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Identification and Validation of Reference Genes for QRT-PCR Studies of the Obligate Aphid Pathogenic Fungus Pandora Neoaphidis During Different Developmental Stages

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Journal PLoS One
Date 2017 Jul 4
PMID 28672012
Citations 3
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Abstract

The selection of stable reference genes is a critical step for the accurate quantification of gene expression. To identify and validate the reference genes in Pandora neoaphidis-an obligate aphid pathogenic fungus-the expression of 13classical candidate reference genes were evaluated by quantitative real-time reverse transcriptase polymerase chain reaction(qPCR) at four developmental stages (conidia, conidia with germ tubes, short hyphae and elongated hyphae). Four statistical algorithms, including geNorm, NormFinder, BestKeeper and Delta Ct method were used to rank putative reference genes according to their expression stability and indicate the best reference gene or combination of reference genes for accurate normalization. The analysis of comprehensive ranking revealed that ACT1and 18Swas the most stably expressed genes throughout the developmental stages. To further validate the suitability of the reference genes identified in this study, the expression of cell division control protein 25 (CDC25) and Chitinase 1(CHI1) genes were used to further confirm the validated candidate reference genes. Our study presented the first systematic study of reference gene(s) selection for P. neoaphidis study and provided guidelines to obtain more accurate qPCR results for future developmental efforts.

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References
1.
Fang W, Bidochka M . Expression of genes involved in germination, conidiogenesis and pathogenesis in Metarhizium anisopliae using quantitative real-time RT-PCR. Mycol Res. 2006; 110(Pt 10):1165-71. DOI: 10.1016/j.mycres.2006.04.014. View

2.
Kianianmomeni A, Hallmann A . Validation of reference genes for quantitative gene expression studies in Volvox carteri using real-time RT-PCR. Mol Biol Rep. 2013; 40(12):6691-9. DOI: 10.1007/s11033-013-2784-z. View

3.
De Fine Licht H, Hajek A, Eilenberg J, Jensen A . Utilizing Genomics to Study Entomopathogenicity in the Fungal Phylum Entomophthoromycota: A Review of Current Genetic Resources. Adv Genet. 2016; 94:41-65. DOI: 10.1016/bs.adgen.2016.01.003. View

4.
Teste M, Duquenne M, Francois J, Parrou J . Validation of reference genes for quantitative expression analysis by real-time RT-PCR in Saccharomyces cerevisiae. BMC Mol Biol. 2009; 10:99. PMC: 2776018. DOI: 10.1186/1471-2199-10-99. View

5.
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