Assessment of reference gene stability in Rice stripe virus and Rice black streaked dwarf virus infection rice by quantitative Real-time PCR

被引:27
作者
Fang, Peng [1 ,2 ,3 ]
Lu, Rongfei [3 ]
Sun, Feng [1 ,2 ]
Lan, Ying [1 ,2 ]
Shen, Wenbiao [3 ]
Du, Linlin [1 ,2 ]
Zhou, Yijun [1 ,2 ]
Zhou, Tong [1 ,2 ]
机构
[1] Jiangsu Acad Agr Sci, Inst Plant Protect, Nanjing 210014, Jiangsu, Peoples R China
[2] Minist Agr, Sci Observing & Expt Stn Crop Pests Nanjing, Nanjing 210014, Peoples R China
[3] Nanjing Agr Univ, Coll Life Sci, Nanjing 210095, Jiangsu, Peoples R China
关键词
Gene expression; RT-qPCR; Reference genes; RSV- and RBSDV-infected rice; POLYMERASE-CHAIN-REACTION; RT-PCR; SYSTEMATIC VALIDATION; HOUSEKEEPING GENES; EXPRESSION; DISEASE; NORMALIZATION; QUANTIFICATION; IDENTIFICATION; RESISTANCE;
D O I
10.1186/s12985-015-0405-2
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Stably expressed reference gene(s) normalization is important for the understanding of gene expression patterns by quantitative Real-time PCR (RT-qPCR), particularly for Rice stripe virus (RSV) and Rice black streaked dwarf virus (RBSDV) that caused seriously damage on rice plants in China and Southeast Asia. Methods: The expression of fourteen common used reference genes of Oryza sativa L. were evaluated by RT-qPCR in RSV and RBSDV infected rice plants. Suitable normalization reference gene(s) were identified by geNorm and NormFinder algorithms. Results: UBQ 10 + GAPDH and UBC + Actin1 were identified as suitable reference genes for RT-qPCR normalization under RSV and RBSDV infection, respectively. When using multiple reference genes, the expression patterns of OsPRIb and OsWRKY, two virus resistance genes, were approximately similar with that reported previously. Comparatively, by using single reference gene (TIP41-Like), a weaker inducible response was observed. Conclusions: We proposed that the combination of two reference genes could obtain more accurate and reliable normalization of RT-qPCR results in RSV- and RBSDV-infected plants. This work therefore sheds light on establishing a standardized RT-qPCR procedure in RSV-and RBSDV-infected rice plants, and might serve as an important point for discovering complex regulatory networks and identifying genes relevant to biological processes or implicated in virus.
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页数:11
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