Wang Heng, Tong Wei, Feng Li, Jiao Qian, Long Li, Fang Rongjun, Zhao Weiguo
Bioorg Khim. 2014 Jul-Aug;40(4):458-67.
A large-scale RNA sequencing (RNA-seq) of mulberry (Morus L.) was carried out between two samples in regular and drought stress condition. In this research, de novo assembly was performed, and totally 54736 contigs were obtained from the reads, including the scaffolded regions. 1051 genes were identified that were significantly differently expressed between the two samples. As determined by Gene Ontology (GO) annotation and the Kyoto Encyclopedia of Genes and Genomes pathway mapping, 10110 GO terms and 247 pathways were assigned and then analyzed. Thousands of SSR markers produced in this study will enable genetic linkage mapping construction and gene-based association studies. Seven unique genes showing different expression level in control and drought stress groups were subsequently analyzed and identified by real-time PCR. For lack of mulberry whole genome information, transcriptome and de novo analysis from the two samples will provide important and useful information for later research and help genetic breeding of mulberry.
在正常和干旱胁迫条件下,对两个桑(桑属)样本进行了大规模RNA测序(RNA-seq)。本研究进行了从头组装,从读取序列中总共获得了54736个重叠群,包括支架区域。鉴定出1051个基因在两个样本之间存在显著差异表达。通过基因本体论(GO)注释和京都基因与基因组百科全书通路映射确定,分配了10110个GO术语和247条通路并进行了分析。本研究产生的数千个SSR标记将有助于构建遗传连锁图谱和基于基因的关联研究。随后通过实时PCR分析并鉴定了七个在对照和干旱胁迫组中显示不同表达水平的独特基因。由于缺乏桑的全基因组信息,对这两个样本的转录组和从头分析将为后续研究提供重要且有用的信息,并有助于桑的遗传育种。