Chen Xuejing, Hao Xiaoran, Akhberdi Oren, Zhu Xudong
College of Biological and Geography Sciences, Yili Normal University, Yining 835000, China.
National Experimental Teaching Demonstrating Center, College of Life Sciences, Beijing Normal University, Beijing 100875, China.
J Fungi (Basel). 2023 Apr 27;9(5):520. doi: 10.3390/jof9050520.
(teleomorph ) is the causal agent of sunflower ( L.) black stem. In order to investigate the molecular basis for the pathogenicity of , genomic and transcriptomic analyses were performed. The genome size was 38.24 Mb and assembled into 27 contigs with 11,094 putative predicted genes. These include 1133 genes for CAZymes specific for plant polysaccharide degradation, 2356 for the interaction between the pathogen and host, 2167 for virulence factors, and 37 secondary metabolites gene clusters. RNA-seq analysis was conducted at the early and late stages of the fungal spot formation in infected sunflower tissues. A total of 2506, 3035, and 2660 differentially expressed genes (DEGs) between CT and each treatment group (LEAF-2d, LEAF-6d, and STEM) were retrieved, respectively. The most significant pathways of DEGs from these diseased sunflower tissues were the metabolic pathways and biosynthesis of secondary metabolites. Overall, 371 up-regulated DEGs were shared among LEAF-2d, LEAF-6d, and STEM, including 82 mapped to DFVF, 63 mapped to PHI-base, 69 annotated as CAZymes, 33 annotated as transporters, 91 annotated as secretory proteins, and a carbon skeleton biosynthetic gene. The most important DEGs were further confirmed by RT-qPCR. This is the first report on the genome-scale assembly and annotation for . Our data provide a framework for further revealing the underlying mechanism of the pathogenesis of , and also suggest the potential targets for the diseases caused by this fungal pathogen.
(有性型)是向日葵(L.)黑茎病的病原菌。为了研究其致病的分子基础,进行了基因组和转录组分析。基因组大小为38.24 Mb,组装成27个重叠群,有11094个推定预测基因。其中包括1133个参与植物多糖降解的碳水化合物活性酶基因、2356个参与病原菌与寄主相互作用的基因、2167个毒力因子基因以及37个次生代谢物基因簇。在感染向日葵组织中真菌斑点形成的早期和晚期进行了RNA测序分析。分别在CT与每个处理组(LEAF - 2d、LEAF - 6d和STEM)之间检索到2506、3035和2660个差异表达基因(DEG)。这些患病向日葵组织中差异表达基因最显著的途径是代谢途径和次生代谢物的生物合成。总体而言,LEAF - 2d、LEAF - 6d和STEM之间共有371个上调的差异表达基因,其中82个映射到DFVF,63个映射到PHI - base,69个注释为碳水化合物活性酶,33个注释为转运蛋白,91个注释为分泌蛋白,还有一个碳骨架生物合成基因。通过RT - qPCR进一步证实了最重要的差异表达基因。这是关于该病原菌基因组规模组装和注释的首次报道。我们的数据为进一步揭示其致病的潜在机制提供了框架,也为这种真菌病原菌引起的疾病提供了潜在靶点。