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Expression Pattern of Human Glutaredoxin 2 Isoforms: Identification and Characterization of Two Testis/Cancer Cell-Specific Isoforms

机译:人Glutaredoxin 2亚型的表达模式:两种睾丸/癌细胞特定亚型的鉴定和表征。

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摘要

The cellular redox state is associated with major cellular processes including differentiation, transformation, and apoptosis. Glutaredoxin 2 (Grx2) is a mitochondrial oxidoreductase suggested to play a critical role in protection against apoptotic stimuli. An alternative Grx2 transcript variant encoding a nonmitochondrial protein (Grx2b) was proposed before, but no data was available on the expression of this isoform. We have systematically investigated the expression of Grx2 transcript variants in human tissues and transformed cell lines. The transcript variant encoding mitochondrial Grx2 (Grx2a) was found to be ubiquitously expressed, emphasizing the general importance of the protein for mitochondrial redox homeostasis. In addition, we confirmed the previously suggested isoform Grx2b and identified a new third isoform (Grx2c) derived from alternative splicing of the Grx2b-encoding transcript. In normal tissue expression of both Grx2b and Grx2c was restricted to testes, but additionally we were able to demonstrate transcripts in various cancer cell lines. Both Grx2b and Grx2c are enzymatically active, but only Grx2c can complex the regulatory iron–sulfur cluster described for Grx2a. Expression of GFP fusion proteins suggested a cytosolic and nuclear localization of both Grx2b and Grx2c. Our findings provide the first evidence for functions of Grx2 outside mitochondria.
机译:细胞氧化还原状态与主要的细胞过程有关,包括分化,转化和凋亡。 Glutaredoxin 2(Grx2)是一种线粒体氧化还原酶,被认为在保护细胞免受凋亡刺激方面起着关键作用。以前曾提出过另一种编码非线粒体蛋白(Grx2b)的Grx2转录物变体,但该异构体的表达尚无数据。我们已经系统地研究了人类组织和转化细胞系中Grx2转录本变体的表达。发现编码线粒体Grx2(Grx2a)的转录本变体无处不在表达,强调了该蛋白对于线粒体氧化还原稳态的一般重要性。此外,我们证实了以前建议的同工型Grx2b,并确定了一个新的第三同工型(Grx2c),该新的第三同工型来自Grx2b编码转录本的可变剪接。在正常组织中,Grx2b和Grx2c的表达都限于睾丸,但除此之外,我们能够在各种癌细胞系中显示转录本。 Grx2b和Grx2c都具有酶活性,但是只有Grx2c才能使针对Grx2a所述的调节性铁硫簇络合。 GFP融合蛋白的表达暗示了Grx2b和Grx2c的胞质和核定位。我们的发现为线粒体外部Grx2的功能提供了第一个证据。

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  • 来源
    《Antioxidants & Redox Signaling》 |2008年第3期|p.547-558|共12页
  • 作者单位

    Maria Elisabet Lönn The Medical Nobel Institute for Biochemistry, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.Christoph Hudemann The Medical Nobel Institute for Biochemistry, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.Carsten Berndt The Medical Nobel Institute for Biochemistry, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.The Institute for Clinical Cytobiology and Cytopathology, Philipps University, Marburg, Germany.Valeria Cherkasov The Institute for Clinical Cytobiology and Cytopathology, Philipps University, Marburg, Germany.Francisco Capani The Department of Cell Biology and Histology, School of Medicine, University of Buenos Aires, Buenos Aires, Argentina.Arne Holmgren The Medical Nobel Institute for Biochemistry, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.Christopher Horst Lillig The Medical Nobel Institute for Biochemistry, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.The Institute for Clinical Cytobiology and Cytopathology, Philipps University, Marburg, Germany.;

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  • 正文语种 eng
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  • 关键词

    Glutaredoxin 2 (Grx2); Grx2b; Grx2a; Grx2c; Cancer Cell;

    机译:Glutaredoxin 2(Grx2);Grx2b;Grx2a;Grx2c;癌细胞;

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