Genetic Stability and Disease Resistance Analysis of Hrpzpsta Gene in Transgenic Soybean Lines

Miao Yu, Peiwu Wang, Yang Song, Yong-Qi Feng, J. Qu, Jie Rong, Mo Zhang, Zhuo Zhang
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Abstract

This experiment was carried out to evaluate genetic stability and disease resistance in transformed soybean lines with hrpZpsta gene using PCR analysis, southern blotting, real-time quantitative PCR (qRT-PCR) and to analyze the resistance against Phytophthora sojae (P. sojae) and Cercospora sojina (C. sojina) after inoculation. The results obtained using PCR and southern blotting analytical methods showed that exogenous gene functional elements were stably inherited in transgenic soybean and hrpZpsta gene was successfully integrated into the soybean genome in a single copy. Results at high-generation (T7, T8) transgenic lines of hrpZpsta revealed that their relative expression of hrpZpsta gene was the highest in leaves followed by roots, and much lower in stems, flowers, and seeds. Activity change rates of peroxidase (POD), polyphenol oxidase (PPO) and phenylalanine ammonia lyase (PAL) showed that transgenic lines significantly enhanced receptor species. The resistance of transgenic strains T7 and T8 generations against P. sojae was significantly increased with artificial inoculation methods, and the resistance against C. sojina was increased from susceptibility to the level of resistance. Under natural conditions in the field, the response of T8 transgenic lines to C. sojina reached disease resistance level. There were no significant differences in transgenic lines and recipient variety in maturing stage, leaf shape, flower color, plant height, 100-grain weight and quality content, and the two years average yield of plots increased to 11.59% and 8.19%, which significantly higher than recipient cultivar. The current results provide data support for the release of transgenic lines.
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转基因大豆品系Hrpzpsta基因的遗传稳定性及抗病性分析
本试验采用PCR、southern blotting、实时荧光定量PCR (qRT-PCR)技术,对转染hrpZpsta基因的大豆品系的遗传稳定性和抗病性进行了评价,并对接种后的大豆疫霉(P. sojae)和大豆Cercospora (C. sojina)进行了抗性分析。PCR和southern blotting分析结果表明,外源基因功能元件在转基因大豆中稳定遗传,hrpZpsta基因成功单拷贝整合到大豆基因组中。结果表明,高代(T7、T8)转基因植株叶片中hrpZpsta基因的相对表达量最高,其次为根,茎、花和种子中相对表达量较低。过氧化物酶(POD)、多酚氧化酶(PPO)和苯丙氨酸解氨酶(PAL)的活性变化率显示转基因系显著增强了受体种类。人工接种转基因菌株T7和T8对大豆弧菌的抗性显著提高,对大豆弧菌的抗性由易感水平提高到抗性水平。在田间自然条件下,T8转基因品系对粟粉虫的反应达到抗病水平。转基因品系与受体品种在成熟期、叶形、花色、株高、百粒重、品质含量等方面均无显著差异,地块2年平均产量分别达到11.59%和8.19%,显著高于受体品种。目前的结果为转基因品系的释放提供了数据支持。
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