College of Forestry, Shandong Agricultural University, Tai'an, Shandong Province, China.
State Forestry and Grassland Administr, ation Key Laboratory of Silviculture inthe Downstream Areas of the Yellow River, Shandong Agricultural University, Tai'an, Shandong Province, China.
BMC Plant Biol. 2021 May 31;21(1):249. doi: 10.1186/s12870-021-03042-1.
Walnut anthracnose induced by Colletotrichum gloeosporioides is a disastrous disease affecting walnut production. The resistance of walnut fruit to C. gloeosporioides is a highly complicated and genetically programmed process. However, the underlying mechanisms have not yet been elucidated.
To understand the molecular mechanism underlying the defense of walnut to C. gloeosporioides, we used RNA sequencing and label-free quantitation technologies to generate transcriptomic and proteomic profiles of tissues at various lifestyle transitions of C. gloeosporioides, including 0 hpi, pathological tissues at 24 hpi, 48 hpi, and 72 hpi, and distal uninoculated tissues at 120 hpi, in anthracnose-resistant F26 fruit bracts and anthracnose-susceptible F423 fruit bracts, which were defined through scanning electron microscopy. A total of 21,798 differentially expressed genes (DEGs) and 1929 differentially expressed proteins (DEPs) were identified in F26 vs. F423 at five time points, and the numbers of DEGs and DEPs were significantly higher in the early infection stage. Using pairwise comparisons and weighted gene co-expression network analysis of the transcriptome, we identified two modules significantly related to disease resistance and nine hub genes in the transcription expression gene networks. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analysis of the DEGs and DEPs revealed that many genes were mainly related to immune response, plant hormone signal transduction, and secondary metabolites, and many DEPs were involved in carbon metabolism and photosynthesis. Correlation analysis between the transcriptome data and proteome data also showed that the consistency of the differential expression of the mRNA and corresponding proteins was relatively higher in the early stage of infection.
Collectively, these results help elucidate the molecular response of walnut fruit to C. gloeosporioides and provide a basis for the genetic improvement of walnut disease resistance.
由胶孢炭疽菌引起的核桃炭疽病是一种严重影响核桃生产的灾难性疾病。核桃果实对 C. gloeosporioides 的抗性是一个高度复杂和遗传编程的过程。然而,其潜在机制尚未阐明。
为了了解核桃对 C. gloeosporioides 防御的分子机制,我们使用 RNA 测序和无标记定量技术生成了组织的转录组和蛋白质组图谱,这些组织处于 C. gloeosporioides 的各种生活方式转变中,包括 0 hpi、24 hpi、48 hpi 和 72 hpi 的病理组织,以及 120 hpi 时未接种的远组织,在抗炭疽病的 F26 果苞和易感炭疽病的 F423 果苞中,这些组织是通过扫描电子显微镜定义的。在五个时间点,F26 与 F423 相比,共鉴定出 21798 个差异表达基因(DEGs)和 1929 个差异表达蛋白(DEPs),在早期感染阶段,DEGs 和 DEPs 的数量明显更高。通过转录组的成对比较和加权基因共表达网络分析,我们在转录表达基因网络中鉴定出两个与抗病性显著相关的模块和 9 个枢纽基因。DEGs 和 DEPs 的基因本体论和京都基因与基因组百科全书分析表明,许多基因主要与免疫反应、植物激素信号转导和次生代谢物有关,许多 DEPs 参与碳代谢和光合作用。转录组数据和蛋白质组数据的相关性分析也表明,在感染早期,mRNA 和相应蛋白的差异表达一致性相对较高。
综上所述,这些结果有助于阐明核桃果实对 C. gloeosporioides 的分子反应,为核桃抗病性的遗传改良提供了基础。