Bai Qianfan, McGillivray Christine, da Costa Nuno, Dornan Saffron, Evans Gary, Stear Michael James, Chang Kin-Chow
Laboratory of Veterinary Molecular Medicine, Department of Veterinary Pathology, University of Glasgow, Bearsden Road, Glasgow G61 1QH, UK.
BMC Genomics. 2003 Mar 1;4(1):8. doi: 10.1186/1471-2164-4-8.
Microarray profiling has the potential to illuminate the molecular processes that govern the phenotypic characteristics of porcine skeletal muscles, such as hypertrophy or atrophy, and the expression of specific fibre types. This information is not only important for understanding basic muscle biology but also provides underpinning knowledge for enhancing the efficiency of livestock production.
We report on the de novo development of a composite skeletal muscle cDNA microarray, comprising 5500 clones from two developmentally distinct cDNA libraries (longissimus dorsi of a 50-day porcine foetus and the gastrocnemius of a 3-day-old pig). Clones selected for the microarray assembly were of low to moderate abundance, as indicated by colony hybridisation. We profiled the differential expression of genes between the psoas (red muscle) and the longissimus dorsi (white muscle), by co-hybridisation of Cy3 and Cy5 labelled cDNA derived from these two muscles. Results from seven microarray slides (replicates) correctly identified genes that were expected to be differentially expressed, as well as a number of novel candidate regulatory genes. Quantitative real-time RT-PCR on selected genes was used to confirm the results from the microarray.
We have developed a porcine skeletal muscle cDNA microarray and have identified a number of candidate genes that could be involved in muscle phenotype determination, including several members of the casein kinase 2 signalling pathway.
微阵列分析有潜力阐明调控猪骨骼肌表型特征(如肥大或萎缩)以及特定纤维类型表达的分子过程。这些信息不仅对理解基本肌肉生物学很重要,还为提高家畜生产效率提供了基础知识。
我们报告了一种复合骨骼肌cDNA微阵列的从头开发,该微阵列包含来自两个发育不同的cDNA文库(50日龄猪胎儿的背最长肌和3日龄仔猪的腓肠肌)的5500个克隆。如菌落杂交所示,为微阵列组装选择的克隆丰度低至中等。我们通过共杂交来自这两块肌肉的Cy3和Cy5标记的cDNA,分析了腰大肌(红色肌肉)和背最长肌(白色肌肉)之间基因的差异表达。七张微阵列玻片(重复样本)的结果正确地鉴定出了预期会差异表达的基因,以及一些新的候选调控基因。对选定基因进行定量实时RT-PCR以确认微阵列的结果。
我们开发了一种猪骨骼肌cDNA微阵列,并鉴定出了一些可能参与肌肉表型决定的候选基因,包括酪蛋白激酶2信号通路的几个成员。