Key Lab of Sugarcane Biology and Genetic Breeding, Ministry of Agriculture, Fujian Agriculture and Forestry University, Fuzhou, Fujian 350002, China.
Biomed Res Int. 2013;2013:298920. doi: 10.1155/2013/298920. Epub 2013 Oct 23.
To understand the molecular basis of sugarcane-smut interaction, it is important to identify sugarcane genes that respond to the pathogen attack. High-throughput tag-sequencing (tag-seq) analysis by Solexa technology was performed on sugarcane infected with Sporisorium scitaminea, which should have massively increased the amount of data available for transcriptome profile analysis. After mapping to sugarcane EST databases in NCBI, we obtained 2015 differentially expressed genes, of which 1125 were upregulated and 890 downregulated by infection. Gene ontology (GO) analysis revealed that the differentially expressed genes involve in many cellular processes. Pathway analysis revealed that metabolic pathways and ribosome function are significantly affected, where upregulation of expression dominates over downregulation. Differential expression of three candidate genes involved in MAP kinase signaling pathway, ScBAK1 (GenBank Accession number: KC857629), ScMapkk (GenBank Accession number: KC857627), and ScGloI (GenBank Accession number: KC857628), was confirmed by reverse transcription polymerase chain reaction (RT-PCR). Real-time quantitative PCR (qRT-PCR) analysis concluded that the expression of these genes were all up-regulated after the infection of S. scitaminea and may play a role in pathogen response in sugarcane. The present study provides insights into the molecular mechanism of sugarcane defense to S. scitaminea infection, leading to a more comprehensive understanding of sugarcane-smut interaction.
为了理解甘蔗与黑粉菌互作的分子基础,鉴定对病原菌攻击产生响应的甘蔗基因非常重要。利用 Solexa 技术进行了高通量标签测序(tag-seq)分析,对感染盾孢霉的甘蔗进行了分析,这应该大大增加了转录组谱分析可用的数据量。在将数据映射到 NCBI 中的甘蔗 EST 数据库后,我们获得了 2015 个差异表达基因,其中 1125 个基因在感染后上调,890 个基因下调。基因本体(GO)分析表明,差异表达基因涉及许多细胞过程。途径分析表明,代谢途径和核糖体功能受到显著影响,其中表达上调占主导地位。参与 MAP 激酶信号通路的三个候选基因 ScBAK1(GenBank 登录号:KC857629)、ScMapkk(GenBank 登录号:KC857627)和 ScGloI(GenBank 登录号:KC857628)的差异表达通过反转录聚合酶链反应(RT-PCR)得到了证实。实时定量 PCR(qRT-PCR)分析得出结论,这些基因在感染盾孢霉后均上调表达,可能在甘蔗对病原菌的响应中发挥作用。本研究为甘蔗对盾孢霉感染的防御分子机制提供了深入了解,从而更全面地理解甘蔗黑粉病互作。