Dietz Karl-Josef, Jacob Simone, Oelze Marie-Luise, Laxa Miriam, Tognetti Vanesa, de Miranda Susana Marina Nunes, Baier Margarete, Finkemeier Iris
Biochemistry and Physiology of Plants, W5-134, Bielefeld University, D-33501 Bielefeld, Germany.
J Exp Bot. 2006;57(8):1697-709. doi: 10.1093/jxb/erj160. Epub 2006 Apr 10.
In 1996, cDNA sequences referred to as plant peroxiredoxins (Prx), i.e. a 1-Cys Prx and a 2-Cys Prx, were reported from barley. Ten years of research have advanced our understanding of plant Prx as thiol-based peroxide reductases with a broad substrate specificity, ranging from hydrogen peroxide to alkyl hydroperoxides and peroxinitrite. Prx have several features in common. (i) They are abundant proteins that are routinely detected in proteomics approaches. (ii) They interact with proteins such as glutaredoxins, thioredoxins, and cyclophilins as reductants, but also non-dithiol-disulphide exchange proteins. By work with transgenic plants, their activity was shown to (iii) affect metabolic integrity, (iv) protect DNA from damage in vitro and as shown here in vivo, and (v) modulate intracellular signalling related to reactive oxygen species and reactive nitrogen species. (vi) In all organisms Prx are encoded by small gene families that are of particular complexity in higher plants. A comparison of the Prx gene families in rice and Arabidopsis thaliana supports previous suggestions on Prx function in specific subcellular and metabolic context. (vii) Prx gene expression and activity are subjected to complex regulation realized by an integration of various signalling pathways. 2-Cys Prx expression depends on redox signals, abscisic acid, and protein kinase cascades. Besides these general properties, the chloroplast Prx have acquired specific roles in the context of photosynthesis. The thioredoxin-dependent peroxidase activity can be measured in crude plant extracts and contributes significantly to the overall H(2)O(2) detoxification capacity. Thus organellar Prx proteins enable an alternative water-water cycle for detoxification of photochemically produced H(2)O(2), which acts independently from the ascorbate-dependent Asada-Halliwell-Foyer cycle. 2-Cys Prx and Prx Q associate with thylakoid membrane components. The mitochondrial PrxII F is essential for root growth under stress. Following a more general introduction, the paper summarizes present knowledge on plant organellar Prx, addressing Prx in signalling, and also suggests some lines for future research.
1996年,从大麦中报道了被称为植物过氧化物氧还蛋白(Prx)的cDNA序列,即一种1-半胱氨酸Prx和一种2-半胱氨酸Prx。十年的研究使我们对植物Prx有了更深入的了解,它是一种基于硫醇的过氧化物还原酶,底物特异性广泛,从过氧化氢到烷基氢过氧化物和过氧亚硝酸盐。Prx有几个共同特征。(i)它们是丰富的蛋白质,在蛋白质组学方法中经常被检测到。(ii)它们与诸如谷氧还蛋白、硫氧还蛋白和亲环蛋白等蛋白质相互作用作为还原剂,也与非二硫醇-二硫化物交换蛋白相互作用。通过对转基因植物的研究,其活性被证明(iii)影响代谢完整性,(iv)在体外保护DNA免受损伤,以及如本文所示在体内保护DNA,(v)调节与活性氧和活性氮相关的细胞内信号传导。(vi)在所有生物体中,Prx由小基因家族编码,在高等植物中这些基因家族特别复杂。对水稻和拟南芥中Prx基因家族的比较支持了之前关于Prx在特定亚细胞和代谢环境中功能的推测。(vii)Prx基因表达和活性受到多种信号通路整合实现的复杂调控。2-半胱氨酸Prx的表达取决于氧化还原信号、脱落酸和蛋白激酶级联反应。除了这些一般特性外,叶绿体Prx在光合作用中还具有特定作用。硫氧还蛋白依赖性过氧化物酶活性可以在粗植物提取物中测量,并且对整体H₂O₂解毒能力有显著贡献。因此,细胞器Prx蛋白为光化学产生的H₂O₂解毒提供了一种替代的水-水循环,该循环独立于依赖抗坏血酸的阿萨达-哈利威尔-福耶循环。2-半胱氨酸Prx和Prx Q与类囊体膜成分相关联。线粒体PrxII F在胁迫下对根的生长至关重要。在进行了更一般性的介绍之后,本文总结了目前关于植物细胞器Prx的知识,讨论了Prx在信号传导方面的情况,并还提出了一些未来研究的方向。