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

Herrera Vásquez, Ariel; Carvallo, Loreto; Blanco, Francisca; Tobar, Mariola; Villarroel Candia, Eva; Vicente Carbajosa, Jesus; Salinas, Paula y Holuigue, Loreto (2015). Transcriptional Control of Glutaredoxin GRXC9 Expression by a Salicylic Acid-Dependent and NPR1-Independent Pathway in Arabidopsis. "Plant Molecular Biology Reporter", v. 33 (n. 3); pp. 624-637. ISSN 0735-9640. https://doi.org/10.1007/s11105-014-0782-5.

Descripción

Título: Transcriptional Control of Glutaredoxin GRXC9 Expression by a Salicylic Acid-Dependent and NPR1-Independent Pathway in Arabidopsis
Autor/es:
  • Herrera Vásquez, Ariel
  • Carvallo, Loreto
  • Blanco, Francisca
  • Tobar, Mariola
  • Villarroel Candia, Eva
  • Vicente Carbajosa, Jesus
  • Salinas, Paula
  • Holuigue, Loreto
Tipo de Documento: Artículo
Título de Revista/Publicación: Plant Molecular Biology Reporter
Fecha: 2015
Volumen: 33
Materias:
Escuela: E.T.S.I. Agrónomos (UPM) [antigua denominación]
Departamento: Biotecnología - Biología Vegetal
Licencias Creative Commons: Reconocimiento - Sin obra derivada - No comercial

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Resumen

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.

Más información

ID de Registro: 41451
Identificador DC: http://oa.upm.es/41451/
Identificador OAI: oai:oa.upm.es:41451
Identificador DOI: 10.1007/s11105-014-0782-5
URL Oficial: http://link.springer.com/article/10.1007/s11105-014-0782-5
Depositado por: Memoria Investigacion
Depositado el: 12 Jul 2016 15:28
Ultima Modificación: 12 Jul 2016 15:28
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