Transcriptomic analysis of 'Suli' pear (Pyrus pyrifolia white pear group) buds during the dormancy by RNA-Seq

被引:149
作者
Liu, Guoqin [1 ,2 ]
Li, Wanshun [3 ]
Zheng, Penghua [1 ]
Xu, Tong [3 ]
Chen, Lijuan [3 ]
Liu, Dongfeng [1 ]
Hussain, Sayed [1 ]
Teng, Yuanwen [1 ]
机构
[1] Zhejiang Univ, Dept Hort, State Agr Minist, Key Lab Hort Plant Growth Dev & Qual Improvement, Hangzhou 310058, Zhejiang Provin, Peoples R China
[2] Guizhou Univ, Coll Agr, Guiyang 550025, Guizhou Provinc, Peoples R China
[3] BGI Tech, Shenzhen 518083, Guangdong Provi, Peoples R China
关键词
'Suli' pear (Pyrus pyrifolia white pear group); Transcriptome; Bud dormancy; RNA-Seq; UNDERGROUND ADVENTITIOUS BUDS; MADS-BOX GENES; PRUNUS-PERSICA; DIFFERENTIAL EXPRESSION; FRUIT-DEVELOPMENT; GROWTH CESSATION; CIRCADIAN CLOCK; CANDIDATE GENES; LOW-TEMPERATURE; JAPANESE PEAR;
D O I
10.1186/1471-2164-13-700
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Bud dormancy is a critical developmental process that allows perennial plants to survive unfavorable environmental conditions. Pear is one of the most important deciduous fruit trees in the world, but the mechanisms regulating bud dormancy in this species are unknown. Because genomic information for pear is currently unavailable, transcriptome and digital gene expression data for this species would be valuable resources to better understand the molecular and biological mechanisms regulating its bud dormancy. Results: We performed de novo transcriptome assembly and digital gene expression (DGE) profiling analyses of 'Suli' pear (Pyrus pyrifolia white pear group) using the Illumina RNA-seq system. RNA-Seq generated approximately 100 M high-quality reads that were assembled into 69,393 unigenes (mean length = 853 bp), including 14,531 clusters and 34,194 singletons. A total of 51,448 (74.1%) unigenes were annotated using public protein databases with a cut-off E-value above 10(-5). We mainly compared gene expression levels at four time-points during bud dormancy. Between Nov. 15 and Dec. 15, Dec. 15 and Jan. 15, and Jan. 15 and Feb. 15, 1,978, 1,024, and 3,468 genes were differentially expressed, respectively. Hierarchical clustering analysis arranged 190 significantly differentially-expressed genes into seven groups. Seven genes were randomly selected to confirm their expression levels using quantitative real-time PCR. Conclusions: The new transcriptomes offer comprehensive sequence and DGE profiling data for a dynamic view of transcriptomic variation during bud dormancy in pear. These data provided a basis for future studies of metabolism during bud dormancy in non-model but economically-important perennial species.
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页数:18
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