Use of Reference Gene Expression in Rat Distal Colon after Radiation Exposure: A Caveat
- 1 May 2004
- journal article
- Published by Radiation Research Society in Radiation Research
- Vol. 161 (5) , 597-602
- https://doi.org/10.1667/rr3173
Abstract
Research on the effects of ionizing radiation exposure includes transcriptome studies using real-time reverse transcription polymerase chain reaction (RT-PCR). These studies require the use of a reference gene that normalizes for cDNA quantity and corrects for transcription between different samples. In this study, several criteria are reviewed that allow the choice of a reference gene. With the example of five genes selected from the widely used standard housekeeping genes, Gapd (glyceraldehyde-3-phosphate dehydrogenase), Hprt (hypoxanthine-guanine phosphoribosyl transferase), cyclophilin A, AcRP0 (acidic ribosomal protein P0) and 18S, we show that the use of a reference gene without a preliminary study is hazardous. We have shown in rat colon after a hemi-body irradiation that expression of a gene of interest, the serotonin receptor type 1F (5-HT(1F)), was either increased or unchanged, with the result depending on the reference gene used. This work has led us to propose the use of two reference genes, a ribosomal gene, 18S, and another gene with a level of expression closer to that of the gene of interest. The methodology reported here may be applied to other studies of gene expression levels to evaluate the effects of experimental treatment on the expression of potential reference genes.Keywords
This publication has 15 references indexed in Scilit:
- Quantification of mRNA using real-time reverse transcription PCR (RT-PCR): trends and problemsJournal of Molecular Endocrinology, 2002
- Inflammatory and Anti-inflammatory Cytokines Regulate the Recovery from Sublethal X Irradiation in Rat ThymusRadiation Research, 2002
- Characterization of altered absorptive and secretory functions in the rat colon after abdominal irradiation: comparison with the effects of total-body irradiation.Radiation Research, 2002
- Validation of Endogenous Controls for Gene Expression Studies in Human Adipocytes and PreadipocytesHormone and Metabolic Research, 2001
- Direct Comparison of GAPDH, β-Actin, Cyclophilin, and 28S rRNA as Internal Standards for Quantifying RNA Levels under HypoxiaBiochemical and Biophysical Research Communications, 1999
- Development and Validation of Real-Time Quantitative Reverse Transcriptase–Polymerase Chain Reaction for Monitoring Gene Expression in Cardiac Myocytesin VitroAnalytical Biochemistry, 1999
- QUANTIFICATION OF MURINE CYTOKINE mRNAs USING REAL TIME QUANTITATIVE REVERSE TRANSCRIPTASE PCRCytokine, 1999
- Regulation of hypoxanthine phosphoribosyltransferase, glyceraldehyde‐3‐phosphate dehydrogenase and β‐actin mRNA expression in porcine immune cells and tissuesAnimal Biotechnology, 1998
- Effects of Fasting on the Expression of Gastrin, Cholecystokinin, and Somatostatin Genes and of Various Housekeeping Genes in the Pancreas and Upper Digestive Tract of RatsBiochemical and Biophysical Research Communications, 1997
- Quantitative comparison of mRNA levels in mammalian tissues: 28S ribosomal RNA level as an accurate internal controlNucleic Acids Research, 1989