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Plasma membrane aquaporins of the PIP1 and PIP2 subfamilies facilitate hydrogen peroxide diffusion into plant roots

BACKGROUND: The permeability of plasma membrane aquaporins (PIPs) to small solutes other than water greatly diversifies their potential functions in plant development and metabolic processes. One such process is stress signalling in which hydrogen peroxide (H(2)O(2)) plays a major role. Based on tra...

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Detalles Bibliográficos
Autores principales: Israel, David, Lee, Seong Hee, Robson, Thomas Matthew, Zwiazek, Janusz Jerzy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9721007/
https://www.ncbi.nlm.nih.gov/pubmed/36471241
http://dx.doi.org/10.1186/s12870-022-03962-6
Descripción
Sumario:BACKGROUND: The permeability of plasma membrane aquaporins (PIPs) to small solutes other than water greatly diversifies their potential functions in plant development and metabolic processes. One such process is stress signalling in which hydrogen peroxide (H(2)O(2)) plays a major role. Based on transport assays carried out in yeast, there are differences in the degree to which PIPs of Arabidopsis thaliana, are permeable to H(2)O(2) and thus they may differentially facilitate transmembrane diffusion. Here, we test whether specific PIPs aid in the transmembrane diffusion of H(2)O(2) to such an extent that knocking-out PIPs affects plant phenotype. We examined changes in growth and morphology, including biomass accumulation, root system architecture and relative water content, as well as gas exchange, across two H(2)O(2) treatments in knockout mutants of A. thaliana. RESULTS: We could infer that PIP-type aquaporins are permeable to H(2)O(2) in planta and that this permeability is physiologically relevant in a plant’s response to oxidative stress. In particular, the lack of functional PIP2;3 confers resistance to exogenously applied H(2)O(2) indicating that it facilitates H(2)O(2) entry into root cells. Additionally, PIP1;1 and PIP2;6 were found to facilitate H(2)O(2) diffusion, while PIP2;2 is required for proper root growth under controlled conditions. MAIN FINDINGS: We conclude that PIPs are physiologically relevant conduits for H(2)O(2) diffusion in the A. thaliana roots and participate in the regulation of stress responses. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-022-03962-6.