Department of Plant Protection, Institute of Vegetables and Flowers, Chinese Academy of Agricultural Sciences, Beijing 100081, China.
Department of Entomology, Institute of Plant Protection, Hunan Academy of Agricultural Sciences, Changsha 410125, China.
Pestic Biochem Physiol. 2022 Mar;182:105053. doi: 10.1016/j.pestbp.2022.105053. Epub 2022 Feb 7.
Deciphering the molecular mechanisms of insect resistance to Bacillus thuringiensis (Bt) based biotechnology products including Bt sprays and Bt crops is critical for the long-term application of Bt technology. Previously, we established that down-regulation of the ABC transporter gene PxABCG1, trans-regulated by the MAPK signaling pathway, contributed to high-level resistance to Bt Cry1Ac toxin in diamondback moth, Plutella xylostella (L.). However, the underlying transcriptional regulatory mechanism was unknown. Herein, we identified putative binding sites (PBSs) of the transcription factor (TF) POUM1 in the PxABCG1 promoter and used a dual-luciferase reporter assay (DLRA) and yeast one-hybrid (Y1H) assay to reveal that POUM1 activates PxABCG1 via interaction with one of these sites. The expression of POUM1 was significantly decreased in the midgut tissue of Cry1Ac-resistant P. xylostella strains compared to a Cry1Ac-susceptible P. xylostella strain. Silencing of POUM1 expression resulted in reduced expression of the PxABCG1 gene and an increase in larval tolerance to Bt Cry1Ac toxin in the Cry1Ac-susceptible P. xylostella strain. Furthermore, silencing of PxMAP4K4 expression increased the expression of both POUM1 and PxABCG1 genes in the Cry1Ac-resistant P. xylostella strain. These results indicate that the POUM1 induces PxABCG1 expression, while the activated MAPK cascade represses PxABCG1 expression thus reducing Cry1Ac susceptibility in P. xylostella. This result deepens our understanding of the transcriptional regulatory mechanism of midgut Cry receptor genes and the molecular basis of the evolution of Bt resistance in insects.
解析昆虫对苏云金芽孢杆菌(Bt)基于生物技术产品,包括 Bt 喷雾和 Bt 作物的抗性的分子机制,对于 Bt 技术的长期应用至关重要。此前,我们已经确定,ABC 转运蛋白基因 PxABCG1 的下调,受丝裂原活化蛋白激酶(MAPK)信号通路的反式调节,有助于小菜蛾对 Bt Cry1Ac 毒素的高水平抗性。然而,其潜在的转录调控机制尚不清楚。在此,我们在 PxABCG1 启动子中鉴定出转录因子(TF)POUM1 的假定结合位点(PBS),并使用双荧光素酶报告基因检测(DLRA)和酵母单杂交(Y1H)测定来揭示 POUM1 通过与其中一个位点的相互作用来激活 PxABCG1。与 Cry1Ac 敏感的小菜蛾菌株相比,Cry1Ac 抗性小菜蛾菌株的中肠组织中 POUM1 的表达显著降低。沉默 POUM1 的表达导致 Cry1Ac 敏感的小菜蛾菌株中 PxABCG1 基因的表达减少,并且对 Bt Cry1Ac 毒素的幼虫耐受性增加。此外,沉默 PxMAP4K4 的表达增加了 Cry1Ac 抗性小菜蛾菌株中 POUM1 和 PxABCG1 基因的表达。这些结果表明,POUM1 诱导 PxABCG1 的表达,而激活的 MAPK 级联反应抑制 PxABCG1 的表达,从而降低小菜蛾对 Cry1Ac 的敏感性。这一结果加深了我们对中肠 Cry 受体基因转录调控机制的理解,以及昆虫对 Bt 抗性的分子基础的认识。