Szakasits Dagmar, Heinen Petra, Wieczorek Krzysztof, Hofmann Julia, Wagner Florian, Kreil David P, Sykacek Peter, Grundler Florian M W, Bohlmann Holger
Department of Applied Plant Sciences and Plant Biotechnology, Institute of Plant Protection, University of Natural Resources and Applied Life Sciences, Vienna, Austria.
Plant J. 2009 Mar;57(5):771-84. doi: 10.1111/j.1365-313X.2008.03727.x. Epub 2008 Oct 29.
Arabidopsis thaliana is a host for the sugar beet cyst nematode Heterodera schachtii. Juvenile nematodes invade the roots and induce the development of a syncytium, which functions as a feeding site for the nematode. Here, we report on the transcriptome of syncytia induced in the roots of Arabidopsis. Microaspiration was employed to harvest pure syncytium material, which was then used to prepare RNA for hybridization to Affymetrix GeneChips. Initial data analysis showed that the gene expression in syncytia at 5 and 15 days post-infection did not differ greatly, and so both time points were compared together with control roots. Out of a total of 21 138 genes, 18.4% (3893) had a higher expression level and 15.8% (3338) had a lower expression level in syncytia, as compared with control roots, using a multiple-testing corrected false discovery rate of below 5%. A gene ontology (GO) analysis of up- and downregulated genes showed that categories related to high metabolic activity were preferentially upregulated. A principal component analysis was applied to compare the transcriptome of syncytia with the transcriptome of different Arabidopsis organs (obtained by the AtGenExpress project), and with specific root tissues. This analysis revealed that syncytia are transcriptionally clearly different from roots (and all other organs), as well as from other root tissues.
拟南芥是甜菜孢囊线虫(Heterodera schachtii)的宿主。线虫幼虫侵入根部并诱导多核细胞的形成,多核细胞作为线虫的取食位点。在此,我们报道了拟南芥根中诱导形成的多核细胞的转录组。采用微量吸出法获取纯净的多核细胞材料,然后用其制备RNA用于与Affymetrix基因芯片杂交。初步数据分析表明,感染后5天和15天的多核细胞中的基因表达差异不大,因此将这两个时间点的数据与对照根一起进行比较。在总共21138个基因中,与对照根相比,使用多重检验校正的错误发现率低于5%时,有18.4%(3893个)基因在多核细胞中的表达水平较高,15.8%(3338个)基因在多核细胞中的表达水平较低。对上调和下调基因进行的基因本体论(GO)分析表明,与高代谢活性相关的类别优先上调。应用主成分分析将多核细胞的转录组与不同拟南芥器官(通过AtGenExpress项目获得)以及特定根组织的转录组进行比较。该分析表明,多核细胞在转录水平上与根(以及所有其他器官)以及其他根组织明显不同。