Shabbir Muhammad Zeeshan, Zhang Tiantao, Wang Zhenying, He Kanglai
State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, China.
Front Physiol. 2019 Feb 1;10:27. doi: 10.3389/fphys.2019.00027. eCollection 2019.
Asian corn borer (ACB), can develop resistance to transgenic (Bt) maize expressing Cry1Ah-toxin. However, the mechanisms that regulate the resistance of ACB to Cry1Ah-toxin are unknown. In order to understand the molecular basis of the Cry1Ah-toxin resistance in ACB, "omics" analyses were performed to examine the difference between Cry1Ah-resistant (ACB-AhR) and susceptible (ACB-BtS) strains of ACB at both transcriptional and translational levels. A total of 7,007 differentially expressed genes (DEGs) and 182 differentially expressed proteins (DEPs) were identified between ACB-AhR and ACB-BtS and 90 genes had simultaneous transcription and translation profiles. Down-regulated genes associated with Cry1Ah resistance included aminopeptidase N, ABCC3, DIMBOA-induced cytochrome P450, alkaline phosphatase, glutathione -transferase, cadherin-like protein, and V-ATPase. Whereas, anti-stress genes, such as heat shock protein 70 and carboxylesterase were up-regulated in ACB-AhR, displaying that a higher proportion of genes/proteins related to resistance was down-regulated compared to up-regulated. The Kyoto encyclopedia of genes and genomes (KEGG) analysis mapped 578 and 29 DEGs and DEPs, to 27 and 10 pathways, respectively ( < 0.05). Furthermore, real-time quantitative (qRT-PCR) results based on relative expression levels of randomly selected genes confirmed the "omics" response. Despite the previous studies, this is the first combination of a study using RNA-Seq and iTRAQ approaches on Cry1Ah-toxin binding, which led to the identification of longer length of unigenes in ACB. The DEGs and DEPs results are valuable for further clarifying Cry1Ah-mediated resistance.
亚洲玉米螟(ACB)能够对表达Cry1Ah毒素的转基因玉米产生抗性。然而,调控ACB对Cry1Ah毒素抗性的机制尚不清楚。为了了解ACB对Cry1Ah毒素抗性的分子基础,进行了“组学”分析,以检测ACB的Cry1Ah抗性(ACB-AhR)品系和敏感(ACB-BtS)品系在转录和翻译水平上的差异。在ACB-AhR和ACB-BtS之间共鉴定出7007个差异表达基因(DEG)和182个差异表达蛋白(DEP),其中90个基因具有同步的转录和翻译谱。与Cry1Ah抗性相关的下调基因包括氨肽酶N、ABCC3、DIMBOA诱导的细胞色素P450、碱性磷酸酶、谷胱甘肽-S-转移酶、类钙黏蛋白和V-ATP酶。而抗应激基因,如热休克蛋白70和羧酸酯酶在ACB-AhR中上调,表明与抗性相关的基因/蛋白下调的比例高于上调的比例。京都基因与基因组百科全书(KEGG)分析分别将578个DEG和29个DEP映射到27条和10条通路(<0.05)。此外,基于随机选择基因的相对表达水平的实时定量(qRT-PCR)结果证实了“组学”响应。尽管有先前的研究,但这是首次将RNA-Seq和iTRAQ方法结合用于Cry1Ah毒素结合的研究,该研究导致在ACB中鉴定出更长的单基因长度。DEG和DEP结果对于进一步阐明Cry1Ah介导的抗性具有重要价值。