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Expressed genes in regenerating rat liver after partial hepatectomy

机译:肝部分切除术后再生大鼠肝脏中表达的基因

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AIM: To reveal the liver regeneration (LR) and its control as well as the occurrence of liver disease and to study the gene expression profiles of 551 genes after partial hepatectomy (PH) in regenerating rat livers. METHODS: Five hundred and fifty-one expressed sequence tags screened by suppression subtractive hybridization were made into an in-house cDNA microarray, and the expressive genes and their expressive profiles in regenerating rat livers were analyzed by microarray and bioinformatics. RESULTS: Three hundred of the analyzed 551 genes were up- or downregulated more than twofolds at one or more time points during LR. Most of the genes were up- or downregulated 2-5 folds, but the highest reached 90 folds of the control. One hundred and thirty-nine of them showed upregulation, 135 displayed downregulation, and up or down expression of 26 genes revealed a dependence on regenerating livers. The genes expressed in 24-h regenerating livers were much more than those in the others. Cluster analysis and generalization analysis showed that there were at least six distinct temporal patterns of gene expression in the regenerating livers, that is, genes were expressed in the immediate early phase, early phase, intermediate phase, early-late phase, late phase, terminal phase. CONCLUSION: In LR, the number of down-regulated genes was almost similar to that of the upregulated genes; the successively altered genes were more than the rapidly transient genes. The temporal patterns of gene expression were similar 2 and 4 h, 12 and 16 h, 48 and 96 h, 72 and 144 h after PH. Microarray combined with suppressive subtractive hybridization can effectively identify the genes related to LR.
机译:目的:揭示肝再生(LR)及其控制以及肝病的发生,并研究再生肝大鼠部分肝切除(PH)后551个基因的基因表达谱。方法:将抑制消减杂交法筛选出的515个表达序列标签制成内部cDNA微阵列,并通过微阵列和生物信息学分析再生大鼠肝脏中的表达基因及其表达谱。结果:分析的551个基因中的300个在LR的一个或多个时间点上调或下调了两倍以上。大多数基因被上调或下调了2-5倍,但最高达到了对照的90倍。其中139个显示上调,135个显示下调,并且26个基因的上下表达表明对再生肝脏的依赖性。在24小时再生的肝脏中表达的基因比其他基因中的表达得多。聚类分析和泛化分析表明,再生肝中至少有六个不同的基因表达时间模式,即基因在早期,早期,中期,早期,晚期,晚期,末期表达相。结论:在LR中,下调基因的数量几乎与上调基因的数量相似;连续变化的基因比快速瞬时的基因更多。 PH后2小时和4小时,12小时和16小时,48小时和96小时,72小时和144小时,基因表达的时间模式相似。微阵列与抑制性消减杂交相结合可以有效地鉴定与LR相关的基因。

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