕉花粉作为对照组(CK),选择在28°C恒温培养2天恢复发芽能力的野生香蕉花粉作为处理组(T)进行转录组测序。在CK与T组中总共检测到921个差异表达基因(DEG),其中265个上调,656个下调。基因本体论(GO)和京都基因与基因组百科全书(KEGG)的联合分析表明,各种物质(脂质、糖类、氨基酸)的激活、代谢在恢复花粉发芽能力中起主要作用。三羧酸循环以及倍半萜和三萜生物合成途径在KEGG途径中也显著富集。并且我们发现一些DEG可能与花粉壁形成、DNA甲基化和DNA修复有关。在28°C处理时,花粉的半胱氨酸含量、游离脂肪酸(FFA)含量、HO含量、果糖含量和蔗糖含量增加,而D-半乳糖含量降低。最后,GO途径总共富集了24个与花粉发芽相关的DEG,其中16个DEG受到14个MYB的靶向调控。
我们的研究表明,各种代谢过程之间的平衡、花粉壁重塑、DNA甲基化、DNA修复以及MYB的调控对于野生香蕉花粉的发芽至关重要。