Selection of reference genes for miRNA qRT-PCR under abiotic stress in grapevine

被引:70
|
作者
Luo, Meng [1 ,2 ]
Gao, Zhen [1 ,2 ]
Li, Hui [1 ,2 ]
Li, Qin [1 ,2 ]
Zhang, Caixi [1 ,2 ]
Xu, Wenping [1 ,2 ]
Song, Shiren [1 ,2 ]
Ma, Chao [1 ,2 ]
Wang, Shiping [1 ,2 ,3 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Agr & Biol, Dept Plant Sci, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Agr & Biol, Ctr Viticulture & Enol, Shanghai 200240, Peoples R China
[3] Shandong Acad Agr Sci, Key Lab Agroprod Proc Technol Shandong, Inst Agrofood Sci & Technol, Jinan 250100, Shandong, Peoples R China
来源
SCIENTIFIC REPORTS | 2018年 / 8卷
关键词
INNER REFERENCE GENES; REAL-TIME PCR; MICRORNA EXPRESSION; CLIMATE-CHANGE; SMALL RNAS; RT-PCR; DROUGHT; NORMALIZATION; RESPONSES; TRANSCRIPTOME;
D O I
10.1038/s41598-018-22743-6
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Grapevine is among the fruit crops with high economic value, and because of the economic losses caused by abiotic stresses, the stress resistance of Vitis vinifera has become an increasingly important research area. Among the mechanisms responding to environmental stresses, the role of miRNA has received much attention recently. qRT-PCR is a powerful method for miRNA quantitation, but the accuracy of the method strongly depends on the appropriate reference genes. To determine the most suitable reference genes for grapevine miRNA qRT-PCR, 15 genes were chosen as candidate reference genes. After eliminating 6 candidate reference genes with unsatisfactory amplification efficiency, the expression stability of the remaining candidate reference genes under salinity, cold and drought was analysed using four algorithms, geNorm, NormFinder, deltaCt and Bestkeeper. The results indicated that U6 snRNA was the most suitable reference gene under salinity and cold stresses; whereas miR168 was the best for drought stress. The best reference gene sets for salinity, cold and drought stresses were miR160e + miR164a, miR160e + miR168 and ACT + UBQ + GAPDH, respectively. The selected reference genes or gene sets were verified using miR319 or miR408 as the target gene.
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页数:11
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