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首页> 外文期刊>Plant Molecular Biology >Analysis of rice genes induced by striped stemborer (Chilo suppressalis) attack identified a promoter fragment highly specifically responsive to insect feeding
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Analysis of rice genes induced by striped stemborer (Chilo suppressalis) attack identified a promoter fragment highly specifically responsive to insect feeding

机译:通过对条带化stem虫攻击而诱导的水稻基因的分析确定了对昆虫摄食具有高度特异性反应的启动子片段

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摘要

The objective of this study was to identify rice gene promoters that are specifically induced by feeding of the striped stemborer (Chilo suppressalis). Two PCR-selected cDNA subtractive libraries were constructed from the rice variety Minghui 63. Up- and down-regulated cDNAs induced by C. suppressalis feeding were arrayed on nylon membranes. After array hybridization and Northern blot analysis, a cDNA (B1-A04) encoding a putative subtilisin/chymotrypsin inhibitor was found to be rapidly and highly induced by C. suppressalis feeding, compared with mechanical wounding. The putative promoter region, spanning from -1,569 to +446 relative to the transcriptional initiation site was isolated, fused to the GUS gene (beta-glucuronidase reporter gene) and introduced by Agrobacterium-mediated transformation to rice. In non-infested plants, the GUS activity driven by this promoter fragment was detected in culms and panicles, but not in leaves and sheaths. At 6 h after insect feeding, GUS activity was significantly induced in sheaths and culms, but not in leaves. GUS activity and native B1-A04 gene were not induced by JA and ABA treatment. A serial deletion analysis revealed two regions (-1,569 to -1,166 and -1,166 to -582) that negatively regulate the gene expression in sheaths of non-infested plants but not in insect-infested plants. An electrophoretic mobility shift assay (EMSA) identified 7 DNA fragments with various binding activities with nuclear proteins from mechanically wounded, insect-infested and untreated plants, and their possible roles in gene regulation were speculated. This promoter fragment should have utility in development of insect resistant transgenic crops.
机译:这项研究的目的是鉴定水稻基因启动子,该基因是通过饲喂条带化stem(Chilo hypoalis)而特异性诱导的。从水稻品种Minghui 63中构建了两个PCR选择的cDNA消减文库。通过抑制suppress虫的进食诱导的上,下调cDNA排列在尼龙膜上。经过阵列杂交和Northern印迹分析后,发现编码的枯草杆菌蛋白酶/胰凝乳蛋白酶抑制剂的cDNA(B1-A04)与机械损伤相比,可通过抑制隐孢子虫快速而高度地诱导。分离出相对于转录起始位点介于-1,569至+446之间的推定启动子区域,与GUS基因(β-葡萄糖醛酸苷酶报道基因)融合,并通过农杆菌介导的方法导入水稻。在未受侵染的植物中,由该启动子片段驱动的GUS活性在茎和穗中检测到,但在叶和鞘中未检测到。昆虫喂食后6小时,鞘和茎中明显诱导了GUS活性,但叶片中未诱导。 JA和ABA处理未诱导GUS活性和天然B1-A04基因。序列缺失分析揭示了两个区域(-1,569至-1,166和-1,166至-582),这些区域对未受侵染的植物的鞘中的基因表达有负调控,但对昆虫受侵染的植物却没有。电泳迁移率迁移分析(EMSA)鉴定了7种具有与机械伤害,虫害和未处理植物的核蛋白具有各种结合活性的DNA片段,并推测了它们在基因调控中的可能作用。该启动子片段应在抗虫转基因作物的开发中具有实用性。

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