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首页> 外文期刊>Environmental and experimental botany >Transcriptome wide identification and characterization of NO-responsive WRKY transcription factors in Arabidopsis thaliana L.
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Transcriptome wide identification and characterization of NO-responsive WRKY transcription factors in Arabidopsis thaliana L.

机译:转录组拟南芥L的无响应腕骨转录因子的宽鉴定与表征。

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摘要

WRKY transcription factors are important plant-specific regulatory genes characterized by one or two conserved WRKY domain(s) usually followed by a zinc-finger motif. In this study using Arabidopsis thaliana, the RNA-Seq based transcriptomic analysis showed differential expression of 33 genes encoding WRKY TFs in response to the nitric oxide (NO) donor S-Nitrosocysteine (CySNO). Interestingly, 93.9% of these TFs were up-regulated with at least 2-fold change, suggesting their putative involvement in NO mediated gene regulation. GO- analysis of all the 33 transcriptomic elements showed their putative involvement in biological processes such as abiotic stress tolerance and defense against fungal pathogens (89.39 fold enrichment). Analysis of the NO-responsive AtWRKY TFs promoter region revealed the presence of the cis-acting elements such as ABRE, EIRE, ERE, and MBS involved in osmotic stress response, maximal elicitor-mediated activation, and drought-stress regulation. The analysis of NO-responsive AtWRKY TF motifs and their comparison with rice, soybean, and tomato orthologs suggested that members of the WRKY family belonging to the same group shared similar motifs and phylogenetic tree suggested that these TFs were highly conserved. Validation of transcriptomic data through quantitative real time-PCR showed a high correlation coefficient (0.85) indicating the high reliability and similarity of both types of analysis. Comparison of the NO-responsive and non-responsive WRKYs showed the presence of tyrosine (T) and cysteine (C) residues at a distance of 7 residues from the WRKYGQK motif which may serve as potential targets for modification by NO via tyrosine nitration and S-nitrosylation. We also validated the response of WRKYs through in vivo analysis using atwrky62 loss of function mutant and the results indicated a negative role of AtWRKY62 in plant growth. Furthermore, atwrky62 showed significantly less SNO contents compared to wild type plants indicating putative role of AtWRKY62 in NO metabolism.
机译:Wrky转录因子是一种重要的植物特异性调节基因,其特征是一种或两个保守的腕面,通常是锌手指基序。在该研究中使用rapidopsis thaliana,基于RNA-SEQ的转录组分析显示了响应于一氧化氮(NO)供体S-氮细胞(Cysno)编码Wrky TFS的33基因的差异表达。有趣的是,这些TF的93.9%上调,变化至少为2倍,表明其推定的涉及没有介导的基因调控。所有33个转录组分元素的去分析表明,他们推定了对真菌病原体(89.39倍富集)的非生物胁迫耐受和防御等生物过程的推定参与。 No-Encoorive ATWRKY TFS启动子区域的分析揭示了CIS作用元件的存在,例如参与渗透应激反应,最大引导介导的活化和干旱应激调节的MB。对禁区ATWRKY TF主题的分析及其与水稻,大豆和番茄灭绝的比较表明,属于同一组的腕骨家族的成员共享类似的主题和系统发育树,表明这些TFS高度保守。通过定量实时PCR验证转录组数据显示出高相关系数(0.85),表明两种类型的分析的高可靠性和相似性。无响应性和非响应性的禁区和无响应器的比较显示酪氨酸(T)和半胱氨酸(C)残留物,其来自Wrkygqk基序的7个残基的距离,其可以作为通过酪氨酸硝化和s的潜在靶标进行修饰的靶标的靶标 - 硝基化。我们还通过ATWRKY62失去功能突变体验证了WRKYS通过体内分析的响应,结果表明ATWRKY62在植物生长中的负面作用。此外,与野生型植物相比,ATWRKY62显着较少,表明ATWRKY62没有代谢的推定作用。

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