Centro de Recursos Naturales Renovables de la Zona Semiárida (CERZOS) - CONICET, Camino de La Carrindanga Km 7, 8000 Bahía Blanca, Argentina.
Departamento de Agronomía, Universidad Nacional del Sur, San Andrés 800, 8000 Bahía Blanca, Argentina.
Microbiol Res. 2015 Aug;177:53-66. doi: 10.1016/j.micres.2015.04.012. Epub 2015 May 28.
The wheat recombinant chromosome inbred line LDN(Dic-3A)10, obtained through introgression of a Triticum dicoccoides disomic chromosome 3A fragment into Triticum turgidum spp. durum var. Langdon, is resistant to fusarium head blight (FHB) caused by Fusarium graminearum. To identify genes involved in FHB resistance, we used a cDNA-AFLP approach to compare gene expression between LDN(Dic-3A)10 and the susceptible parental line LDN at different time points post-inoculation. In total, 85 out of the ∼ 500 transcript-derived fragments (TDFs) were found to be differentially expressed: 36 and 19% were upregulated in LDN(Dic-3A)10 and LDN, respectively, whereas 45% were induced in both genotypes. Several of the cloned TDFs showed similarity to proteins involved in specific recognition of plant pathogens or associated with early responses to infection. Some TDFs specific to the inoculation response did not show similarity to characterized proteins. The availability of T. aestivum genome sequences allowed the in silico mapping of 28 TDFs and the acquirement of the corresponding gene sequences and, in some cases, their regulatory regions. Analysis of promoter regions revealed the potential existence of shared transcription regulation mechanisms. For instance, three TDF-associated genes contained binding sites for WRKY transcription factors, which have been implicated in the regulation of genes associated with pathogen defense, and three for abscisic acid-responsive element (ABRE). Collectively, our results revealed specific pathogen recognition in the interactions of LDN and LDN(Dic-3A)10 with F. graminearum. Such recognition leads to changes in the expression of several transcripts, attributable to the presence of the wheat QTL Qfhs.ndsu-3AS.
通过将一个普通小麦 3A 染色体 3A 片段导入到硬粒小麦品种 Langdon 中,获得了一个小麦重组近交系 LDN(Dic-3A)10,该近交系对禾谷镰刀菌引起的小麦赤霉病具有抗性。为了鉴定与赤霉病抗性相关的基因,我们使用 cDNA-AFLP 方法比较了接种后不同时间点 LDN(Dic-3A)10 和易感亲本系 LDN 之间的基因表达。总共发现了约 500 个转录衍生片段(TDFs)中的 85 个差异表达:36%和 19%分别在 LDN(Dic-3A)10 和 LDN 中上调,而 45%在两种基因型中均被诱导。克隆的一些 TDFs 与参与植物病原体特异性识别或与感染早期反应相关的蛋白具有相似性。一些与接种反应特异性相关的 TDFs 与已鉴定的蛋白没有相似性。由于有了小麦基因组序列,我们可以对 28 个 TDFs 进行计算机定位,并获得相应的基因序列,在某些情况下,还可以获得其调控区。启动子区域分析表明,可能存在共享的转录调控机制。例如,三个与 TDF 相关的基因含有 WRKY 转录因子的结合位点,WRKY 转录因子已被证明与与病原体防御相关的基因的调控有关,还有三个基因含有脱落酸应答元件(ABRE)。总的来说,我们的研究结果揭示了 LDN 和 LDN(Dic-3A)10 与禾谷镰刀菌相互作用中特定的病原体识别。这种识别导致了几个转录物表达的变化,这归因于小麦 QTL Qfhs.ndsu-3AS 的存在。