首页> 外文期刊>Journal of Insect Science >Identification and Evaluation of Suitable Reference Genes for Normalization of MicroRNA Expression in Helicoverpa armigera (Lepidoptera: Noctuidae) Using Quantitative Real-Time PCR
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Identification and Evaluation of Suitable Reference Genes for Normalization of MicroRNA Expression in Helicoverpa armigera (Lepidoptera: Noctuidae) Using Quantitative Real-Time PCR

机译:使用定量实时荧光定量PCR鉴定和评估棉铃虫中MicroRNA表达正常化的合适参考基因

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More and more studies have focused on microRNAs (miRNAs) expression in the pest Helicoverpa armigera (Lepidoptera: Noctuidae) recently. Quantitative real-time PCR (qRT-PCR) is being widely used in miRNA expression studies. Suitable reference genes are necessary for the correct analysis of results. In this study, 10 candidate genes of H. armigera were selected and analyzed for their expression stability under different biotic and abiotic conditions with 3 statistical methods, including geNorm, NormFinder, and Bestkeeper. Combination the best number of reference genes was calculated by geNorm. One target gene, let-7, was used to validate the selection of reference genes. The suitable candidate reference genes were shown as follows: miR-9 and U6 snRNA for developmental stages, miR-100 and U6 snRNA for larval tissues, miR-100 and miR-305 for adult tissues, miR-9 and miR-279 for parasitic treatment, miR-998 and U6 snRNA for nuclear polyhedrosis virus infection, miR-9 and U6 snRNA for insecticide treatment, miR-92a, miR-100, and miR-279 for temperature treatment, miR-92a, miR-305, and miR-998 for starvation treatment, miR-9 and miR-279 for light treatment, miR-305 and miR-998 for hormone treatment, and there was not one reference gene suitable for all samples. This study could promote future research on miRNAs expression in H. armigera with optimal reference genes under different experimental conditions.
机译:最近,越来越多的研究集中在棉铃虫(Helicoverpa armigera)(鳞翅目:夜蛾科)中的microRNA(miRNA)表达上。实时定量PCR(qRT-PCR)被广泛用于miRNA表达研究。正确的结果分析需要合适的参考基因。在这项研究中,选择了棉铃虫的10个候选基因,并使用geNorm,NormFinder和Bestkeeper等3种统计方法分析了它们在不同生物和非生物条件下的表达稳定性。 geNorm计算出最佳的参考基因数量。一种靶基因let-7被用于验证参考基因的选择。合适的候选参考基因如下:发育阶段的miR-9和U6 snRNA,幼虫组织的miR-100和U6 snRNA,成人组织的miR-100和miR-305,寄生虫的miR-9和miR-279处理,用于核多角体病毒感染的miR-998和U6 snRNA,用于杀虫剂处理的miR-9和U6 snRNA,用于温度处理的miR-92a,miR-100和miR-279,miR-92a,miR-305和miR -998用于饥饿处理,miR-9和miR-279用于光处理,miR-305和miR-998用于激素处理,并且没有一个适用于所有样品的参考基因。这项研究可以促进今后在不同实验条件下使用最佳参考基因在棉铃虫中表达miRNA的研究。

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