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Muscle transcriptomic analyses in Angus cattle with divergent tenderness

机译:安格斯牛不同发情的肌肉转录组学分析

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Beef tenderness contributes significantly to variation of beef palatability, and is largely influenced by various genetic and environmental factors. To identify candidate genes and pathways related to beef tenderness, we analyzed the longissimus dorsi (LD) muscle of Angus cattle that had different degrees of tenderness, measured by Warner-Bratzler shear force (WBSF). Microarray and RT-PCR analyses identified 53 genes that were differentially expressed in LD samples categorized as either tough or tender, including myosin, heavy chain 3 skeletal muscle embryonic (MYH3), myosin heavy chain 8 skeletal muscle perinatal (MYH8), guanylate binding protein 5 (GBP5), fatty acid binding protein 4 (FABP4), Stearoyl-coenzyme A desaturase (SCD), Fatty acid synthase (FASN), ubiquitin-like with PHD and ring finger domains 1 (UHRF1). Most of these genes are involved in lipid metabolism and skeletal muscle contraction. Employing Gene ontology (GO) and Ingenuity Pathway Analysis (IPA), several GO terms and pathways were found to be related to hydrolase, peptidase and GTPase activity, lipid metabolism, small molecule biochemistry, molecular transport, and tissue development. Overall, this analysis provides insight into the metabolic relationships between muscle biology and beef quality.
机译:牛肉嫩度显着影响牛肉的适口性,并在很大程度上受各种遗传和环境因素的影响。为了确定与牛肉嫩度有关的候选基因和途径,我们分析了用华纳-布拉兹勒剪切力(WBSF)测量的具有不同嫩度的安格斯牛的背最长肌(LD)。芯片和RT-PCR分析鉴定了53种在LD样品中差异表达的基因,这些样品分为强韧或嫩,包括肌球蛋白,重链3骨骼肌胚胎(MYH3),肌球蛋白重链8骨骼肌围生期(MYH8),鸟苷酸结合蛋白5(GBP5),脂肪酸结合蛋白4(FABP4),硬脂酰辅酶A去饱和酶(SCD),脂肪酸合酶(FASN),具有PHD和无名指结构域1(UHRF1)的泛素样蛋白。这些基因中的大多数都参与脂质代谢和骨骼肌收缩。利用基因本体论(GO)和独创性途径分析(IPA),发现一些GO术语和途径与水解酶,肽酶和GTPase活性,脂质代谢,小分子生物化学,分子转运和组织发育有关。总体而言,该分析可深入了解肌肉生物学与牛肉品质之间的代谢关系。

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