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Comprehensive Assessment of Candidate Reference Genes for Gene Expression Studies Using RT-qPCR in Tamarixia radiata, a Predominant Parasitoid of Diaphorina citri.
Guo, Chang-Fei; Pan, Hui-Peng; Zhang, Li-He; Ou, Da; Lu, Zi-Tong; Khan, Muhammad Musa; Qiu, Bao-Li.
Afiliación
  • Guo CF; Key Laboratory of Bio-Pesticide Innovation and Application of Guangdong Province, South China Agricultural University, Guangzhou 510642, China.
  • Pan HP; Engineering Research Center of Biocontrol, Ministry of Education, Guangzhou 510642, China.
  • Zhang LH; Key Laboratory of Bio-Pesticide Innovation and Application of Guangdong Province, South China Agricultural University, Guangzhou 510642, China.
  • Ou D; Engineering Research Center of Biocontrol, Ministry of Education, Guangzhou 510642, China.
  • Lu ZT; Key Laboratory of Bio-Pesticide Innovation and Application of Guangdong Province, South China Agricultural University, Guangzhou 510642, China.
  • Khan MM; Engineering Research Center of Biocontrol, Ministry of Education, Guangzhou 510642, China.
  • Qiu BL; Key Laboratory of Bio-Pesticide Innovation and Application of Guangdong Province, South China Agricultural University, Guangzhou 510642, China.
Genes (Basel) ; 11(10)2020 10 10.
Article en En | MEDLINE | ID: mdl-33050374
Tamarixia radiata (Waterston) is a predominant parasitoid of the Asian citrus psyllid (ACP), a destructive citrus pest and vector of huanglongbing (HLB) disease in the fields of southern China. To explore the functioning of target genes in T. radiata, the screening of specific reference genes is critical for carrying out the reverse transcriptase-quantitative polymerase chain reaction (RT-qPCR) under different experimental conditions. However, no reference gene(s) for T. radiata has yet been reported. Here, we selected seven housekeeping genes of T. radiate and evaluated their stability under the six conditions (developmental stage, sex, tissue, population, temperature, diet) by using RefFinder software, which contains four different programs (geNorm, ΔCt, BestKeeper, and NormFinder). Pairwise variation was analyzed by geNorm software to determine the optimal number of reference genes during the RT-qPCR analysis. The results reveal better reference genes for differing research foci: 18S and EF1A for the developmental stage; PRS18 and EF1A for sex, PRS18 and RPL13 for different tissues (head, thorax, abdomen); EF1A and ArgK between two populations; ß-tubulin and EF1A for different temperatures (5, 15, 25, 35 °C); and ArgK and PRS18 for different feeding diets. Furthermore, when the two optimal and two most inappropriate reference genes were chosen in different temperatures and tissue treatments, respectively, the corresponding expression patterns of HSP70 (as the reporter gene) differed substantially. Our study provides, for the first time, a more comprehensive list of optimal reference genes from T. radiata for use in RT-qPCR analysis, which should prove beneficial for subsequent functional investigations of target gene(s) in this natural enemy of ACP.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Proteínas de Insectos / Perfilación de la Expresión Génica / Reacción en Cadena en Tiempo Real de la Polimerasa / Hemípteros Idioma: En Revista: Genes (Basel) Año: 2020 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Proteínas de Insectos / Perfilación de la Expresión Génica / Reacción en Cadena en Tiempo Real de la Polimerasa / Hemípteros Idioma: En Revista: Genes (Basel) Año: 2020 Tipo del documento: Article