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首页> 外文期刊>Scientific reports. >Analysis of TabZIP15 transcription factor from Trichoderma asperellum ACCC30536 and its function under pathogenic toxin stress
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Analysis of TabZIP15 transcription factor from Trichoderma asperellum ACCC30536 and its function under pathogenic toxin stress

机译:Trichoderma Asperellum ACCC30536的突出蛋白15转录因子分析及其在致病性毒素应力下的作用

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The TabZIP15 gene encoding a 396 amino acid (aa) polypeptide in the fungus Trichoderma asperellum ACCC30536 was cloned and characterised. The protein includes a basic region motif (NR-x2-QR-x2-R) and has a pillar-like structure. The 25 basic region/leucine zipper transcription factors (TFs) identified in the T. asperellum genome were divided into YAP (14 TFs), ATF2 (5), GCN4 (2), Zip1 (2), BRLZ (1) and u1 (1) subfamilies based on conserved domains. T. asperellum was cultured in minimal media (MM) control, C-Hungry and N-Hungry medium (to simulate nutrient competition and interaction with pathogens, respectively), and differential expression analysis showed that 14 TabZIP genes (including TabZIP15) were significantly altered under both conditions; TabZIP23 responded strongly to N-Hungry media and TabZIP24 responded strongly to C-Hungry media. However, only YAP genes TabZIP15, TabZIP12 and TabZIP2 were significantly upregulated under both conditions, and expression levels of TabZIP15 were highest. T. asperellum was also cultured in the presence of five fungal pathogenic toxins, and RT-qPCR results showed that TabZIP15 was significantly upregulated in four of the five toxin stress conditions (MM?+?Rhizoctonia solani, MM?+?Fusarium oxysporum, MM?+?Alternaria alternata and MM?+?Cytospora chrysosperma).
机译:克隆并表征编码在真菌Trichoderma asperellum ACCC30536中的396个氨基酸(AA)多肽的突出突突15基因。蛋白质包括碱性区域基序(NR-X2-QR-X2-R)并具有柱状结构。将T. asperellum基因组中鉴定的25个基本区域/亮氨酸拉链转录因子(TFS)分为YAP(14 TFS),ATF2(5),GCN4(2),ZIP1(2),BRLZ(1)和U1( 1)基于保守结构域的亚属。 T. asperellum在最小培养基(mm)对照中培养,C饥饿和N饥饿的培养基(分别模拟营养竞争和与病原体的相互作用)和差异表达分析显示,14个突出基因(包括偶氮15)显着改变在两个条件下; Tabzip23强烈响应N-Hungry Media,Tabzip24强烈响应C饥饿的媒体。然而,在两个条件下,只有yap基因Tabzip15,Tabzip12和Tabzip2显着上调,Tabzip15的表达水平最高。在五种真菌病原毒素的存在下也培养了叶片,RT-QPCR结果表明,在五种毒素胁迫条件下的四种(mMγ+ + rhizoctonia solani,mm?o usarium oxysporum,mm ?+?alertaria alternata和mm?+?cytospora chrysosperma)。

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