Zhang Demei, Wang Rui, Han Shijian, Li Zhigang, Xiao Jiming, Li Yangrui, Wang Lingqiang, Li Suli
Guangxi Key Laboratory of Sugarcane Biology, College of Agriculture, Guangxi University, 100 Daxue Rd., Nanning 530004, China.
Guangxi Colleges and Universities Key Laboratory of Crop Cultivation and Tillage, Guangxi University, 100 Daxue Rd., Nanning 530004, China.
Life (Basel). 2022 Aug 9;12(8):1210. doi: 10.3390/life12081210.
Sugarcane somatic cell hybridization can break through the barrier of genetic incompatibility between distantly related species in traditional breeding. However, the molecular mechanisms of sugarcane protoplast regeneration and the conditions for protoplast preparation remain largely unknown. In this study, young sugarcane (ROC22) leaves were enzymatically digested, and the viability of protoplasts reached more than 90% after enzymatic digestion (Enzymatic combination: 2% cellulase + 0.5% pectinase + 0.1% dissociative enzyme + 0.3% hemicellulase, pH = 5.8). Transcriptome sequencing was performed on young sugarcane leaves and protoplasts after enzymatic digestion to analyze the differences in gene expression in somatic cells before and after enzymatic digestion. A total of 117,411 unigenes and 43,460 differentially expressed genes were obtained, of which 21,123 were up-regulated and 22,337 down-regulated. The GO terms for the 43,460 differentially expressed genes (DEGs) were classified into three main categories: biological process, cellular component and molecular function, which related to developmental process, growth, cell proliferation, transcription regulator activity, signal transducer activity, antioxidant activity, oxidative stress, kinase activity, cell cycle, cell differentiation, plant hormone signal transduction, and so on. After enzymatic digestion of young sugarcane leaves, the expressions of , , , , , and genes associated with plant regeneration were significantly down-regulated to 65%, 47%, 2%, 18.60%, 21.32%, 52% and 45% of young leaves, respectively. After enzymatic digestion, / expression was up-regulated compared with young leaves, and / expression was 3.53 times higher than that of young leaves. Compared with young leaves, these key genes were significantly changed after enzymatic digestion. These results indicate that the process of somatic enzymatic digestion process may affect the regeneration of heterozygous cells to a certain extent.
甘蔗体细胞杂交能够突破传统育种中远缘物种间遗传不亲和的障碍。然而,甘蔗原生质体再生的分子机制以及原生质体制备条件在很大程度上仍不清楚。在本研究中,对幼嫩甘蔗(ROC22)叶片进行酶解,酶解后原生质体活力达到90%以上(酶组合:2%纤维素酶+0.5%果胶酶+0.1%离析酶+0.3%半纤维素酶,pH = 5.8)。对幼嫩甘蔗叶片和酶解后的原生质体进行转录组测序,以分析酶解前后体细胞中基因表达的差异。共获得117,411个单基因和43,460个差异表达基因,其中21,123个上调,22,337个下调。43,460个差异表达基因(DEGs)的GO术语分为生物过程、细胞组分和分子功能三大类,涉及发育过程、生长、细胞增殖、转录调节活性、信号转导活性、抗氧化活性、氧化应激、激酶活性、细胞周期、细胞分化、植物激素信号转导等。幼嫩甘蔗叶片酶解后,与植物再生相关的 、 、 、 、 、 和 基因的表达分别显著下调至幼叶的65%、47%、2%、18.60%、21.32%、52%和45%。酶解后, / 表达相对于幼叶上调,且 / 表达比幼叶高3.53倍。与幼叶相比,这些关键基因在酶解后发生了显著变化。这些结果表明,体细胞酶解过程可能在一定程度上影响杂种细胞的再生。