College of Life Science and Technology, Southwest Miznu University, Chengdu, China.
Department of Molecular Genetics and Cell Biology, Maastricht University, Maastricht, The Netherlands.
PLoS One. 2018 Sep 26;13(9):e0204583. doi: 10.1371/journal.pone.0204583. eCollection 2018.
The intestinal mucosal development of piglets (Sus scrofa) during the weaning stage is important to their disease susceptibility and later growth. Quantitative real-time PCR (RT-qPCR) is commonly used to screen for differentially expressed genes and, for accurate results, proper reference housekeeping genes are essential. Here we assessed the mRNA expression of 18 well-known candidate reference genes at different parts of the gastrointestinal tract (GIT) of piglets during the weaning process by RT-qPCR assay. GeNorm analysis revealed that B2M/HMBS/HPRT1 were the three most stable reference genes and GAPDH was the least stable gene in the duodenum, jejunum, ileum, colon, and whole GIT. BestKeeper analysis found that B2M/HMBS/PGK11, HMBS/B2M/HPRT1, B2M/HMBS/HSPCB, B2M/HPRT1/HMBS, and B2M/HMBS/HPRT1 were the most stable genes in the duodenum, jejunum, ileum, colon, and whole GIT, respectively, whereas GAPDH, B-actin, and 18S rRNA were the least stable genes at different parts of the GIT. To confirm the crucial role of appropriate housekeeping genes in obtaining reliable results, we analyzed the expression of ALP using each of the 18 reference genes to normalize the RT-qPCR data. We found that the expression levels of ALP normalized using the most stable reference genes (B2M/HMBS/HPRT1) differed greatly from the expression levels obtained when the data were normalized using the least stable genes (GAPDH, B-actin, and 18S). We concluded that B2M/HMBS/HPRT1 were the optimal reference genes for gene expression analysis by RT-qPCR in the intestinal mucosal development stages of piglets at weaning. Our findings provide a set of porcine housekeeping reference genes for studies of mRNA expression in different parts of the pig intestine.
仔猪(Sus scrofa)断奶阶段的肠道黏膜发育对其疾病易感性和后期生长至关重要。实时定量 PCR(RT-qPCR)常用于筛选差异表达基因,为了获得准确的结果,适当的管家基因是必不可少的。本研究通过 RT-qPCR 检测,评估了断奶过程中仔猪胃肠道(GIT)不同部位 18 个已知候选管家基因的 mRNA 表达。GeNorm 分析显示,B2M/HMBS/HPRT1 是十二指肠、空肠、回肠、结肠和整个 GIT 中最稳定的 3 个参考基因,而 GAPDH 是最不稳定的基因。BestKeeper 分析发现,B2M/HMBS/PGK11、HMBS/B2M/HPRT1、B2M/HMBS/HSPCB、B2M/HPRT1/HMBS 和 B2M/HMBS/HPRT1 是十二指肠、空肠、回肠、结肠和整个 GIT 中最稳定的基因,而 GAPDH、B-actin 和 18S rRNA 是 GIT 不同部位最不稳定的基因。为了确认合适管家基因在获得可靠结果方面的关键作用,我们使用 18 个参考基因中的每一个基因分析了 ALP 的表达,以对 RT-qPCR 数据进行归一化。我们发现,使用最稳定的参考基因(B2M/HMBS/HPRT1)归一化的 ALP 表达水平与使用最不稳定的基因(GAPDH、B-actin 和 18S)归一化的表达水平有很大差异。我们得出结论,B2M/HMBS/HPRT1 是仔猪断奶后肠道黏膜发育阶段 RT-qPCR 基因表达分析的最佳参考基因。本研究为研究猪肠道不同部位的 mRNA 表达提供了一套猪管家基因参考。