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利用 RNAi 技术对大豆胞囊线虫背咽腺细胞中表达的先驱基因进行特征分析及组合 RNAi 的影响。

Characterisation by RNAi of pioneer genes expressed in the dorsal pharyngeal gland cell of Heterodera glycines and the effects of combinatorial RNAi.

机构信息

Centre for Plant Sciences, University of Leeds, Woodhouse Lane, Leeds, West Yorks LS2 9JT, UK.

出版信息

Int J Parasitol. 2008 Nov;38(13):1589-97. doi: 10.1016/j.ijpara.2008.05.003. Epub 2008 May 21.

Abstract

Changes in transcript abundance of 24 genes expressed in the dorsal pharyngeal gland cell of Heterodera glycines encoding for putative secretions of unknown function were monitored by quantitative PCR (qPCR) at 0, 2, 7, 14 and 21 days post-invasion (pi) of soybean plantlets. Five groups of temporal patterns (A, B1, B2, C and D) were defined for the 24 genes plus data for two previously studied genes expressed in the same cell. Group D (two genes) showed no significant increase between 0 and 2 days pi and were the least abundantly expressed at 7-21 days pi. Transcripts of group C (nine genes including one studied previously) increased in abundance from 0 to 2 days pi but were the second least expressed for 7-21 days pi. Groups A (three genes), B1 (seven genes) and B2 (five genes including one studied previously) were all abundant at 7-21 days pi. B1 and B2 were discriminated by their relative abundance at 0 and 2 days pi. RNA interference (RNAi) targeting two genes of group A and one each of B1 and B2 in nematodes prior to invasion resulted in phenotypic effects on total parasites per plant and sexual fate at 10 days pi. Phenotype penetrance was reduced for three genes showing such effects and one with a strong effect in earlier work when two genes rather than one were concurrently targeted for RNAi. One gene (dg13) was more abundantly expressed after combinatorial RNAi than for either control nematodes or when targeting singly by RNAi. This work reports the unexpected elevation in mRNA expression after combinatorial RNAi that requires understanding before combinatorial RNAi can be advanced for highly effective cyst nematode control via plant biotechnology.

摘要

在大豆幼苗被侵染后 0、2、7、14 和 21 天,通过定量 PCR(qPCR)监测了编码未知功能假定分泌蛋白的 24 个基因在背咽腺细胞中转录丰度的变化。将这 24 个基因加上在同一细胞中表达的两个先前研究过的基因的数据分为五组时间模式(A、B1、B2、C 和 D)。组 D(两个基因)在 0 到 2 天 pi 之间没有显著增加,在 7 到 21 天 pi 时表达量最少。组 C(包括一个先前研究过的基因在内的 9 个基因)的转录物丰度从 0 到 2 天 pi 增加,但在 7-21 天 pi 时表达量第二少。组 A(三个基因)、B1(七个基因)和 B2(包括一个先前研究过的基因在内的五个基因)在 7-21 天 pi 时都很丰富。B1 和 B2 可以通过它们在 0 和 2 天 pi 时的相对丰度来区分。在侵染前针对线虫中的组 A 的两个基因以及组 B1 和 B2 的每个基因进行 RNA 干扰(RNAi),导致侵染后 10 天每株植物的总寄生虫数量和性命运出现表型效应。当针对三个基因而非两个基因同时进行 RNAi 时,具有这种效应的三个基因的表型穿透率降低,而在早期工作中具有强烈效应的一个基因的穿透率降低。在组合 RNAi 后,一个基因(dg13)的表达丰度比对照线虫或单独进行 RNAi 时更高。这项工作报道了组合 RNAi 后出乎意料的 mRNA 表达升高,在可以通过植物生物技术实现高效控制胞囊线虫之前,需要对此进行理解。

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