4.4 Article

Selection of Reference Genes for qRT-PCR in High Fat Diet-Induced Hepatic Steatosis Mice Model

期刊

MOLECULAR BIOTECHNOLOGY
卷 48, 期 3, 页码 255-262

出版社

HUMANA PRESS INC
DOI: 10.1007/s12033-010-9366-2

关键词

Hepatic steatosis; Gene expression; Quantitative real-time PCR; Housekeeping genes; Normalization

资金

  1. 973 Project [2006CB503904]
  2. 863 Project [2006 AA 02A409]
  3. National Natural Science Foundation of China [30725037, 30971077, 30971385]
  4. Shanghai Committee for Science and Technology [07JC14042]

向作者/读者索取更多资源

With the epidemic proportions of obesity worldwide and the concurrent prevalence of hepatic steatosis, there is an urgent need for better understanding the intrinsic mechanism of hepatic steatosis, especially the changes of gene expression underlying the development of hepatic steatosis and its associated abnormal liver function. Quantitative real-time PCR (qRT-PCR) is a sensitive and highly reproducible technique of gene expression analysis. However, for accurate and reliable gene expression results, it is vital to have an internal control gene expressed at constant levels under all the experimental conditions being analyzed for. In this study, the authors validated candidate reference genes suitable for qRT-PCR profiling experiments using livers from control mice and high fat diet-induced obese mice. Cross-validation of expression stability of ten selected reference genes using three popular algorithms, GeNorm, NormFinder, and BestKeeper found HPRT1 and GAPDH as most stable reference genes. Thus, HPRT1 and GAPDH are recommended as stable reference genes most suitable for gene expression studies in the development of hepatic steatosis.

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