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Monitoring of Chicken RNA Integrity as a Function of Prolonged Postmortem Duration

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 (pectorali...

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Autores principales: Malila, Yuwares, Srimarut, Yanee, U-chupaj, Juthawut, Strasburg, Gale, Visessanguan, Wonnop
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Asian-Australasian Association of Animal Production Societies (AAAP) and Korean Society of Animal Science and Technology (KSAST) 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4647106/
https://www.ncbi.nlm.nih.gov/pubmed/26580287
http://dx.doi.org/10.5713/ajas.15.0167
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author Malila, Yuwares
Srimarut, Yanee
U-chupaj, Juthawut
Strasburg, Gale
Visessanguan, Wonnop
author_facet Malila, Yuwares
Srimarut, Yanee
U-chupaj, Juthawut
Strasburg, Gale
Visessanguan, Wonnop
author_sort Malila, Yuwares
collection PubMed
description 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 A(260)/A(280) and A(260)/A(230) (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.
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spelling pubmed-46471062015-11-24 Monitoring of Chicken RNA Integrity as a Function of Prolonged Postmortem Duration Malila, Yuwares Srimarut, Yanee U-chupaj, Juthawut Strasburg, Gale Visessanguan, Wonnop Asian-Australas J Anim Sci Article 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 A(260)/A(280) and A(260)/A(230) (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. Asian-Australasian Association of Animal Production Societies (AAAP) and Korean Society of Animal Science and Technology (KSAST) 2015-11 /pmc/articles/PMC4647106/ /pubmed/26580287 http://dx.doi.org/10.5713/ajas.15.0167 Text en Copyright © 2015 by Asian-Australasian Journal of Animal Sciences
spellingShingle Article
Malila, Yuwares
Srimarut, Yanee
U-chupaj, Juthawut
Strasburg, Gale
Visessanguan, Wonnop
Monitoring of Chicken RNA Integrity as a Function of Prolonged Postmortem Duration
title Monitoring of Chicken RNA Integrity as a Function of Prolonged Postmortem Duration
title_full Monitoring of Chicken RNA Integrity as a Function of Prolonged Postmortem Duration
title_fullStr Monitoring of Chicken RNA Integrity as a Function of Prolonged Postmortem Duration
title_full_unstemmed Monitoring of Chicken RNA Integrity as a Function of Prolonged Postmortem Duration
title_short Monitoring of Chicken RNA Integrity as a Function of Prolonged Postmortem Duration
title_sort monitoring of chicken rna integrity as a function of prolonged postmortem duration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4647106/
https://www.ncbi.nlm.nih.gov/pubmed/26580287
http://dx.doi.org/10.5713/ajas.15.0167
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