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[Xa21基因在转基因水稻CX8621中的整合与表达]

[Integration and expression of Xa21 in transgenic rice CX8621].

作者信息

Gao Lifen, Liu Pengcheng, Xia Zhihui, Zhao Jiying, Shi Jianan, Jiang Guanghuai, Liu Guozhen, Zhai Wenxue

机构信息

Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China.

Institute for System Biology, Jianghan University, Wuhan 430056, Hubei, China.

出版信息

Sheng Wu Gong Cheng Xue Bao. 2016 Sep 25;32(9):1255-1263. doi: 10.13345/j.cjb.150549.

Abstract

Agrobacterium tumefaciens-mediated transformation system has been widely applied. However, the function of target gene is affected by multiple factors. With this system, we obtained a transgenic rice line CX8621 carrying the bacterial blight resistance gene Xa21. In previous work, we have confirmed that it was selectable maker-free and vector backbone-free. And after 16 generations of breeding, it still maintained perfect resistance to bacterial blight disease. On this basis, we analyzed the integration and expression of Xa21 in CX8621 at the present study. First, based on the border sequences of plasmid pBXa21 and Xa21, we designed nested primers and assured the integrity of Xa21 in CX8621. Second, we cloned the flanking sequences and located Xa21 on chromosome 2 using improved Tail-PCR. Then we analyzed the expression pattern of Xa21 in several tissues and at different developmental stages by RT-PCR. The results show that Xa21 can be stably expressed in CX8621, agreeing well with the disease resistance response as reported previously. In addition, we detected the protein levels of XA21 in CX8621 with antibody of natural XA21 protein. Surprisingly, no XA21 protein was detected in the seeds of CX8621. Thus, the integration and expression analysis of Xa21 in CX8621 provided a part of scientific evidences for the safety assessment of genetically modified rice.

摘要

根癌农杆菌介导的转化系统已得到广泛应用。然而,靶基因的功能受多种因素影响。利用该系统,我们获得了携带白叶枯病抗性基因Xa21的转基因水稻品系CX8621。在先前的工作中,我们已证实它无选择标记且无载体骨架。经过16代繁殖后,它对白叶枯病仍保持完美抗性。在此基础上,本研究对CX8621中Xa21的整合与表达进行了分析。首先,基于质粒pBXa21和Xa21的边界序列,设计巢式引物并确定CX8621中Xa21的完整性。其次,克隆侧翼序列并利用改进的Tail-PCR将Xa21定位到第2号染色体上。然后通过RT-PCR分析Xa21在几个组织和不同发育阶段的表达模式。结果表明,Xa21在CX8621中能稳定表达,与先前报道的抗病反应一致。此外,我们用天然XA21蛋白抗体检测了CX8621中XA21的蛋白水平。令人惊讶的是,在CX8621的种子中未检测到XA21蛋白。因此,对CX8621中Xa21的整合与表达分析为转基因水稻的安全性评估提供了部分科学依据。

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