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Modification of intracellular levels of glutathione‐dependent formaldehyde dehydrogenase alters glutathione homeostasis and root development
Author(s) -
ESPUNYA M. CARME,
DÍAZ MAYKELIS,
MORENOROMERO JORDI,
MARTÍNEZ M. CARMEN
Publication year - 2006
Publication title -
plant, cell and environment
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.646
H-Index - 200
eISSN - 1365-3040
pISSN - 0140-7791
DOI - 10.1111/j.1365-3040.2006.01497.x
Subject(s) - glutathione , formaldehyde dehydrogenase , biology , arabidopsis thaliana , biochemistry , intracellular , glutaredoxin , arabidopsis , microbiology and biotechnology , glutathione reductase , meristem , dehydrogenase , homeostasis , enzyme , mutant , gene , glutathione peroxidase
Glutathione (GSH)‐dependent formaldehyde dehydrogenase (FALDH) is a highly conserved medium‐chain dehydrogenase reductase and the main enzyme that metabolizes intracellular formaldehyde in eukaryotes. It has been recently shown that it exhibits a strong S ‐nitrosoglutathione (GSNO) reductase activity and could be a candidate to regulate NO‐signalling functions. However, there is a lack of knowledge about the tissue distribution of this enzyme in plants. Here, we have studied the localization and developmental expression of the enzyme using immunolocalization and histochemical activity assay methods. We conclude that FALDH is differentially expressed in the organs of Arabidopsis thaliana mature plants, with higher levels in roots and leaves from the first stages of development. Spatial distribution of FALDH in these two organs includes the main cell types [epidermis (Ep) and cortex (Cx) in roots, and mesophyll in leaves] and the vascular system. Arabidopsis thaliana mutants with modified levels of FALDH (both by over‐ and under‐expression of the FALDH‐encoding gene) show a significant reduction of root length, and this phenotype correlates with an overall decrease of intracellular GSH levels and alteration of spatial distribution of GSH in the root meristem. Transgenic roots are partially insensitive to exogenous GSH, suggesting an inability to detect reduction–oxidation (redox) changes of the GSH pool and/or maintain GSH homeostasis.