identification of differentially-expressed genes associated with pistil abortion in japanese apricot by genome-wide transcriptional analysis识别差异表达基因与雌蕊有关堕胎的梅花全基因组转录分析.pdfVIP
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identification of differentially-expressed genes associated with pistil abortion in japanese apricot by genome-wide transcriptional analysis识别差异表达基因与雌蕊有关堕胎的梅花全基因组转录分析
Identification of Differentially-Expressed Genes Associated with Pistil Abortion in Japanese Apricot by Genome-Wide Transcriptional Analysis Ting Shi., Zhihong Gao*., Liangju Wang, Zhen Zhang, Weibing Zhuang, Hailong Sun, Wenjun Zhong College of Horticulture, Nanjing Agricultural University, Nanjing, People’s Republic China Abstract The phenomenon of pistil abortion widely occurs in Japanese apricot, and imperfect flowers with pistil abortion seriously decrease the yield in production. Although transcriptome analyses have been extensively studied in the past, a systematic study of differential gene expression has not been performed in Japanese apricot. To investigate genes related to the pistil development of Japanese apricot, high-throughput sequencing technology (Illumina) was employed to survey gene expression profiles from perfect and imperfect Japanese apricot flower buds. 3,476,249 and 3,580,677 tags were sequenced from two libraries constructed from perfect and imperfect flower buds of Japanese apricot, respectively. There were 689 significant differentially-expressed genes between the two libraries. GO annotation revealed that highly ranked genes were those implicated in small molecule metabolism, cellular component organisation or biogenesis at the cellular level and fatty acid metabolism. According to the results, we assumed that late embryogenesis abundant protein (LEA), Dicer-like 3 (DCL3) Xyloglucan endotransglucosylase/hydrolase 2 (XTH2), Pectin lyase-like superfamily protein (PPME1), Lipid transfer protein 3 (LTP3), Fatty acid biosynthesis 1 (FAB1) and Fatty acid desaturase 5 (FAD5) might have relationships with the pistil abortion in Japanese apricot. The expression patterns of 36 differentially expressed genes were confirmed by real-time (RT)-PCR. This is the first report of the Illumina RNA-seq technique being used for
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