Han Xiao-Ling, Bu Huai-Yu, Hao Jian-Guo, Zhao Yu-Wei, Jia Jing-Fen
College of Life Science, Northwest University, Xi'an 710069, China.
Sheng Wu Gong Cheng Xue Bao. 2006 Jan;22(1):107-13.
An efficient system of genetic transformation and plant regeneration via somatic embryogenesis was established in crownvetch (Coronilla varia L.) by infecting the segments of cotyledons and hypocotyls of 15d-old seedlings with Agrobacterium rhizogenes strain 15834. Hairy roots were produced directly from the wounded surface of the explants or via calluses on hormone-free Murashige and Skoog (MS) medium after infection by A. rhizogenes. Transformed roots grew rapidly either on solid or liquid MS medium, and exhibited typical hairy root phenotypes. The highest transformation frequency (87.4%) was achieved by preculturing cotyledons for 2d and pre-treating the A. rhizogenes with suitable concentration of acetosyringone at logarithmic phase (OD600 = 0.8). The embryogenic calluses with 100% induction frequency were induced from hairy roots on MS medium containing 0.2mg/L 2,4-D, 0.5mg/L NAA and 0.5mg/L KT. Globular-, heart-, torpedo-, and cotyledon shaped somatic embryos were produced orderly and developed into plantlets when transferred the embryogenic calluses on MS medium supplemented with 0.5mg/L KT, 0.2mg/L IBA and 300mg/L proline. The transformed plants did not show differences in morphology except abundant lateral root branches compared to the non-transformed plants. However, the contents of 3-nitropropanic acid in hairy roots and leaves of one of 5 transformed clones were 57.68% and 58.17% in roots and leaves of untransformed plants, respectively. Opine paper electrophoresis revealed the integration and expression of TR-DNA. PCR analysis confirmed that the TL-DNA including 654 bp rol B sequence was inserted into the genome of transformed hairy roots and their regenerated plants.
通过用发根农杆菌菌株15834感染15日龄幼苗的子叶和下胚轴切段,在小冠花(Coronilla varia L.)中建立了一种通过体细胞胚胎发生进行遗传转化和植株再生的高效系统。发根农杆菌感染后,毛状根直接从外植体的伤口表面产生,或在无激素的Murashige和Skoog(MS)培养基上通过愈伤组织产生。转化根在固体或液体MS培养基上生长迅速,并表现出典型的毛状根表型。通过将子叶预培养2天,并在对数期(OD600 = 0.8)用合适浓度的乙酰丁香酮预处理发根农杆菌,获得了最高转化频率(87.4%)。在含有0.2mg/L 2,4-D、0.5mg/L NAA和0.5mg/L KT的MS培养基上,从毛状根诱导出诱导频率为100%的胚性愈伤组织。当将胚性愈伤组织转移到添加有0.5mg/L KT、0.2mg/L IBA和300mg/L脯氨酸的MS培养基上时,依次产生球形、心形、鱼雷形和子叶形体细胞胚,并发育成植株。与未转化植株相比,转化植株除侧根分支丰富外,形态上没有差异。然而,5个转化克隆之一的毛状根和叶片中3-硝基丙酸的含量分别是未转化植株根和叶中含量的57.68%和58.17%。冠瘿碱纸电泳显示TR-DNA的整合和表达。PCR分析证实,包含654 bp rol B序列的TL-DNA插入到了转化毛状根及其再生植株的基因组中。