Chen Yuning, Ren Xiaoping, Zhou Xiaojing, Huang Li, Yan Liying, Lei Yong, Liao Boshou, Huang Jinyong, Huang Shunmou, Wei Wenhui, Jiang Huifang
Oil Crop Research Institute, Chinese Academy of Agricultural Sciences/Key Laboratory of Biology and Genetic Improvement of Oil Crops, Ministry of Agriculture, No 2 Xudong Second Road, Wuhan 430062, P,R, China.
BMC Genomics. 2014 Dec 7;15(1):1078. doi: 10.1186/1471-2164-15-1078.
Bacterial wilt caused by Ralstonia solanacearum is a serious soil-borne disease of peanut (Arachis hypogaea L). The molecular basis of peanut response to R. solanacearum remains unknown. To understand the resistance mechanism behind peanut resistance to R. solanacearum, we used RNA-Seq to perform global transcriptome profiling on the roots of peanut resistant (R) and susceptible (S) genotypes under R. solanacearum infection.
A total of 4.95 x 108 raw sequence reads were generated and subsequently assembled into 271, 790 unigenes with an average length of 890 bp and a N50 of 1, 665 bp. 179, 641 unigenes could be annotated by public protein databases. The pairwise transcriptome comparsions of time course (6, 12, 24, 48 and 72 h post inoculation) were conducted 1) between inoculated and control samples of each genotype, 2) between inoculated samples of R and S genotypes. The linear dynamics of transcriptome profile was observed between adjacent samples for each genotype, two genotypes shared similar transcriptome pattern at early time points with most significant up regulation at 12 hour, and samples from R genotype at 24 h and S genotype at 48 h showed similar transcriptome pattern, significant differences of transcriptional profile were observed in pairwise comparisons between R and S genotypes. KEGG analysis showed that the primary metabolisms were inhibited in both genotypes and stronger inhibition in R genotype post inoculation. The defense related genes (R gene, LRR-RLK, cell wall genes, etc.) generally showed a genotype-specific down regulation and different expression between both genotypes.
This transcriptome profiling provided the largest data set that explores the dynamic in crosstalk between peanut and R. solanacearum. The results suggested that the down-regulation of primary metabolism is contributed to the resistance difference between R and S genotypes. The genotype-specific expression pattern of defense related DEGs also contributed to the resistance difference between R and S genotype. This study will strongly contribute to better understand the molecular interaction between plant and R. solanacearum.
由青枯雷尔氏菌引起的青枯病是花生(Arachis hypogaea L)一种严重的土传病害。花生对青枯雷尔氏菌响应的分子基础尚不清楚。为了解花生对青枯雷尔氏菌抗性背后的抗性机制,我们利用RNA测序对青枯雷尔氏菌感染下花生抗性(R)和感病(S)基因型的根部进行了全转录组分析。
共产生了4.95×108条原始序列读数,随后组装成271790个单基因,平均长度为890 bp,N50为1665 bp。179641个单基因可通过公共蛋白质数据库进行注释。进行了时间进程(接种后6、12、24、48和72小时)的成对转录组比较:1) 每种基因型接种样本与对照样本之间;2) R和S基因型接种样本之间。观察到每种基因型相邻样本之间转录组图谱的线性动态变化,两种基因型在早期时间点具有相似的转录组模式,在12小时时上调最为显著,R基因型24小时和S基因型48小时的样本显示出相似的转录组模式,R和S基因型之间的成对比较中观察到转录图谱的显著差异。KEGG分析表明,两种基因型的初级代谢均受到抑制,接种后R基因型的抑制作用更强。防御相关基因(R基因、LRR-RLK、细胞壁基因等)通常表现出基因型特异性下调,且两种基因型之间表达不同。
该转录组分析提供了探索花生与青枯雷尔氏菌相互作用动态的最大数据集。结果表明,初级代谢的下调导致了R和S基因型之间的抗性差异。防御相关差异表达基因的基因型特异性表达模式也导致了R和S基因型之间的抗性差异。本研究将极大地有助于更好地理解植物与青枯雷尔氏菌之间的分子相互作用。