Abstract:Based on the data from the International Agricultural Biotechnology Application Service Organization (ISAAA), the herbicide tolerance transgene events of 4 crops, including cotton (Gossypium hirsutum), soybean (Glycine max), canola (Brassica napus) and maize (Zea mays) were summarized. The aim is to provide important references for the development of herbicide tolerance transgenic crops in China. It was found that there were 328 herbicide tolerance transgene events by the end of 21 May 2017. These events are approved by the country concerned for direct consumption or as an additive or for cultivation. Herbicide tolerance transgene events of cotton, soybean, canola and maize were 39, 28, 32 and 201, respectively, accounted for 11.89%, 8.53%, 9.76% and 61.28% of the global herbicide tolerance transgenic events, respectively. Nineteen herbicide tolerance genes, which are derived from 16 kinds of organisms, involved in these herbicide tolerance events of these four crops. Seven out of 19 herbicide tolerance genes are derived from five plant genomes, including maize, arabidopsis (Arabidopsis thaliana), soybeans, tobacco (Nicotiana tabacum cv. Xanthi) and oats (Avena sativa), and the rest of 13 from microbial genomes. These 19 genes displayed tolerance to nine kinds of herbicides, which are glyphosate, glufosinate, imidazolinones, 2,4-dichlorophenoxy (2,4-D), isoxazolone, dicamba, sulfonylureas, mesotrione and bromoxynil. Singular herbicide tolerance events, multi herbicide tolerance events, stacked gene events (herbicide tolerance and other trait, such as insect resistance) were 25, 18 and 257, respectively, which accounted for 8.3%, 6% and 85.7% of the total herbicide tolerance events of four crops. These events were developed by eight companies, namely Syngenta, Monsanto Company, DuPont, Bayer CropScience, Dow AgroSciences LLC, BASF, Genective S.A. and the Stein Seed Farm Inc.(USA). Compared to the above international situation, the most of the herbicide tolerance events are glyphosate tolerance, mainly from microorganisms in China. Therefore several suggestions are put forward for developing herbicide tolerance events scientifically in China. Firstly, it is suggested to focus on the development of herbicide tolerance transgene events which should be from plants, because plants have abundant herbicide tolerance genes and herbicide metabolic genes. Secondly, it is recommended to develop glufosinate tolerance transgene events due to characteristics of glufosinate, such as broad spectrum, low toxicity and high activity, environmental compatibility, and excellent weed control effects. Thirdly, other herbicides tolerance transgene events, such as 2,4-D, mesotrione, bromoxynil and isoxazolones should be developed. The single herbicide tolerance crop would lead to the evolution of herbicide resistance weeds due to overreliance on a single herbicide or group of herbicides that share the same mechanism of action or of metabolism. Transgenic crops carried double herbicide tolerance and even more herbicide tolerance genes allow to rotations of herbicides with different modes of action and different metabolic pathways, which are more likely to delay the evolution of herbicide resistant weeds than using herbicide of the same mode of action. Finally, it is suggested to cultivate the event with stacked traits, which could improve the economic value and ecological benefit of the transgenic crops.
[1]向文胜, 肖振平, 赵长山.抗除草剂转基因作物[J].东北农业大学学报, 1998, 29(2):201-208[2]谢龙旭, 李云锋, 徐培林.根癌农杆菌介导的转基因棉花植株的草甘膦抗性[J].植物生理与分子生物学学报, 2004, 30(2):173-178[3]刘锡娟, 刘昱辉, 王志兴, 等.转-烯醇式丙酮酰莽草酸--磷酸合酶基因抗草甘膦烟草和棉花的获得[J].农业生物技术学报, 2007, 15(6):958-963[4]童旭宏.抗草甘膦棉花突变体R1098的选育及其抗性机理研究[D]. 浙江大学, 2011.(Tong X H. Anti-glyphosate cotton mutant R1098 breeding and its resistance mechanism [D]. Zhejiang University, 2011.)[5]冯艳.棉花转抗除草剂基因(Bar)植株的获得及其生理研究[D]. 河南农业大学, 2009.(Feng Y.Study on the Obtaining and Physiology of Cotton Herbicide Resistant Gene (Bar) Plants ; Journal of Henan Agricultural University, 2009.)[6]孙豹.GhEF1A8启动子克隆与功能分析及抗草甘膦转基因棉花研究[D]. 中国农业科学院, 2014.(Sun B. GhEF1A8 promoter cloning and functional analysis and anti-glyphosate transgenic cotton [D]. Chinese Academy of Agricultural Sciences, 2014.)[7]郭三堆, 孙豹, 孟志刚, 等.转抗虫、抗除草剂基因棉花分子育种[C]// 中国棉花学会2015年年会论文汇编. 2015.(Guo S D, Sun B, Meng Z G, etc .. Anti-insect, anti-herbicide gene cotton molecular breeding [C] / / China Cotton Society 2015 annual conference compilation.2015)[8]庞伟民, 靳茜, 王旭静, 等.陆地棉纤维优势表达基因GhRACK1克隆与序列分析[J].生物技术进展, 2015, 5(5):366-370[9]荣非, 王罡, 季静, 等.利用“微创刷”法获得抗草甘膦转基因大豆[J].大豆科学, 2015, 34(2):000217-223[10]邱丽娟, 郭勇, 常汝镇.2014年中国大豆基因资源发掘的主要进展[J].作物杂志, 2015, 1(1):1-5[11]韩强.抗虫及抗除草剂转基因大豆新品种的培育与鉴定[D]. 浙江大学, 2015.(Han Q. Insecticide and anti-herbicide transgenic soybean varieties of cultivation and identification [D]. Zhejiang University, 2015.)[12]钟蓉, 朱峰, 刘玉乐, 等.油菜的遗传转化及抗溴苯腈转基因油菜的获得[J].Journal of Integrative Plant Biology, 1997, 39(1):22-27[13]浦惠明, 戚存扣, 张洁夫, 等.甘蓝型油菜油蔬两用新品种宁杂号的选育[J].江苏农业学报, 2010, 26(6):1432-1434[14]胡茂龙, 浦惠明, 龙卫华, 等.一种甘蓝型油菜抗磺酰脲类除草剂基因及其应用:, CN 103266118 A[P]. 2013.Hu M L, Pu H M, Long W H, et al. A Brassica napus resistant sulfonylurea herbicide gene and its application: CN 103266118 A [P].2013.)[15]沈志成, 高建华.抗虫融合基因、融合蛋白质及其应用: CN, CN 102031266 A[P]. 2011.Shen Z C, Gao J H. Insect-resistant fusion gene, fusion protein and its application: CN, CN 102031266 A [P].2011.)[16]陈社员, 官春云, 刘忠松, 等.转基因抗除草剂油菜杂种优势利用系统研究I[J].转基因雄性不育系选育作物研究, 2015, 29(2):128-131[17]赖锦盛, 宋伟彬, 董永彬, 等.一种植物氮吸收和耐旱相关蛋白及其编码的基因和应用, CN 102666573 A[P]. 2012.(Lai J S, Song W B, Dong Y B, et al. A plant nitrogen absorption and drought tolerance related protein and its coding gene and its application, CN 102666573 A[P]. 2012.)[18]康越景, 郭明欣, 刘海利, 等.用于检测除草剂耐受性玉米植物DBN9898的核酸序列及其检测方法, CN104830846A[P]. 2015.(Kang Y J, Guo M X, Liu H L, et al. Methods for detecting nucleic acid sequences of herbicide tolerant maize plant DBN9898 and its detection method: CN104830846A [P]. 2015.)[19]孙越, 刘秀霞, 李丽莉, 等.抗亚洲玉米螟、抗草甘膦转基因玉米的培育[J].农业生物技术学报, 2015, 23(1):52-60[20]姜志军, 江颖, 徐摇光, 等.利用微滴数字方法快速分析转基因玉米中外源基因的拷贝数[J].生物技术进展, 2016, 6(4):288-294