Plant Molecular and Cellular Genetics, Bose Institute, Centenary Campus, P1/12 CIT Scheme VII M, Kankurgachi, Kolkata, 700054, India.
Plant Cell Rep. 2010 Mar;29(3):261-71. doi: 10.1007/s00299-010-0819-7. Epub 2010 Jan 22.
Rice, the major food crop of world is severely affected by homopteran sucking pests. We introduced coding sequence of Allium sativum leaf agglutinin, ASAL, in rice cultivar IR64 to develop sustainable resistance against sap-sucking planthoppers as well as eliminated the selectable antibiotic-resistant marker gene hygromycin phosphotransferase (hpt) exploiting cre/lox site-specific recombination system. An expression vector was constructed containing the coding sequence of ASAL, a potent controlling agent against green leafhoppers (GLH, Nephotettix virescens) and brown planthopper (BPH, Nilaparvata lugens). The selectable marker (hpt) gene cassette was cloned within two lox sites of the same vector. Alongside, another vector was developed with chimeric cre recombinase gene cassette. Reciprocal crosses were performed between three single-copy T(0) plants with ASAL- lox-hpt-lox T-DNA and three single-copy T(0) plants with cre-bar T-DNA. Marker gene excisions were detected in T(1) hybrids through hygromycin sensitivity assay. Molecular analysis of T(1) plants exhibited 27.4% recombination efficiency. T(2) progenies of L03C04(1) hybrid parent showed 25% cre negative ASAL-expressing plants. Northern blot, western blot and ELISA showed significant level of ASAL expression in five marker-free T(2) progeny plants. In planta bioassay of GLH and BPH performed on these T(2) progenies exhibited radical reduction in survivability and fecundity compared with the untransformed control plants.
水稻是世界上主要的粮食作物,严重受到同翅目刺吸式害虫的影响。我们将大蒜叶片凝集素(ASAL)的编码序列导入水稻品种 IR64 中,以开发针对刺吸式昆虫的可持续抗性,同时利用 cre/lox 位点特异性重组系统消除了选择抗生素抗性标记基因潮霉素磷酸转移酶(hpt)。构建了一个表达载体,其中包含 ASAL 的编码序列,ASAL 是一种针对绿叶蝉(GLH,Nephotettix virescens)和褐飞虱(BPH,Nilaparvata lugens)的有效控制剂。选择标记(hpt)基因盒被克隆在同一载体的两个lox 位点内。同时,还开发了带有嵌合 cre 重组酶基因盒的另一个载体。在 ASAL-lox-hpt-lox T-DNA 和 cre-bar T-DNA 的三个单拷贝 T(0) 植物之间进行了相互杂交。通过潮霉素敏感性测定在 T(1)杂种中检测到标记基因的缺失。T(1) 植物的分子分析显示重组效率为 27.4%。L03C04(1)杂种亲本的 T(2)后代显示 25%的 cre 阴性 ASAL 表达植株。Northern blot、western blot 和 ELISA 显示在五个无标记的 T(2) 后代植物中有显著水平的 ASAL 表达。在这些 T(2) 后代植物上进行的 GLH 和 BPH 体内生物测定显示,与未转化的对照植物相比,生存能力和繁殖力有显著降低。