Jia Tianqi, Wei Danfeng, Meng Shan, Allan Andrew C, Zeng Lihui
College of Horticulture, Fujian Agriculture and Forestry University, Fuzhou, Fujian, P. R. China.
The New Zealand Institute for Plant & Food Research Limited (Plant & Food Research), Mt Albert, Auckland, New Zealand.
PLoS One. 2014 Dec 5;9(12):e114568. doi: 10.1371/journal.pone.0114568. eCollection 2014.
Longan (Dimocarpus longan L.) is a tropical/subtropical fruit tree of significant economic importance in Southeast Asia. However, a lack of transcriptomic and genomic information hinders research on longan traits, such as the control of flowering. In this study, high-throughput RNA sequencing (RNA-Seq) was used to investigate differentially expressed genes between a unique longan cultivar 'Sijimi'(S) which flowers throughout the year and a more typical cultivar 'Lidongben'(L) which flowers only once in the season, with the aim of identifying candidate genes associated with continuous flowering. 36,527 and 40,982 unigenes were obtained by de novo assembly of the clean reads from cDNA libraries of L and S cultivars. Additionally 40,513 unigenes were assembled from combined reads of these libraries. A total of 32,475 unigenes were annotated by BLAST search to NCBI non-redundant protein (NR), Swiss-Prot, Clusters of Orthologous Groups (COGs) and Kyoto Encyclopedia of Genes and Genomes (KEGG) databases. Of these, almost fifteen thousand unigenes were identified as significantly differentially expressed genes (DEGs) by using Reads Per kb per Million reads (RPKM) method. A total of 6,415 DEGs were mapped to 128 KEGG pathways, and 8,743 DEGs were assigned to 54 Gene Ontology categories. After blasting the DEGs to public sequence databases, 539 potential flowering-related DEGs were identified. In addition, 107 flowering-time genes were identified in longan, their expression levels between two longan samples were compared by RPKM method, of which the expression levels of 15 were confirmed by real-time quantitative PCR. Our results suggest longan homologues of SHORT VEGETATIVE PHASE (SVP), GIGANTEA (GI), F-BOX 1 (FKF1) and EARLY FLOWERING 4 (ELF4) may be involved this flowering trait and ELF4 may be a key gene. The identification of candidate genes related to continuous flowering will provide new insight into the molecular process of regulating flowering time in woody plants.
龙眼(Dimocarpus longan L.)是一种在东南亚具有重要经济价值的热带/亚热带果树。然而,转录组和基因组信息的缺乏阻碍了对龙眼性状(如开花调控)的研究。在本研究中,采用高通量RNA测序(RNA-Seq)技术,对一种全年开花的独特龙眼品种‘四季蜜’(S)和一个更典型的季节性单花品种‘立冬本’(L)之间的差异表达基因进行了研究,旨在鉴定与连续开花相关的候选基因。通过对L和S品种cDNA文库的clean reads进行从头组装,分别获得了36,527和40,982个单基因。此外,从这些文库的混合reads中组装出40,513个单基因。通过BLAST搜索NCBI非冗余蛋白质(NR)、Swiss-Prot、直系同源簇(COGs)和京都基因与基因组百科全书(KEGG)数据库,对总共32,475个单基因进行了注释。其中,通过每百万reads中每kb的reads数(RPKM)方法,鉴定出近一万五千个单基因为显著差异表达基因(DEGs)。共有6,415个DEGs被映射到128条KEGG通路,8,743个DEGs被分配到54个基因本体类别。将DEGs与公共序列数据库进行比对后,鉴定出539个潜在的与开花相关的DEGs。此外,在龙眼中鉴定出107个开花时间基因,通过RPKM方法比较了两个龙眼样本之间它们的表达水平,其中15个的表达水平通过实时定量PCR得到了证实。我们的结果表明,SHORT VEGETATIVE PHASE(SVP)、GIGANTEA(GI)、F-BOX 1(FKF1)和EARLY FLOWERING 4(ELF4)的龙眼同源物可能参与了这种开花性状,并且ELF4可能是关键基因。与连续开花相关的候选基因的鉴定将为木本植物开花时间调控的分子过程提供新的见解。