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聚胺代谢激活的转基因小鼠肝脏的蛋白质组分析。

Proteomic analysis of livers from a transgenic mouse line with activated polyamine catabolism.

机构信息

Department of Biotechnology and Molecular Medicine, A.I. Virtanen Institute for Molecular Sciences, University of Kuopio, P.O.Box 1627, 70211 Kuopio, Finland.

出版信息

Amino Acids. 2010 Feb;38(2):613-22. doi: 10.1007/s00726-009-0420-y. Epub 2009 Dec 10.

Abstract

We have generated a transgenic mouse line that over expresses the rate-controlling enzyme of the polyamine catabolism, spermidine/spermine N (1)-acetyltransferase, under the control of a heavy metal inducible promoter. This line is characterized by a notable increase in SSAT activity in liver, pancreas and kidneys and a moderate increase in the rest of the tissues. SSAT induction results in an enhanced polyamine catabolism manifested as a depletion of spermidine and spermine and an overaccumulation of putrescine in all tissues. To study how the activation of polyamine catabolism affects other metabolic pathways, protein expression pattern of the livers of transgenic animals was analyzed by two-dimensional polyacrylamide gel electrophoresis and mass spectrometry. A total of 23 proteins were shown to be differentially expressed in the transgenic from the wild-type animals. Many of the identified proteins showed expression patterns associated with polyamine catabolism activation. However, the expression pattern of other proteins, such as repression of GST pi and selenium-binding protein 2 and 60 kDa heat-shock protein, could be explained by the overexpression of peroxisome proliferator-activated receptor gamma co-activator 1alpha in response to depleted ATP pools. The activation of the latter proteins is thought to lead to the improved insulin sensitivity seen in the MT-SSAT animals.

摘要

我们已经构建了一个转基因小鼠品系,该品系在重金属诱导型启动子的控制下,过度表达多胺分解的限速酶——精脒/精胺 N(1)-乙酰转移酶。该品系的特征是肝脏、胰腺和肾脏中的 SSAT 活性显著增加,而其他组织中的活性则适度增加。SSAT 的诱导导致多胺分解代谢增强,表现为精脒和精胺的消耗以及所有组织中腐胺的过度积累。为了研究多胺分解代谢的激活如何影响其他代谢途径,我们通过二维聚丙烯酰胺凝胶电泳和质谱分析了转基因动物肝脏的蛋白质表达模式。结果显示,与野生型动物相比,转基因动物的肝脏中有 23 种蛋白质表达模式发生了差异。许多鉴定出的蛋白质表现出与多胺分解代谢激活相关的表达模式。然而,其他蛋白质(如 GST pi 和硒结合蛋白 2 和 60kDa 热休克蛋白的表达受到抑制)的表达模式可以通过过表达对 ATP 池耗竭有反应的过氧化物酶体增殖物激活受体γ共激活因子 1α来解释。这些蛋白质的激活被认为是导致 MT-SSAT 动物胰岛素敏感性提高的原因。

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