National Key Laboratory of Crop Genetic Improvement, National Centre of Plant Gene Research, Huazhong Agricultural University, Wuhan, China.
College of Plant Science and Technology, Huazhong Agricultural University, Wuhan, China.
Pest Manag Sci. 2020 Sep;76(9):3177-3187. doi: 10.1002/ps.5872. Epub 2020 May 10.
Promoters play a key role in driving insect-resistant genes during breeding of transgenic plants. In current transgenic procedures for breeding rice resistance to striped stem borer (Chilo suppressalis Walker, SSB), the constitutive promoter is used to drive the insect-resistant gene. To reduce the burden of constitutive promoters on plant growth, isolation and identification of insect-inducible promoters are particularly important. However, few promoters are induced specifically by insect feeding.
We found rice hydroperoxide lyase gene (OsHPL2) (LOC_Os02g12680) was upregulated after feeding by SSB. We subsequently cloned the promoter of OsHPL2 and analysed its expression pattern using the β-glucuronidase (GUS) reporter gene. Histochemical assays and quantitative analyses of GUS activity confirmed that P :GUS was activated by SSB, but did not respond to brown planthopper (Nilaparvata lugens Stål, BPH) infestation, mechanical wounding or phytohormone treatments. A series of 5' truncated assays were conducted and three positive regulatory regions (-1452 to -1213, -903 to -624, and -376 to -176) induced by SSB infestation were identified. P2R123-min 35S and P2TR2-min 35S promoters linked with cry1C of transgenic plants showed the highest levels of Cry1C protein expression and SSB larval mortality.
We identified an SSB-inducible promoter and three positive internal regions. Transgenic rice plants with the OsHPL2 promoter and its positive regions driving cry1C exhibited the expected larvicidal effect on SSB. Our study is the first report of an SSB-inducible promoter that could be used as a potential resource for breeding insect-resistant transgenic crops. © 2020 Society of Chemical Industry.
启动子在培育转基因植物的过程中对驱动抗虫基因起着关键作用。在当前培育抗条纹叶枯病水稻的转基因过程中,使用组成型启动子驱动抗虫基因。为了减轻组成型启动子对植物生长的负担,分离和鉴定昆虫诱导型启动子尤为重要。然而,很少有启动子能被昆虫取食特异性诱导。
我们发现水稻过氧化氢酶基因(OsHPL2)(LOC_Os02g12680)在被 SSB 取食后上调。我们随后克隆了 OsHPL2 的启动子,并利用β-葡萄糖醛酸酶(GUS)报告基因分析了其表达模式。组织化学分析和 GUS 活性的定量分析证实,P :GUS 被 SSB 激活,但对褐飞虱(Nilaparvata lugens Stål,BPH)取食、机械损伤或植物激素处理没有反应。进行了一系列 5'截短分析,鉴定了三个受 SSB 取食诱导的正调控区(-1452 至-1213、-903 至-624 和-376 至-176)。与 cry1C 连接的 P2R123-min 35S 和 P2TR2-min 35S 启动子在转cry1C 植物中显示出最高水平的 Cry1C 蛋白表达和 SSB 幼虫死亡率。
我们鉴定了一个 SSB 诱导型启动子和三个正的内部区域。含有 OsHPL2 启动子及其正区域驱动 cry1C 的转基因水稻表现出对 SSB 的预期杀虫效果。我们的研究首次报道了一个 SSB 诱导型启动子,可作为培育抗虫转基因作物的潜在资源。© 2020 化学工业协会。