Jiang J, Wing V, Xiet T, Shi X, Wang Y P, Sokolov V
Genetika. 2016 Jan;52(1):66-73. doi: 10.7868/s0016675816010082.
Soybean is recognized as one of the plants which are very difficult to be transformed. Considering the low transformation efficiency of soybean, we aimed to determine the effect of 6-benzylaminopurine (6-BA), shoot induction time, and infection time of Agrobacterium on the clonal propagation of Glycine max. Results showed that 1.6 mg/L 6-BA could be optimal to promote the induction of adventitious shoots. An induction time of 15 d was considered optimal for the actual experiment involving soybean shoot induction. Agrobacterium was cultured until an OD600 = 0.8 was reached for an infection time of 30 min; this infection time may be optimal to promote soybean transformation. Whole genome DNA methylation was analyzed by high-performance liquid chromatography (HPLC)-assisted quantification, and DNA methylation result is consistent with the phenotypic data of shoot development. In addition, two methylation-related genes (Decrease in DNA methylation 1 and DNA methyltransferases chromomethylase 2) were analyzed to determine expression differences by qRT-PCR in the shoots that were developed under different experimental conditions. In general, the expression values of these genes were normally downregulated under the recommended experimental conditions of soybean regeneration. This study showed the overall methylation changes in the in vitro culture of soybean, as affected by several variable parameters, which is useful to promote the transformation efficiency of soybean.
大豆被认为是极难转化的植物之一。鉴于大豆的转化效率较低,我们旨在确定6-苄基腺嘌呤(6-BA)、芽诱导时间和农杆菌感染时间对大豆克隆繁殖的影响。结果表明,1.6 mg/L的6-BA最有利于促进不定芽的诱导。对于涉及大豆芽诱导的实际实验,15天的诱导时间被认为是最佳的。将农杆菌培养至OD600 = 0.8,感染时间为30分钟;这个感染时间可能最有利于促进大豆转化。通过高效液相色谱(HPLC)辅助定量分析全基因组DNA甲基化,DNA甲基化结果与芽发育的表型数据一致。此外,分析了两个与甲基化相关的基因(DNA甲基化减少1和DNA甲基转移酶染色质甲基化酶2),通过qRT-PCR确定在不同实验条件下发育的芽中的表达差异。总体而言,在大豆再生的推荐实验条件下,这些基因的表达值通常下调。本研究显示了大豆离体培养中受几个可变参数影响的总体甲基化变化,这有助于提高大豆的转化效率。