Biochemical and redox characterization of the mediator complex and its associated transcription factor GeBPL, a GLABROUS1 enhancer binding protein

被引:13
作者
Shaikhali, Jehad [1 ]
Davoine, Celine [1 ]
Brannstrom, Kristoffer [2 ]
Rouhier, Nicolas [3 ,4 ]
Bygdell, Joakim [1 ]
Bjorklund, Stefan [2 ]
Wingsle, Gunnar [1 ]
机构
[1] Swedish Univ Agr Sci SLU, Dept Forest Genet & Plant Physiol, Umea Plant Sci Ctr, S-90183 Umea, Sweden
[2] Umea Univ, Umea Plant Sci Ctr, Dept Med Biochem & Biophys, SE-90187 Umea, Sweden
[3] Univ Lorraine, Interact Arbres Microorganismes, UMR1136, F-54500 Vandoeuvre Les Nancy, France
[4] INRA, Interact Arbres Microorganismes, UMR1136, F-54280 Champenoux, France
基金
瑞典研究理事会;
关键词
Arabidopsis thaliana; CryR2; deoxyribonucleic acid (DNA)-binding; GLABROUS1 enhancer-binding protein (GeBP); mediator; redox; SYSTEMIC ACQUIRED-RESISTANCE; DEFENSE GENE-EXPRESSION; ARABIDOPSIS-THALIANA; DISEASE RESISTANCE; INTEGRATIVE HUB; SUBUNIT PFT1; DNA; THIOREDOXIN; ACTIVATION; YEAST;
D O I
10.1042/BJ20150132
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The eukaryotic mediator integrates regulatory signals from promoter-bound transcription factors (TFs) and transmits them to RNA polymerase II (Pol II) machinery. Although redox signalling is important in adjusting plant metabolism and development, nothing is known about a possible redox regulation of mediator. In the present study, using pull-down and yeast two-hybrid assays, we demonstrate the association of mediator (MED) subunits MED10a, MED28 and MED32 with the GLABROUS1 (GL1) enhancer-binding protein-like (GeBPL), a plant-specific TF that binds a promoter containing cryptochrome 1 response element 2 (CryR2) element. All the corresponding recombinant proteins form various types of covalent oligomers linked by intermolecular disulfide bonds that are reduced in vitro by the thioredoxin (TRX) and/or glutathione/glutaredoxin (GRX) systems. The presence of recombinant MED10a, MED28 and MED32 subunits or changes of its redox state affect the DNA-binding capacity of GeBPL suggesting that redox-driven conformational changes might modulate its activity. Overall, these results advance our understanding of how redox signalling affects transcription and identify mediator as a novel actor in redox signalling pathways, relaying or integrating redox changes in combinationwith specific TFs as GeBPL.
引用
收藏
页码:385 / 400
页数:16
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