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首页> 外文期刊>Livestock Science >Differentially expressed genes in skeletal muscle tissues from castrated Qinchuan cattle males compared with those from intact males.
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Differentially expressed genes in skeletal muscle tissues from castrated Qinchuan cattle males compared with those from intact males.

机译:与完整雄性相比,cattle割的秦川牛雄性骨骼肌组织中差异表达的基因。

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In order to study the molecular mechanism involved in meat quality differences especially tenderness variance caused by castration in Qinchuan cattle males, this study investigated the gene expression profile of longissimus thoracis (LT) muscle and screened differentially expressed genes in LT muscle from both intact male and castrated male Qinchuan cattle at 36 months of age utilising Bovine Genome Array. Significance Analysis of Microarrays (SAM) was used to identify the differentially expressed genes, Go (Gene Ontology) and pathway analyses were conducted on which by a free Web-based Molecular Annotation System 2.0 (MAS 2.0). Approximately 11 000 probe sets representing 10 000 genes were detected in LT muscle of 36-month-old Qinchuan cattle. After SAM analysis of the microarray data, 142 genes were shown to be differentially expressed. These genes were predominantly involved in collagen fibril organization and synthesis, regulation of cell growth and development and striated muscle contraction. The significant pathways involved mainly included ECM-receptor (extracellular matrix-receptor) interaction, cell communication and focal adhesion. Quantitative real-time PCR (qRT-PCR) was performed to validate some differentially expressed genes identified by microarray. These patterns of gene expression may contribute to understanding the molecular mechanism of better meat quality of beef derived from castrates than from intact males.
机译:为了研究秦川牛雄性meat割引起的肉质差异特别是嫩度差异所涉及的分子机制,本研究调查了 longissimus thoracis(LT)肌肉的基因表达谱,并筛选了差异表达基因。利用牛基因组阵列,从完整的雄性和去势雄性秦川牛在36个月大时获得的LT肌肉。微阵列的重要性分析(SAM)用于鉴定差异表达的基因Go(基因本体论),并通过免费的基于Web的分子注释系统2.0(MAS 2.0)进行了途径分析。在36个月大的秦川牛的LT肌肉中检测到约11000个代表10000个基因的探针组。对微阵列数据进行SAM分析后,显示142个基因差异表达。这些基因主要参与胶原纤维的组织和合成,细胞生长发育的调节和横纹肌收缩。涉及的重要途径主要包括ECM-受体(细胞外基质-受体)相互作用,细胞通讯和粘着斑。进行定量实时PCR(qRT-PCR)以验证通过微阵列鉴定的一些差异表达基因。这些基因表达模式可能有助于了解分子分子机制,使牛cast割后的牛肉品质比完整的公牛肉更好。

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