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Inhibition of AtMYB2 DNA-binding by nitric oxide involves cysteine S-nitrosylation.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2007 Oct 05; Vol. 361 (4), pp. 1048-53. Date of Electronic Publication: 2007 Jul 31. - Publication Year :
- 2007
-
Abstract
- Nitric oxide (NO) can influence the transcriptional activity of a wide set of Arabidopsis genes. The aim of the present work was to investigate if NO modifies DNA-binding activity of AtMYB2 (a typical R2R3-MYB from Arabidopsis thaliana), by a posttranslational modification of its conserved Cys53 residue. We cloned a fully active minimal DNA-binding domain of AtMYB2 spanning residues 19-125, hereafter called M2D. In EMSA assays, M2D binds the core binding site 5'-[A]AACC[A]-3'. The NO donors SNP and GSNO inhibit M2D DNA-binding. As expected for a Cys S-nitrosylation, the NO-mediated inhibitory effect was reversed by DTT, and S-nitrosylation of Cys53 in M2D was detected by biotin switch assays. These results demonstrate that the DNA-binding of M2D is inhibited by S-nitrosylation of Cys53 as a consequence of NO action, thus establishing for the first time a relationship between the redox state and DNA-binding in a plant MYB transcription factor.
- Subjects :
- Arabidopsis Proteins metabolism
DNA metabolism
DNA-Binding Proteins chemistry
Nitric Oxide Donors pharmacology
Nitroprusside pharmacology
Oxidation-Reduction
Protein Processing, Post-Translational
S-Nitrosoglutathione pharmacology
Trans-Activators metabolism
Arabidopsis Proteins chemistry
Cysteine chemistry
Nitric Oxide chemistry
Trans-Activators chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 0006-291X
- Volume :
- 361
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 17686455
- Full Text :
- https://doi.org/10.1016/j.bbrc.2007.07.133