Structural and functional characterization of tree proteins involved in redox regulation: a new frontier in forest science

被引:1
作者
Jacquot, Jean-Pierre [1 ,2 ]
Couturier, Jeremy [1 ,2 ]
Didierjean, Claude [3 ,4 ]
Gelhaye, Eric [1 ,2 ]
Morel-Rouhier, Melanie [1 ,2 ]
Hecker, Arnaud [1 ,2 ]
Plomion, Christophe [5 ]
Guetle, Desiree D. [1 ,2 ,6 ,7 ]
Rouhier, Nicolas [1 ,2 ]
机构
[1] Univ Lorraine, Interact Arbres Microorganismes, UMR1136, F-54500 Vandoeuvre Les Nancy, France
[2] INRA, Interact Arbres Microorganismes, UMR1136, F-54280 Champenoux, France
[3] Univ Lorraine, CRM2, Equipe BioMod, UMR 7036,Fac Sci & Technol, BP 70239, F-54506 Vandoeuvre Les Nancy, France
[4] CNRS, CRM2, Equipe BioMod, UMR 7036,Fac Sci & Technol, BP 70239, F-54506 Vandoeuvre Les Nancy, France
[5] INRA, UMR1202, BIOGECO, F-33610 Cestas, France
[6] Univ Freiburg, Fac Biol, Plant Biotechnol, Schanzlestr 1, D-79104 Freiburg, Germany
[7] Univ Freiburg, Spemann Grad Sch Biol & Med SGBM, Albertstr 19A, D-79104 Freiburg, Germany
关键词
3D protein structure; Genome sequence; Glutaredoxin; Redox; Thioredoxin; Poplar; IRON-SULFUR CLUSTER; THIOREDOXIN-H; CRYSTAL-STRUCTURE; PEROXIREDOXIN-GLUTAREDOXIN; GLUTATHIONE PEROXIDASES; CATALYTIC MECHANISM; POPULUS-TRICHOCARPA; II PEROXIREDOXIN; GENOME SEQUENCE; REDUCED FORM;
D O I
10.1007/s13595-014-0442-9
中图分类号
S7 [林业];
学科分类号
0829 ; 0907 ;
摘要
Context Tree genomes are increasingly available with a large number of orphan genes coding for proteins, the function of which is still unknown. Aims and methods Modern techniques of genome analysis coupled with recombinant protein technology and massive 3D structural determination of tree proteins should help elucidate the function of many of the proteins encoded by orphan genes. X-ray crystallography and NMR will be the methods of choice for protein structure determination. Results In this review, we provide examples illustrating how the above-mentioned techniques improved our understanding of redox regulatory circuits in poplar, the first forest tree species sequenced. We showed that poplar peroxiredoxins use either thioredoxin or glutaredoxin as electron donors to reduce hydrogen peroxide. That glutaredoxin could be a reductant was unknown at the time of this discovery even in other biological organisms and was later confirmed notably by the observation that the two genes are fused in some bacteria and by the resolution of the structure of the bacterial hybrid protein. Similarly, genome analysis coupled to in vitro analysis of enzymatic properties led to the discovery that some plant methionine sulfoxide reductases can also use both thioredoxins and glutaredoxins as electron donors. Besides their disulfide reductase activity, it has been demonstrated that some poplar glutaredoxins are also involved in iron-sulfur center biogenesis and assembly. The original 3D structure determination has been made with poplar glutaredoxin C1 and then confirmed in a variety of other biological organisms including human. Our work also showed that in plants, so-called glutathione peroxidases use thioredoxins and not glutathione as electron donors. This is true for all non-selenocysteine-containing glutathione peroxidases. Finally, connections between the thioredoxin and glutaredoxin systems have been elucidated through the study of atypical poplar thioredoxins. Conclusions Altogether, these data illustrate how the combination of genetic engineering and structural biology improves our understanding of biological processes and helps fuel systems biology for trees and other biological species.
引用
收藏
页码:119 / 134
页数:16
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