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用于韭菜迟眼蕈蚊(双翅目:眼蕈蚊科)定量实时PCR分析的管家基因评估

Evaluation of Housekeeping Genes for Quantitative Real-Time PCR Analysis of Bradysia odoriphaga (Diptera: Sciaridae).

作者信息

Shi Caihua, Yang Fengshan, Zhu Xun, Du Erxia, Yang Yuting, Wang Shaoli, Wu Qingjun, Zhang Youjun

机构信息

College of Agriculture, Yangtze University, Jingzhou 434025, China.

College of Life Science, Heilongjiang University, Harbin 150080, China.

出版信息

Int J Mol Sci. 2016 Jul 7;17(7):1034. doi: 10.3390/ijms17071034.

Abstract

The soil insect Bradysia odoriphaga (Diptera: Sciaridae) causes substantial damage to Chinese chive. Suitable reference genes in B. odoriphaga (Bradysia odoriphaga) have yet to be identified for normalizing target gene expression among samples by quantitative real-time PCR (qRT-PCR). This study was focused on identifying the expression stability of 12 candidate housekeeping genes in B. odoriphaga under various experiment conditions. The final stability ranking of 12 housekeeping genes was obtained with RefFinder, and the most suitable number of reference genes was analyzed by GeNorm. The results revealed that the most appropriate sets of internal controls were RPS15, RPL18, and RPS18 across developmental phases; RPS15, RPL28, and GAPDH across temperatures; RPS15 and RPL18 across pesticide treatments; RSP5, RPS18, and SDHA across photoperiods; ACTb, RPS18, and RPS15 across diets; RPS13 and RPL28 across populations; and RPS15, ACTb, and RPS18 across all samples. The use of the most suitable reference genes versus an arbitrarily selected reference gene resulted in significant differences in the analysis of a target gene expression. HSP23 in B. odoriphaga was found to be up-regulated under low temperatures. These results will contribute to the standardization of qRT-PCR and will also be valuable for further research on gene function in B. odoriphaga.

摘要

韭菜迟眼蕈蚊(双翅目:眼蕈蚊科)对韭菜造成了严重损害。目前尚未在韭菜迟眼蕈蚊中鉴定出合适的内参基因,用于通过定量实时荧光定量PCR(qRT-PCR)对样本间的靶基因表达进行标准化。本研究聚焦于鉴定12个候选管家基因在不同实验条件下在韭菜迟眼蕈蚊中的表达稳定性。使用RefFinder获得了12个管家基因的最终稳定性排名,并通过GeNorm分析了最合适的内参基因数量。结果表明,在不同发育阶段,最合适的内参基因组合是RPS15、RPL18和RPS18;在不同温度下是RPS15、RPL28和GAPDH;在不同农药处理下是RPS15和RPL18;在不同光周期下是RSP5、RPS18和SDHA;在不同食物条件下是ACTb、RPS18和RPS15;在不同种群间是RPS13和RPL28;在所有样本中是RPS15、ACTb和RPS18。使用最合适的内参基因与任意选择的内参基因相比,在靶基因表达分析中产生了显著差异。发现韭菜迟眼蕈蚊中的HSP23在低温下上调。这些结果将有助于qRT-PCR的标准化,也将为韭菜迟眼蕈蚊基因功能的进一步研究提供有价值的参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a5f/4964410/2002f1f5d073/ijms-17-01034-g001.jpg

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