Identification and validation of reference genes for qRT-PCR analysis in mulberry (Morus alba L.)

被引:15
|
作者
Dai, Fanwei [1 ,2 ]
Zhao, Xiting [3 ]
Tang, Cuiming [1 ,2 ]
Wang, Zhenjiang [1 ,2 ]
Kuang, Zheshi [1 ,2 ]
Li, Zhiyi [1 ]
Huang, Jing [1 ]
Luo, Guoqing [1 ,2 ]
机构
[1] Guangdong Acad Agr Sci, Sericultural & Agri Food Res Inst, Guangzhou, Guangdong, Peoples R China
[2] Minist Agr, Key Lab Urban Agr South China, Guangzhou, Guangdong, Peoples R China
[3] Henan Normal Univ, Coll Life Sci, Xinxiang, Peoples R China
来源
PLOS ONE | 2018年 / 13卷 / 03期
关键词
GENOME-WIDE IDENTIFICATION; BIOSYNTHETIC GENES; EXPRESSION; NORMALIZATION; SELECTION; CLONING;
D O I
10.1371/journal.pone.0194129
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
Mulberry (Morus alba L.) is an important economic tree species in many countries. Quantitative real time PCR (qRT-PCR) has become a widely used method for gene expression studies in plants. A suitable reference gene is essential to ensure accurate and reliable results for qRT-PCR analyses. However, no reports describing the selection of reference genes have been published for mulberry. In this work, we evaluated the stability of twenty candidate reference genes in different plant tissues and under different stress conditions by qRTPCR in mulberry using algorithms in two programs geNorm and NormFinder. The results revealed that TUB2, UBI4, ACTIN3 and RPL4 were ranked as the most stable reference genes in the samples subsets, whereas EF1a4 and TUB3showed the least stability with both algorithms. To further validate the stability of the reference genes, the expression patterns of six genes of mulberry were analyzed by normalization with the selected reference genes. Our study will benefit future analyses of gene expression in mulberry.
引用
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页数:14
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