Transcriptional Control of Glutaredoxin GRXC9 Expression by a Salicylic Acid-Dependent and NPR1-Independent Pathway in Arabidopsis

Salicylic acid (SA) is a key hormone that mediates gene transcriptional reprogramming in the context of the defense response to stress. GRXC9, coding for a CC-type glutaredoxin from Arabidopsis, is an SA-responsive gene induced early and transiently by an NPR1-independent pathway. Here, we address t...

Description complète

Détails bibliographiques
Publié dans:Plant molecular biology reporter. - 1998. - 33(2015) vom: 01., Seite 624-637
Auteur principal: Herrera-Vásquez, Ariel (Auteur)
Autres auteurs: Carvallo, Loreto, Blanco, Francisca, Tobar, Mariola, Villarroel-Candia, Eva, Vicente-Carbajosa, Jesús, Salinas, Paula, Holuigue, Loreto
Format: Article
Langue:English
Publié: 2015
Accès à la collection:Plant molecular biology reporter
Sujets:Journal Article Glutaredoxin GRXC9 (GRX480) NPR1-independent Salicylic acid TGA transcription factors as-1-like element
LEADER 01000caa a22002652 4500
001 NLM255832443
003 DE-627
005 20250219120657.0
007 tu
008 231224s2015 xx ||||| 00| ||eng c
028 5 2 |a pubmed25n0852.xml 
035 |a (DE-627)NLM255832443 
035 |a (NLM)26696694 
040 |a DE-627  |b ger  |c DE-627  |e rakwb 
041 |a eng 
100 1 |a Herrera-Vásquez, Ariel  |e verfasserin  |4 aut 
245 1 0 |a Transcriptional Control of Glutaredoxin GRXC9 Expression by a Salicylic Acid-Dependent and NPR1-Independent Pathway in Arabidopsis 
264 1 |c 2015 
336 |a Text  |b txt  |2 rdacontent 
337 |a ohne Hilfsmittel zu benutzen  |b n  |2 rdamedia 
338 |a Band  |b nc  |2 rdacarrier 
500 |a Date Revised 01.10.2020 
500 |a published: Print-Electronic 
500 |a Citation Status PubMed-not-MEDLINE 
520 |a Salicylic acid (SA) is a key hormone that mediates gene transcriptional reprogramming in the context of the defense response to stress. GRXC9, coding for a CC-type glutaredoxin from Arabidopsis, is an SA-responsive gene induced early and transiently by an NPR1-independent pathway. Here, we address the mechanism involved in this SA-dependent pathway, using GRXC9 as a model gene. We first established that GRXC9 expression is induced by UVB exposure through this pathway, validating its activation in a physiological stress condition. GRXC9 promoter analyses indicate that SA controls gene transcription through two activating sequence-1 (as-1)-like elements located in its proximal region. TGA2 and TGA3, but not TGA1, are constitutively bound to this promoter region. Accordingly, the transient recruitment of RNA polymerase II to the GRXC9 promoter, as well as the transient accumulation of gene transcripts detected in SA-treated WT plants, was abolished in a knockout mutant for the TGA class II factors. We conclude that constitutive binding of TGA2 is essential for controlling GRXC9 expression, while binding of TGA3 in a lesser extent contributes to this regulation. Finally, overexpression of GRXC9 indicates that the GRXC9 protein negatively controls its own gene expression, forming part of the complex bound to the as-1-containing promoter region. These findings are integrated in a model that explains how SA controls transcription of GRXC9 in the context of the defense response to stress 
650 4 |a Journal Article 
650 4 |a Glutaredoxin GRXC9 (GRX480) 
650 4 |a NPR1-independent 
650 4 |a Salicylic acid 
650 4 |a TGA transcription factors 
650 4 |a as-1-like element 
700 1 |a Carvallo, Loreto  |e verfasserin  |4 aut 
700 1 |a Blanco, Francisca  |e verfasserin  |4 aut 
700 1 |a Tobar, Mariola  |e verfasserin  |4 aut 
700 1 |a Villarroel-Candia, Eva  |e verfasserin  |4 aut 
700 1 |a Vicente-Carbajosa, Jesús  |e verfasserin  |4 aut 
700 1 |a Salinas, Paula  |e verfasserin  |4 aut 
700 1 |a Holuigue, Loreto  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Plant molecular biology reporter  |d 1998  |g 33(2015) vom: 01., Seite 624-637  |w (DE-627)NLM098156438  |x 0735-9640  |7 nnns 
773 1 8 |g volume:33  |g year:2015  |g day:01  |g pages:624-637 
912 |a GBV_USEFLAG_A 
912 |a SYSFLAG_A 
912 |a GBV_NLM 
912 |a GBV_ILN_350 
951 |a AR 
952 |d 33  |j 2015  |b 01  |h 624-637