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绵羊中性粒细胞定量PCR研究中的内参基因选择

Reference gene selection for quantitative PCR studies in sheep neutrophils.

作者信息

Vorachek William R, Bobe Gerd, Hall Jean A

机构信息

Department of Biomedical Sciences, College of Veterinary Medicine, Oregon State University, Corvallis, OR 97331, USA.

出版信息

Int J Mol Sci. 2013 May 30;14(6):11484-95. doi: 10.3390/ijms140611484.

Abstract

Reference genes are essential for studying mRNA expression with quantitative PCR (qPCR). We investigated 11 potential neutrophil reference genes (RPL19, GAPDH, ACTB, B2M, HPRT, G6PD, TFRC, PGK1, YWHAZ, SDHA and GYPC) for sheep under disease conditions of foot rot (FR) and with or without Se supplementation. Initial screening was based on gene expression level (<28 Cq cycles) and variability (SD < 1.5 Cq cycles) and excluded TFRC, GYPC and HPRT from further analysis. Expression stability of the remaining genes was evaluated using four software programs: geNorm, NormFinder, BestKeeper and the comparative delta Cq method. The neutrophil reference genes, G6PD, YWHAZ, GAPDH, RPL19 and SDHA, consistently ranked among the top five most stable genes under these experimental conditions. The SDHA gene expression was not stable in FR-diseased sheep receiving Se treatment and, thus, cannot be recommended as a reference gene. The commonly used genes, PGK1, ACTB and B2M, were not reliable reference genes, underscoring the need to validate neutrophil reference genes under different experimental conditions. Multiple references genes rather than a single gene may provide more robust and reliable results. The best pair of reference genes was SDHA/G6PD in healthy sheep and GADPH/YWHAZ in FR-diseased sheep.

摘要

参考基因对于通过定量PCR(qPCR)研究mRNA表达至关重要。我们研究了11个潜在的绵羊中性粒细胞参考基因(RPL19、GAPDH、ACTB、B2M、HPRT、G6PD、TFRC、PGK1、YWHAZ、SDHA和GYPC),这些绵羊处于腐蹄病(FR)疾病状态,且有或没有补充硒。初步筛选基于基因表达水平(<28个Cq循环)和变异性(标准差<1.5个Cq循环),并将TFRC、GYPC和HPRT排除在进一步分析之外。使用四个软件程序评估其余基因的表达稳定性:geNorm、NormFinder、BestKeeper和比较ΔCq法。在这些实验条件下,中性粒细胞参考基因G6PD、YWHAZ、GAPDH、RPL19和SDHA一直位列最稳定的五个基因之中。在接受硒处理的患FR病绵羊中,SDHA基因表达不稳定,因此,不推荐将其作为参考基因。常用基因PGK1、ACTB和B2M不是可靠的参考基因,这突出了在不同实验条件下验证中性粒细胞参考基因的必要性。多个参考基因而非单个基因可能会提供更稳健、可靠的结果。健康绵羊中最佳的参考基因对是SDHA/G6PD,患FR病绵羊中是GADPH/YWHAZ。

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