Takahashi Wataru, Fujimori Masahiro, Miura Yuichi, Komatsu Toshinori, Nishizawa Yoko, Hibi Tadaaki, Takamizo Tadashi
Forage Crop Research Institute, Japan Grassland Farming and Forage Seed Association, 388-5 Higashiakada, Nishinasuno, Tochigi, 329-2742, Japan.
Plant Cell Rep. 2005 Mar;23(12):811-8. doi: 10.1007/s00299-004-0900-1. Epub 2004 Dec 15.
We introduced the rice chitinase (Cht-2; RCC2) gene into calli of Italian ryegrass (Lolium multiflorum Lam.), with a hygromycin phosphotransferase (HPT) gene as a selectable marker, by particle bombardment. Hygromycin-resistant calli were selected and transferred to regeneration medium for shoot formation. Polymerase chain reaction (PCR) analysis revealed regenerants containing the HPT gene. The RCC2 gene was detected in 65.5% of those regenerants. Southern hybridization detected both HPT and RCC2 genes and indicated that the transgenic plants were independently transformed. Expression of the RCC2 gene in the transgenic plants was confirmed by Northern hybridization, reverse transcription-PCR and Western blotting. Bioassay of detached leaves indicated increased resistance to crown rust (Puccinia coronata) in transgenic plants, which exhibited higher chitinase activity than a nontransgenic plant.
我们通过粒子轰击将水稻几丁质酶(Cht-2;RCC2)基因导入多花黑麦草(Lolium multiflorum Lam.)愈伤组织中,并以潮霉素磷酸转移酶(HPT)基因作为选择标记。筛选出抗潮霉素的愈伤组织并转移至再生培养基上以形成芽。聚合酶链反应(PCR)分析显示再生植株含有HPT基因。在65.5%的再生植株中检测到了RCC2基因。Southern杂交检测到了HPT和RCC2基因,表明转基因植株是独立转化的。通过Northern杂交、逆转录PCR和蛋白质免疫印迹法证实了RCC2基因在转基因植株中的表达。离体叶片生物测定表明转基因植株对冠锈病(Puccinia coronata)的抗性增强,其几丁质酶活性高于非转基因植株。