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Differential gene expression profile in ischemic myocardium of Wistar rats with acute myocardial infarction

机译:Wistar大鼠急性心肌梗死缺血心肌中的差异基因表达谱

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摘要

To determine the differential genes in ischemic myocardium of Wistar rats with acute myocardial infarction (AMI), we constructed two differential gene expression profiles. AMI model was generated by ligation of the left anterior descending coronary artery in Wistar rats. Total RNA was extracted from the normal and the ischemic heart tissues under the ligation point at the 8th day after the operation. Differential gene expression profiles of the two samples were constructed by using long serial analysis of gene expression (LongSAGE). Real time fluorescence quantitative PCR (Q-PCR) was used to confirm the expression changes of partial target genes. The main results were as follows: a total of 15966 tags were screened from the normal and the ischemic LongSAGE maps, and 9646 tags in the normal tissue and 9563 tags in the ischemic tissue were obtained. Among them, 7665 novel tags were identified by NCBI BLAST search. In the ischemic tissue, 142 genes significantly changed compared to those in the normal tissue (P < 0.05). These differentially expressed genes may play important roles in the pathways of oxidation and phosphorylation, ATP synthesis and glycolysis and so on. Partial genes identified by the LongSAGE were confirmed by Q-PCR. The results show that AMI causes a series of gene expression changes in the regulation of the pathways related to energy metabolism.
机译:为了确定Wistar大鼠急性心肌梗死(AMI)缺血性心肌中的差异基因,我们构建了两个差异基因表达谱。结扎Wistar大鼠左冠状动脉前降支,建立AMI模型。在手术后第8天,从结扎点的正常和缺血性心脏组织中提取总RNA。通过对基因表达进行长序列分析(LongSAGE),构建了两个样品的差异基因表达谱。实时荧光定量PCR(Q-PCR)用于确认部分靶基因的表达变化。主要结果如下:从正常和缺血的LongSAGE图谱中共筛选出15966个标签,在正常组织中获得了6466个标签,在缺血组织中获得了9563个标签。其中,通过NCBI BLAST检索鉴定出7665个新颖标签。在缺血组织中,与正常组织相比,有142个基因发生了显着变化(P <0.05)。这些差异表达的基因可能在氧化和磷酸化,ATP合成和糖酵解等途径中起重要作用。通过Q-PCR确认了LongSAGE鉴定出的部分基因。结果表明,AMI在与能量代谢有关的途径调控中引起一系列基因表达变化。

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