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Inhibition of AtMYB2 DNA-binding by nitric oxide involves cysteine S-nitrosylation.

Authors :
Serpa V
Vernal J
Lamattina L
Grotewold E
Cassia R
Terenzi H
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.

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