首页> 外文期刊>Planta: An International Journal of Plant Biology >Transgenic rice expressing Allium sativum leaf lectin with enhanced resistance against sap-sucking insect pests
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Transgenic rice expressing Allium sativum leaf lectin with enhanced resistance against sap-sucking insect pests

机译:转基因水稻表达大蒜叶片凝集素,增强对树液吸虫的抗性

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Mannose binding Allium sativum leaf agglutinin (ASAL) has been shown to be antifeedant and insecticidal against sap-sucking insects. In the present investigation, ASAL coding sequence was expressed under the control of CaMV35S promoter in a chimeric gene cassette containing plant selection marker, hpt and gusA reporter gene of pCAMBIA1301 binary vector in an elite indica rice cv. IR64. Many fertile transgenic plants were generated using scutellar calli as initial explants through Agrobacterium-mediated transformation technology. GUS activity was observed in selected calli and in mature plants. Transformation frequency was calculated to be approximately 12.1%+/-0.351 (mean +/- SE). Southern blot analyses revealed the integration of ASAL gene into rice genome with a predominant single copy insertion. Transgene localization was detected on chromosomes of transformed plants using PRINS and C-PRINS techniques. Northern and western blot analyses determined the expression of transgene in transformed lines. ELISA analyses estimated ASAL expression up to 0.72 and 0.67% of total soluble protein in T0 and T1 plants, respectively. Survival and fecundity of brown planthopper and green leafhopper were reduced to 36% (P < 0.01), 32% (P < 0.05) and 40.5, 29.5% (P < 0.001), respectively, when tested on selected plants in comparison to control plants. Specific binding of expressed ASAL to receptor proteins of insect gut was analysed. Analysis of T1 progenies confirmed the inheritance of the transgenes. Thus, ASAL promises to be a potential component in insect resistance rice breeding programme.
机译:甘露糖结合大蒜叶片的叶凝集素(ASAL)已被证明是抗饲料和杀虫剂,对吸树液的昆虫。在本研究中,ASAL编码序列在CaMV35S启动子的控制下在嵌合基因盒中表达,该嵌合基因盒包含植物plant选标记,hpt和pCAMBIA1301二元载体的gusA报告基因,在lite稻中表达。 IR64。通过农杆菌介导的转化技术,使用小cut愈伤组织作为初始外植体产生了许多可育的转基因植物。在选定的愈伤组织和成熟植物中观察到GUS活性。计算出的转化频率约为12.1%+ /-0.351(平均+/- SE)。 Southern印迹分析揭示了具有主要单拷贝插入的ASAL基因整合到水稻基因组中。使用PRINS和C-PRINS技术在转化植物的染色体上检测到转基因定位。 Northern和Western印迹分析确定了转基因在转化品系中的表达。 ELISA分析估计AS0在T0和T1植物中的表达分别高达总可溶性蛋白的0.72和0.67%。与对照植物相比,在选定的植物上测试时,褐飞虱和绿叶蝉的存活率和繁殖力分别降低至36%(P <0.01),32%(P <0.05)和40.5、29.5%(P <0.001)。 。分析了表达的ASAL与昆虫肠道受体蛋白的特异性结合。对T1子代的分析证实了转基因的遗传。因此,ASAL有望成为抗虫水稻育种计划的潜在组成部分。

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