Cargando…

The AtCRK5 Protein Kinase Is Required to Maintain the ROS NO Balance Affecting the PIN2-Mediated Root Gravitropic Response in Arabidopsis

The Arabidopsis AtCRK5 protein kinase is involved in the establishment of the proper auxin gradient in many developmental processes. Among others, the Atcrk5-1 mutant was reported to exhibit a delayed gravitropic response via compromised PIN2-mediated auxin transport at the root tip. Here, we report...

Descripción completa

Detalles Bibliográficos
Autores principales: Cséplő, Ágnes, Zsigmond, Laura, Andrási, Norbert, Baba, Abu Imran, Labhane, Nitin M., Pető, Andrea, Kolbert, Zsuzsanna, Kovács, Hajnalka E., Steinbach, Gábor, Szabados, László, Fehér, Attila, Rigó, Gábor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8197844/
https://www.ncbi.nlm.nih.gov/pubmed/34205973
http://dx.doi.org/10.3390/ijms22115979
Descripción
Sumario:The Arabidopsis AtCRK5 protein kinase is involved in the establishment of the proper auxin gradient in many developmental processes. Among others, the Atcrk5-1 mutant was reported to exhibit a delayed gravitropic response via compromised PIN2-mediated auxin transport at the root tip. Here, we report that this phenotype correlates with lower superoxide anion (O(2)(•−)) and hydrogen peroxide (H(2)O(2)) levels but a higher nitric oxide (NO) content in the mutant root tips in comparison to the wild type (AtCol-0). The oxidative stress inducer paraquat (PQ) triggering formation of O(2)(•−) (and consequently, H(2)O(2)) was able to rescue the gravitropic response of Atcrk5-1 roots. The direct application of H(2)O(2) had the same effect. Under gravistimulation, correct auxin distribution was restored (at least partially) by PQ or H(2)O(2) treatment in the mutant root tips. In agreement, the redistribution of the PIN2 auxin efflux carrier was similar in the gravistimulated PQ-treated mutant and untreated wild type roots. It was also found that PQ-treatment decreased the endogenous NO level at the root tip to normal levels. Furthermore, the mutant phenotype could be reverted by direct manipulation of the endogenous NO level using an NO scavenger (cPTIO). The potential involvement of AtCRK5 protein kinase in the control of auxin-ROS-NO-PIN2-auxin regulatory loop is discussed.