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利用叶盘介导的 dsRNA 系统传递筛选食 RNAi 致死基因在二斑叶螨中的应用。

Screening of lethal genes for feeding RNAi by leaf disc-mediated systematic delivery of dsRNA in Tetranychus urticae.

机构信息

Department of Agricultural Biotechnology, Seoul National University, Seoul 151-742, Republic of Korea.

出版信息

Pestic Biochem Physiol. 2013 Jan;105(1):69-75. doi: 10.1016/j.pestbp.2012.12.001. Epub 2012 Dec 19.

Abstract

To identify genes that kill Tetranychus urticae when knocked down via RNA interference (RNAi), several lethal genes were screened by the systemic delivery of dsRNA via leaf disc feeding. Four candidate genes (β subunit of coatomer protein complex, T-COPB2; M1 metalloprotease, T-M1MP; Ribosomal protein S4, T-RPS4; A subunit of V-ATPase, T-VATPase) and a control gene (EGFP) were tested for RNAi. All dsRNAs that permeated the leaf disc (ca. 15-mm diameter) were detected at 12h post-treatment, indicating that dsRNA could move through vascular tissues. To evaluate RNAi toxicity, mortalities were assessed for 120h following treatment with dsRNA. Treatment with T-COPB2, T-M1MP, T-RPS4 and T-VATPase dsRNAs caused 65.4%, 15.9%, 36.1% and 21.1% mortalities at 120h post-treatment, respectively. Reduction of all target gene transcripts following dsRNA treatment was confirmed by quantitative PCR, demonstrating that dsRNA feeding-based RNAi could indeed kill T. urticae. In summary, dsRNA delivery via leaf disc is an effective system to screen for lethal genes. Furthermore, some genes, such as T-COPB2, T-M1MP, T-RPS4 and T-VATPase, can be used to establish an RNAi-based control system against T. urticae.

摘要

为了鉴定通过 RNA 干扰(RNAi)敲低时杀死桃蚜的基因,通过叶盘喂食系统递送来筛选了几个致死基因。测试了四个候选基因(衣壳蛋白复合物β亚基,T-COPB2;M1 金属蛋白酶,T-M1MP;核糖体蛋白 S4,T-RPS4;V-ATP 酶 A 亚基,T-VATPase)和一个对照基因(EGFP)的 RNAi。处理后 12 小时检测到渗透叶盘(约 15mm 直径)的所有 dsRNA,表明 dsRNA 可以通过血管组织移动。为了评估 RNAi 毒性,在处理 dsRNA 后 120 小时评估死亡率。用 T-COPB2、T-M1MP、T-RPS4 和 T-VATPase dsRNA 处理分别在 120 小时后导致 65.4%、15.9%、36.1%和 21.1%的死亡率。通过定量 PCR 证实了 dsRNA 处理后所有靶基因转录本的减少,表明 dsRNA 喂食基 RNAi 确实可以杀死桃蚜。综上所述,通过叶盘递送 dsRNA 是筛选致死基因的有效系统。此外,一些基因,如 T-COPB2、T-M1MP、T-RPS4 和 T-VATPase,可用于建立针对桃蚜的 RNAi 控制体系。

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