Ravanfar Seyed Ali, Aziz Maheran Abdul, Saud Halimi Mohd, Abdullah Janna Ong
Department of Agriculture Technology, Faculty of Agriculture, Universiti Putra Malaysia, 43400, Serdang, Selangor Darul Ehsan, Malaysia.
Laboratory of Plantation Crops, Institute of Tropical Agriculture, Universiti Putra Malaysia, 43400, Serdang, Selangor Darul Ehsan, Malaysia.
Curr Genet. 2015 Nov;61(4):653-63. doi: 10.1007/s00294-015-0494-x. Epub 2015 May 19.
An efficient system for shoot regeneration and Agrobacterium tumefaciens-mediated transformation of Brassica oleracea cv. Green Marvel cultivar is described. This study focuses on developing shoot regeneration from hypocotyl explants of broccoli cv. Green Marvel using thidiazuron (TDZ), zeatin, and kinetin, the optimization of factors affecting Agrobacterium-mediated transformation of the hypocotyl explants with heat-resistant cDNA, followed by the confirmation of transgenicity of the regenerants. High shoot regeneration was observed in 0.05-0.1 mg dm(-3) TDZ. TDZ at 0.1 mg dm(-3) produced among the highest percentage of shoot regeneration (96.67 %) and mean number of shoot formation (6.17). The highest percentage (13.33 %) and mean number (0.17) of putative transformant production were on hypocotyl explants subjected to preculture on shoot regeneration medium (SRM) with 200 µM acetosyringone. On optimization of bacterial density and inoculation time, the highest percentage and mean number of putative transformant production were on hypocotyl explants inoculated with a bacterial dilution of 1:5 for 30 min. Polymerase chain reaction (PCR) assay indicated a transformation efficiency of 8.33 %. The luciferase assay showed stable integration of the Arabidopsis thaliana HSP101 (AtHSP101) cDNA in the transgenic broccoli regenerants. Three out of five transgenic lines confirmed through PCR showed positive hybridization bands of the AtHSP101 cDNA through Southern blot analysis. The presence of AtHSP101 transcripts in the three transgenic broccoli lines indicated by reverse transcription-PCR (RT-PCR) confirmed the expression of the gene. In conclusion, an improved regeneration system has been established from hypocotyl explants of broccoli followed by successful transformation with AtHSP101 for resistance to high temperature.
描述了一种用于甘蓝型油菜品种“绿色奇迹”的高效芽再生及根癌农杆菌介导转化的系统。本研究着重于利用噻二唑素(TDZ)、玉米素和激动素从西兰花品种“绿色奇迹”的下胚轴外植体诱导芽再生,优化影响下胚轴外植体与耐热cDNA进行农杆菌介导转化的因素,随后确认再生植株的转基因性。在0.05 - 0.1 mg dm(-3) TDZ中观察到高芽再生率。0.1 mg dm(-3)的TDZ产生了最高的芽再生百分比(96.67%)和平均芽形成数(6.17)。在含有200 μM乙酰丁香酮的芽再生培养基(SRM)上预培养的下胚轴外植体上,推定转化体产生的最高百分比(13.33%)和平均数(0.17)。在优化细菌密度和接种时间后,用1:5的细菌稀释液接种30分钟的下胚轴外植体上,推定转化体产生的百分比和平均数最高。聚合酶链反应(PCR)分析表明转化效率为8.33%。荧光素酶测定表明拟南芥热激蛋白101(AtHSP101)cDNA在转基因西兰花再生植株中稳定整合。通过PCR确认的五个转基因株系中有三个通过Southern印迹分析显示出AtHSP101 cDNA的阳性杂交带。逆转录PCR(RT-PCR)表明三个转基因西兰花株系中存在AtHSP101转录本,证实了该基因的表达。总之,已从西兰花的下胚轴外植体建立了改进的再生系统,随后成功用AtHSP101进行转化以获得高温抗性。