首页 | 本学科首页   官方微博 | 高级检索  
     检索      


Marker‐free,tissue‐specific expression of Cry1Ab as a safe transgenic strategy for insect resistance in rice plants
Authors:Yongbin Qi  Lei Chen  Xiuling He  Qingsheng Jin  Xiaoming Zhang  Zuhua He
Institution:1. Zhejiang Academy of Agricultural Science, Institute of Crops and Nuclear Technology Utilisation, Hangzhou, China;2. Biotechnology Institute, College of Agriculture and Biotechnology, Zhejiang University, Hangzhou, China;3. Zhejiang Academy of Agricultural Science, Serocultural Research Institute, Hangzhou, China;4. Institute of Plant Physiology and Ecology, Shanghai Institute for Biological Sciences, Chinese Academy of Sciences, Shanghai, China
Abstract:BACKGROUND: Rice is the major food resource for nearly half of the global population; however, insect infestation could severely affect the production of this staple food. To improve rice insect resistance and reduce the levels of Bt toxin released into the environment, the Cry1Ab gene was conjugated to the rice rbcS promoter to express Bt toxin in specific tissues of transgenic plants. RESULTS: Eight marker‐free, T2 lines were separated from the T0 cotransformants. Using RT‐PCR, high levels of Cry1Ab expression were detected in the leaf but not in the seed. The Cry1Ab protein level ranged from 1.66 to 3.31 µg g?1 in the leaves of four transgenic lines, but was barely detectable in their seeds by ELISA. Bioassays showed that the mortality rate of silkworm larvae feeding on mulberry leaves dipped in transgenic rice flour and pollen was less than that of the positive control (KMD), and that their average weight was higher than that of KMD, suggesting that the Cry1Ab protein was not expressed in the seed and pollen. CONCLUSION: The transgene conferred a high level of resistance to insects and biosafety to the rice plants, which could be directly used in rice breeding. Copyright © 2012 Society of Chemical Industry
Keywords:Cry1Ab gene  rbcS promoter  Bt toxin  co‐transformation  marker‐free  tissue‐specific expression
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号