Evaluation of reference genes for gene expression studies in pig muscle tissue by real-time PCR

被引:4
作者
Nesvadbova, M. [1 ]
Knoll, A. [1 ]
机构
[1] Mendel Univ Brno, Dept Anim Morphol Physiol & Genet, Zemedelska 1, Brno 61300, Czech Republic
关键词
gene stability; reference genes; quantitative PCR; Sus scrofa; age categories of pigs; muscle tissue; HOUSEKEEPING GENES; NORMALIZATION; SELECTION; QUANTIFICATION; QPCR;
D O I
10.17221/1428-CJAS
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
The selection of reference genes is essential for gene expression studies when using a real-time quantitative polymerase chain reaction (PCR). Reference gene selection should be performed for each experiment because the gene expression level may be changed in different experimental conditions. In this study, the stability of mRNA expression was determined for seven genes: HPRT1, RPS18, NACA, TBP, TAF4B, RPL32 and OAZ1. The stability of these reference genes was investigated in the skeletal muscle tissue of pig foetuses, piglets and adult pigs using real-time quantitative PCR and SYBR green chemistry. The expression of stability of the used reference genes was calculated using the geNorm application. Different gene expression profiles among the age categories of pigs were found out. RPS18 has been identified as the gene with the most stable expression in the muscle tissue of all pig age categories. HPRT1 and RPL32 were found to have the highest stability in piglets and adult pigs, and in foetuses and adults pigs, respectively. The newly used reference gene, TAF4B, reached the highest expression stability in piglets.
引用
收藏
页码:213 / 216
页数:4
相关论文
共 13 条
[1]   Selection of reference genes for normalisation of specific gene quantification data of Aspergillus niger [J].
Bohle, K. ;
Jungebloud, A. ;
Goecke, Y. ;
Dalpiaz, A. ;
Cordes, C. ;
Horn, H. ;
Hempel, D. C. .
JOURNAL OF BIOTECHNOLOGY, 2007, 132 (04) :353-358
[2]   Validation of housekeeping genes for normalizing RNA expression in real-time PCR [J].
Dheda, K ;
Huggett, JF ;
Bustin, SA ;
Johnson, MA ;
Rook, G ;
Zumla, A .
BIOTECHNIQUES, 2004, 37 (01) :112-+
[3]   Development of a new set of reference genes for normalization of real-time RT-PCR data of porcine backfat and Longissimus dorsi muscle, and evaluation with PPARGC1A [J].
Erkens, Tim ;
Van Poucke, Mario ;
Vandesompele, Jo ;
Goossens, Karen ;
Van Zeveren, Alex ;
Peelman, Luc J. .
BMC BIOTECHNOLOGY, 2006, 6 (1)
[4]   Maintenance of spermatogenesis requires TAF4b, a gonad-specific subunit of TFIID [J].
Falender, AE ;
Freiman, RN ;
Geles, KG ;
Lo, KC ;
Hwang, K ;
Lamb, DJ ;
Morris, PL ;
Tjian, R ;
Richards, JS .
GENES & DEVELOPMENT, 2005, 19 (07) :794-803
[5]   TAF4 inactivation in embryonic fibroblasts activates TGFβ signalling and autocrine growth [J].
Mengus, G ;
Fadloun, A ;
Kobi, D ;
Thibault, C ;
Perletti, L ;
Michel, I ;
Davidson, I .
EMBO JOURNAL, 2005, 24 (15) :2753-2767
[6]   Selection of reference genes for gene expression studies in pig tissues using SYBR green qPCR [J].
Nygard, Ann-Britt ;
Jorgensen, Claus B. ;
Cirera, Susanna ;
Fredholm, Merete .
BMC MOLECULAR BIOLOGY, 2007, 8
[7]   Development and application of multiple internal reference (housekeeper) gene assays for accurate normalisation of canine gene expression studies [J].
Peters, Iain R. ;
Peeters, Dominique ;
Helps, Chris R. ;
Day, Michael J. .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 2007, 117 (1-2) :55-66
[8]   Selecting control genes for RT-QPCR using public microarray data [J].
Popovici, Vlad ;
Goldstein, Darlene R. ;
Antonov, Janine ;
Jaggi, Rolf ;
Delorenzi, Mauro ;
Wirapati, Pratyaksha .
BMC BIOINFORMATICS, 2009, 10
[9]   Guideline to reference gene selection for quantitative real-time PCR [J].
Radonic, A ;
Thulke, S ;
Mackay, IM ;
Landt, O ;
Siegert, W ;
Nitsche, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 313 (04) :856-862
[10]   Verification of reference genes for relative quantification of gene expression by real-time reverse transcription PCR in the pig [J].
Svobodova, Katerina ;
Bilek, Karel ;
Knoll, Ales .
JOURNAL OF APPLIED GENETICS, 2008, 49 (03) :263-265