Ojano-Dirain C, Toyomizu M, Wing T, Cooper M, Bottje W G
Department of Poultry Science, Center of Excellence for Poultry Science, University of Arkansas, Fayetteville, Arkansas 72701, USA.
Poult Sci. 2007 Feb;86(2):372-81. doi: 10.1093/ps/86.2.372.
This study was conducted to evaluate messenger RNA (mRNA) expression of genes that are involved in energy metabolism and mitochondrial biogenesis: avian adenine nucleotide translocator (avANT), cytochrome oxidase III (COX III), inducible nitric oxide synthase (iNOS), peroxisome proliferator-activated receptor-gamma (PPAR-gamma), avian PPAR-gamma coactivator-1alpha (avPGC-1alpha), and avian uncoupling protein in breast muscle and duodenum of broilers with low and high feed efficiency (FE). Total RNA was extracted from snap-frozen tissues from male broilers with low (0.55 +/- 0.01) and high (0.72 +/- 0.01) FE (n = 8 per group). Total RNA was reverse-transcribed using oligo(dT), random primers, or both followed by real-time reverse transcription-PCR. Protein oxidation, measured as protein carbonyls, was also evaluated in duodenal mucosa. Protein carbonyls were higher in low FE mucosa in tissue homogenate and mitochondrial fraction. The mRNA expression of iNOS and PPAR-gamma in the duodenum was lower in the low FE broilers, with no differences in avANT, COX III, and avPGC-1alpha. In contrast, expression of avANT and COX III mRNA in breast muscle was lower in low FE broilers with no differences in iNOS, PPAR-gamma, and avPGC-1alpha. The avian uncoupling protein in breast muscle was higher in low FE birds (P = 0.068). These results indicate that there are differences in the expression of mRNA encoding for mitochondrial transcription factors and proteins in breast muscle and duodenal tissue between low and high FE birds. The differences that were observed may also reflect inherent metabolic and gene regulation differences between tissues.
本研究旨在评估参与能量代谢和线粒体生物发生的基因的信使核糖核酸(mRNA)表达:禽腺嘌呤核苷酸转位酶(avANT)、细胞色素氧化酶III(COX III)、诱导型一氧化氮合酶(iNOS)、过氧化物酶体增殖物激活受体γ(PPAR-γ)、禽PPAR-γ共激活因子-1α(avPGC-1α)以及低饲料效率(FE)和高饲料效率的肉鸡胸肌和十二指肠中的禽解偶联蛋白。从低FE(0.55±0.01)和高FE(0.72±0.01)的雄性肉鸡的速冻组织中提取总RNA(每组n = 8)。使用寡聚(dT)、随机引物或两者进行总RNA反转录,随后进行实时逆转录PCR。还评估了十二指肠黏膜中以蛋白质羰基含量衡量的蛋白质氧化情况。在组织匀浆和线粒体部分中,低FE黏膜中的蛋白质羰基含量更高。低FE肉鸡十二指肠中iNOS和PPAR-γ的mRNA表达较低,而avANT、COX III和avPGC-1α没有差异。相比之下,低FE肉鸡胸肌中avANT和COX III mRNA的表达较低,而iNOS、PPAR-γ和avPGC-1α没有差异。低FE鸡的胸肌中的禽解偶联蛋白较高(P = 0.068)。这些结果表明,低FE和高FE鸡的胸肌和十二指肠组织中,编码线粒体转录因子和蛋白质的mRNA表达存在差异。观察到的差异也可能反映了组织之间固有的代谢和基因调控差异。