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Serial Expression Analysis of Liver Regeneration-Related Genes in Rat Regenerating Liver

机译:大鼠再生肝中肝脏再生相关基因的序列表达分析

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摘要

We investigated the gene expression changes in rat hepatic restoration with Rat Genome 230 2.0 chip containing 11,789 known genes and 13,231 unknown genes (taking up 90 percent of rat whole genome) following a 2/3 hepatectomy. The expression profiles and roles of these genes in rat liver regeneration (LR) were assayed using bioinformatics and systems biology method. Among the above genes, 1,004 known genes and 857 unknown genes were found to be associated with rat LR. The numbers of the known genes up-regulated, down-regulated, and up/down-regulated were 622, 443, and 15, respectively; that of the unknown genes were 367, 400, and 14, respectively. Out of the above two groups of genes, the ones up- and down-regulated 20 times or more were 62 and 38, 8, and 14, respectively. Notably, The highest expression level of dehydrogenase/reductase member 7 (DHRS7) was more than 968-fold compared to control, and alpha-1-B glycoprotein (A1BG), the product of gene with the lowest expression abundance, was 58 times lower than control. During rat liver regeneration, 467 up–regulated, 282 down–regulated, 10 up/down-regulated genes, and 1,031 undetected genes in our study interacted with each other and formed a network with a total of 4,014 connectivities. Among them, the genes for the regulation, synthesis, transport, signal transduction, protein modification, and physiological response formed 630, 290, 691, 373, 2010, and 20 connectivities, respectively; and the genes jun, fos, myc, ptgs2, ccna2, ccl2 had relatively higher degree of connectivity. The results indicated that cell apoptosis and inflammatory response were enhanced in the initial phase and the early part of progressive phase in LR.
机译:我们使用大鼠基因组230 2.0芯片研究了大鼠肝脏修复中的基因表达变化,该芯片包含11/789个已知基因和13,231个未知基因(占大鼠整个基因组的90%),在进行2/3肝切除术后。使用生物信息学和系统生物学方法测定了这些基因在大鼠肝再生(LR)中的表达谱和作用。在上述基因中,发现有1,004个已知基因和857个未知基因与大鼠LR相关。已知基因的上调,下调和上/下调数量分别为622、443和15。未知基因的分别是367、400和14。在上述两组基因中,上调或下调20次以上的基因分别为62和38、8和14。值得注意的是,脱氢酶/还原酶成员7(DHRS7)的最高表达水平是对照的968倍以上,表达丰度最低的基因产物α-1-B糖蛋白(A1BG)则降低了58倍。比控制。在大鼠肝再生过程中,我们研究中的467个上调基因,282个下调基因,10个上/下调基因和1,031个未检测到的基因相互影响,并形成了一个网络,共有4,014个连通性。其中,用于调节,合成,转运,信号转导,蛋白质修饰和生理应答的基因分别形成了630、290、691、373、2010和20个连通性。 jun,fos,myc,ptgs2,ccna2,ccl2基因具有较高的连通性。结果表明,在LR的初始阶段和进行阶段的早期,细胞凋亡和炎症反应增强。

著录项

  • 来源
    《Molecular Biotechnology》 |2009年第3期|221-231|共11页
  • 作者单位

    College of Fisheries Ocean University of China Qingdao Shandong Province 266100 China;

    The Laboratory of Toxicology College of Public Health Zhengzhou University Zhengzhou 450001 People’s Republic of China;

    College of Basic Medical Sciences Henan University of Traditional Chinese Medicine Zhengzhou 450008 China;

    School of Life Sciences Henan Agricultural University Zhengzhou 450002 China;

    The Laboratory of Toxicology College of Public Health Zhengzhou University Zhengzhou 450001 People’s Republic of China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Rat partial hepatectomy; Rat Genome 230 2.0 array; Genes associated with liver regeneration; Gene synergy;

    机译:大鼠部分肝切除术;大鼠基因组230 2.0阵列;与肝再生相关的基因;基因协同作用;

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