Fang Siyu, Li Jie, Zheng Wenfeng, Liu Zhiyong, Feng Hui, Zhang Yun
College of Horticulture, Shenyang Agricultural University, Shenyang, 110866, People's Republic of China.
Key Laboratory of Cruciferous Vegetable Genetics and Breeding of Liaoning Province, Shenyang Agricultural University, Shenyang, 110866, People's Republic of China.
Protoplasma. 2023 Jan;260(1):225-236. doi: 10.1007/s00709-022-01771-0. Epub 2022 May 16.
Isolated microspore culture has been implemented in breeding programs to produce doubled haploid (DH) lines and thus accelerates the breeding process. However, low microspore embryogenesis frequency in flowering Chinese cabbage remains a key obstacle to the practical application of this technique. This study aimed to establish an efficient microspore culture protocol for flowering Chinese cabbage that would be applied for heterosis breeding. Microspores of five genotypes, 19AY05, 19AY06, 19AY10, 19AY12, and 19AY15, were successfully induced to produce embryos in NLN-13 medium. Microspores of two genotypes, 19AY05 and 19AY15, were cultivated in NLN-13 medium supplemented with different concentrations (0, 0.01, 0.05, 0.1, or 0.2 mg·L) of compound sodium nitrophenol (sodium nitrophenol, 5-nitrophenol) to enhance microspore embryogenesis and plant regeneration without an intervening callus phase. The results showed that 0.05 ~ 0.1 mg· L sodium nitrophenol and 0.01 ~ 0.2 mg· L of 5-nitrophenol significantly promoted the induction of microspore embryogenesis of two genotypes, and the best concentrations required for different genotypes are different. Moreover, 0.1 mg· L sodium nitrophenol can significantly increase the plant regeneration rate of the two genetypes. The 5-nitrophenol at 0.01 mg·L significantly increased rate of embryos directly convert to plant in 19AY15. In addition, the average doubled haploid rates in the five genotypes were close to 63%. Horticultural traits of DH lines from 19AY05 were identified and all of them were self-incompatible lines. They showed a high uniformity and consistency that can be directly used for hybrid breeding. Furthermore, the hybrid combination was prepared with the selected DH lines and the Guangdong nucleus genic sterile line GMS019 to screen the excellent hybrid combination for the flowering Chinese cabbage breeding program. This method accelerates the application of microspore culture in hybrid breeding of flowering Chinese cabbage.
游离小孢子培养已应用于育种计划,以产生双单倍体(DH)系,从而加速育种进程。然而,青花菜小孢子胚胎发生频率较低仍然是该技术实际应用的关键障碍。本研究旨在建立一种高效的青花菜小孢子培养方案,用于杂种优势育种。19AY05、19AY06、19AY10、19AY12和19AY15这5个基因型的小孢子在NLN-13培养基中成功诱导产生胚。19AY05和19AY15这两个基因型的小孢子在添加不同浓度(0、0.01、0.05、0.1或0.2mg·L)间硝基苯酚钠(间硝基苯酚、5-硝基苯酚)的NLN-13培养基中培养,以提高小孢子胚胎发生和植株再生能力,无需经过愈伤组织阶段。结果表明,0.05~0.1mg·L间硝基苯酚钠和0.01~0.2mg·L的5-硝基苯酚显著促进了两个基因型小孢子胚胎发生的诱导,不同基因型所需的最佳浓度不同。此外,0.1mg·L间硝基苯酚钠能显著提高两个基因型的植株再生率。0.01mg·L的5-硝基苯酚显著提高了19AY15中胚直接转化为植株的比率。此外,5个基因型的平均双单倍体率接近63%。对19AY05的DH系园艺性状进行了鉴定,结果表明它们均为自交不亲和系。它们表现出高度的均匀性和一致性,可直接用于杂交育种。此外,用筛选出的DH系与广东细胞核雄性不育系GMS019配制杂交组合,筛选出青花菜育种优良杂交组合。该方法加速了小孢子培养在青花菜杂交育种中的应用。