Monitoring of Chicken RNA Integrity as a Function of Prolonged Postmortem Duration
Authors:
Open Access
- 3 September 2015
- journal article
- Published by Asian Australasian Association of Animal Production Societies in Asian-Australasian Journal of Animal Sciences
- Vol. 28 (11) , 1649-1656
Abstract
Gene expression profiling has offered new insights into postmortem molecular changes associated with meat quality. To acquire reliable transcript quantification, high quality RNA is required. The objective of this study was to analyze integrity of RNA isolated from chicken skeletal muscle (pectoralis major) and its capability of serving as the template in quantitative real-time polymerase chain reaction (qPCR) as a function of postmortem intervals representing the end-points of evisceration, carcass chilling and aging stages in chicken abattoirs. Chicken breast muscle was dissected from the carcasses (n = 6) immediately after evisceration, and one-third of each sample was instantly snap-frozen and labeled as 20 min postmortem. The remaining muscle was stored on ice until the next rounds of sample collection (1.5 h and 6 h postmortem). The delayed postmortem duration did not significantly affect A260/A280 and A260/A230 (p≥0.05), suggesting no altered purity of total RNA. Apart from a slight decrease in the 28s:18s ribosomal RNA ratio in 1.5 h samples (p<0.05), the value was not statistically different between 20 min and 6 h samples (p≥0.05), indicating intact total RNA up to 6 h. Abundance of reference genes encoding beta-actin (ACTB), glyceraldehyde 3-phosphate dehydrogenase (GAPDH), hypoxanthine-guanine phosphoribosyltransferase (HPRT), peptidylprolylisomerase A (PPIA) and TATA box-binding protein (TBP) as well as meat-quality associated genes (insulin-like growth factor 1 (IGF1), pyruvate dehydrogenase kinase isozyme 4 (PDK4), and peroxisome proliferator-activated receptor delta (PPARD) were investigated using qPCR. Transcript abundances of ACTB, GAPDH, HPRT, and PPIA were significantly different among all postmortem time points (p<0.05). Transcript levels of PDK4 and PPARD were significantly reduced in the 6 h samples (p<0.05). The findings suggest an adverse effect of a prolonged postmortem duration on reliability of transcript quantification in chicken skeletal muscle. For the best RNA quality, chicken skeletal muscle should be immediately collected after evisceration or within 20 min postmortem, and rapidly preserved by deep freezing.Keywords
This publication has 18 references indexed in Scilit:
- Highly efficient method for isolation of total RNA from adipose tissueBMC Research Notes, 2013
- Are one early muscle pH and one early temperature measurement sufficient to detect PSE breast meat in turkeys?British Poultry Science, 2011
- Evaluation of post mortem stability of porcine skeletal muscle RNAMeat Science, 2008
- Stability of RNA isolated from post-mortem tissues of Atlantic salmon (Salmo salar L.)Fish Physiology and Biochemistry, 2007
- Long-term stability of RNA in post-mortem bovine skeletal muscle, liver and subcutaneous adipose tissuesBMC Molecular Biology, 2007
- Understanding meat quality through the application of genomic and proteomic approachesMeat Science, 2006
- Genetic variability within and between breeds of poultry technological meat qualityWorld's Poultry Science Journal, 2004
- Transcriptional profile of postmortem skeletal musclePhysiological Genomics, 2004
- Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT MethodMethods, 2001
- BIOCHEMISTRY OF CHICKEN MUSCLE AS RELATED TO RIGOR MORTIS AND TENDERIZATION aJournal of Food Science, 1960