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Gene expression in breast muscle and duodenum from low and high feed efficient broilers

机译:低和高饲料高效肉鸡在胸肌和十二指肠中的基因表达

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摘要

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.
机译:进行这项研究以评估参与能量代谢和线粒体生物发生的基因的信使RNA(mRNA)表达:禽腺嘌呤核苷酸转运蛋白(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肉鸡的胸肌和十二指肠中的活化受体γ(PPAR-γ),禽类PPAR-γcoactivator-1alpha(avPGC-1alpha)和禽类解偶联蛋白,饲料效率高低。从雄性肉仔鸡的速冻组织中提取总RNA,其FE低(0.55 +/- 0.01)和FE高(0.72 +/- 0.01)(每组n = 8)。使用oligo(dT)和/或随机引物对总RNA进行逆转录,然后进行实时逆转录PCR。还测量了十二指肠粘膜中蛋白质羰基的蛋白质氧化。低FE粘膜组织匀浆和线粒体部分的羰基蛋白含量较高。低FE肉鸡十二指肠中iNOS和PPAR-γ的mRNA表达较低,而在vANT,COX III和avPGC-1alpha中没有差异。相比之下,在低FE肉鸡中,乳腺肌肉中avANT和COX III mRNA的表达较低,而iNOS,PPAR-γ和avPGC-1alpha没有差异。低FE鸟类的胸肌禽解偶联蛋白较高(P = 0.068)。这些结果表明,低FE和高FE鸟类之间在乳腺肌肉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组织之间固有的代谢和基因调控差异。

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