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Reference genes selection for quantitative gene expression studies in tea green leafhoppers, Empoasca onukii Matsuda

机译:茶绿叶蝉(Empoasca onukii Matsuda)中定量基因表达研究的参考基因选择

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摘要

Empoasca onukii Matsuda is one of the most devastating pests of the tea plant (Camellia sinensis). Still, the presumed expression stability of its reference genes (RGs) has not been analyzed. RGs are essential for accurate and reliable gene expression analysis, so this absence has hampered the study of the insect’s molecular biology. To find candidate RGs for normalizing gene expression data, we cloned ten common housekeeping genes from E. onukii. Using the ΔCt method, geNorm, NormFinder and BestKeeper, we screened the RGs that were appropriate for quantifying the mRNA transcription of cellular responses under five experimental conditions. We identified the combinations of α-TUB and G6PDH, α-TUB and UBC, two RGs (α-TUB and β-TUB1) or three RGs (α-TUB, RPL13 and GAPDH), AK and UBC, or RPL13 and α-TUB as the best for analyzing gene expression in E. onukii adults of both sexes in different tissues, nymphs at different developmental stages, nymphs exposed to different temperatures or nymphs exposed to photoperiod stress. Finally, the E. onukii cysteine proteinase (Eocyp) was chosen as the target gene to validate the rationality of the proposed RGs. In conclusion, our study suggests a series of RGs with which to study the gene expression profiles of E. onukii that have been manipulated (biotically or abiotically) using reverse transcription quantitative polymerase chain reaction. The results offer a solid foundation for further studies of the molecular biology of E. onukii.
机译:Empoasca onukii Matsuda是茶树(山茶)中最具破坏力的害虫之一。仍然,尚未分析其参考基因(RGs)的假定表达稳定性。 RG对于准确和可靠的基因表达分析至关重要,因此,这种缺失阻碍了对昆虫分子生物学的研究。为了找到用于标准化基因表达数据的候选RG,我们从onukii克隆了10个常见的管家基因。使用ΔCt方法,geNorm,NormFinder和BestKeeper,我们筛选了适合定量在五个实验条件下细胞反应的mRNA转录的RG。我们确定了α-TUB和G6PDH,α-TUB和UBC,两个RG(α-TUB和β-TUB1)或三个RG(α-TUB,RPL13和GAPDH),AK和UBC或RPL13和α- TUB 是分析 E 中基因表达的最佳方法。雌雄各异,在不同的组织,若虫处于不同的发育阶段,若虫处于不同温度下或若虫处于光周期压力下。最后是 E 。以 onukii 半胱氨酸蛋白酶( Eocyp )为靶基因,验证了提出的RG的合理性。总之,我们的研究提出了一系列RG,用于研究 E 的基因表达谱。使用反转录定量聚合酶链反应(生物或非生物)进行操作的 onukii 。研究结果为 E 的分子生物学研究提供了坚实的基础。 onukii

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