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Comprehensive Evaluation of Candidate Reference Genes for QRT-PCR Studies of Gene Expression in Mustard Aphid, Lipaphis Erysimi (Kalt)

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Journal Sci Rep
Specialty Science
Date 2016 May 12
PMID 27165720
Citations 47
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Abstract

Mustard aphid, also known as turnip aphid (Lipaphis erysimi) is a major insect pest of rapeseed-mustard group of crops. Tremendous economic significance has led to substantial basic research involving gene-expression studies in this insect species. In qRT-PCR analysis of gene-expression, normalization of data against RNA variation by using appropriate reference gene is fundamental. However, appropriate reference genes are not known in case of L. erysimi. We evaluated 11 candidate reference genes for their expression stability in 21 samples of L. erysimi subjected to various regimes of experimental treatments. Unlike other studies, we validated true effects of the treatments on the samples either by gene-expression study of an associated marker gene or by biochemical tests. In the validated samples, expression stability of the reference genes was analysed by employing four different statistical softwares geNorm, NormFinder, BestKeeper and deltaCt. Drawing consensus on the results from different softwares, we recommend three best reference genes 16S, RPS18 and RPL13 for normalization of qRT-PCR data in L. erysimi. This study provides for the first time a comprehensive list of suitable reference genes for mustard aphid and demonstrates the advantage of using more than one reference gene in combination for certain experimental conditions.

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References
1.
Xiao X, Ma J, Wang J, Wu X, Li P, Yao Y . Validation of suitable reference genes for gene expression analysis in the halophyte Salicornia europaea by real-time quantitative PCR. Front Plant Sci. 2015; 5:788. PMC: 4300904. DOI: 10.3389/fpls.2014.00788. View

2.
Mao J, Zeng F . Plant-mediated RNAi of a gap gene-enhanced tobacco tolerance against the Myzus persicae. Transgenic Res. 2013; 23(1):145-52. DOI: 10.1007/s11248-013-9739-y. View

3.
Vandesompele J, De Preter K, Pattyn F, Poppe B, Van Roy N, De Paepe A . Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome Biol. 2002; 3(7):RESEARCH0034. PMC: 126239. DOI: 10.1186/gb-2002-3-7-research0034. View

4.
Yuan M, Lu Y, Zhu X, Wan H, Shakeel M, Zhan S . Selection and evaluation of potential reference genes for gene expression analysis in the brown planthopper, Nilaparvata lugens (Hemiptera: Delphacidae) using reverse-transcription quantitative PCR. PLoS One. 2014; 9(1):e86503. PMC: 3900570. DOI: 10.1371/journal.pone.0086503. View

5.
Furch A, van Bel A, Will T . Aphid salivary proteases are capable of degrading sieve-tube proteins. J Exp Bot. 2014; 66(2):533-9. DOI: 10.1093/jxb/eru487. View