Hydrogen Cyanamide Causes Reversible G2/M Cell Cycle Arrest Accompanied by Oxidation of the Nucleus and Cytosol

Author:

Velappan Yazhini1,de Simone Ambra2,Signorelli Santiago3ORCID,Considine John A.1,Foyer Christine H.4ORCID,Considine Michael J.15ORCID

Affiliation:

1. The UWA Institute of Agriculture, The University of Western Australia, Perth, WA 6009, Australia

2. Centre for Plant Sciences, Faculty of Biology, University of Leeds, Leeds LS2 9JT, UK

3. Food and Plant Biology Group, Departamento de Biología Vegetal, Facultad de Agronomía, Universidad de la República, Sayago CP 12900, Uruguay

4. School of Biosciences, College of Life and Environmental Sciences, University of Birmingham, Edgbaston B15 2TT, UK

5. Horticulture and Irrigated Agriculture, Department of Primary Industries and Regional Development, South Perth, WA 6151, Australia

Abstract

Hydrogen cyanamide (HC) has been widely used in horticulture to trigger bud burst following dormancy. Its use has been banned in some countries due to human health concerns, however the search for effective safe alternatives is delayed by lack of knowledge of the mechanism of HC action. Earlier studies demonstrate that HC stimulates the production of reactive oxygen species (ROS) and alters the rate of cell division. However, the relationships between HC effects on ROS, redox (reduction/oxidation) homeostasis and cell division are unknown. This study used Arabidopsis thaliana ((L.) Heynh.) seedlings expressing the redox reporter roGFP2 to measure the oxidation states of the nuclei and cytosol in response to HC treatment. The Cytrap dual cell cycle phase marker system and flow cytometry were used to study associated changes in cell proliferation. HC (1.5 mM) reversibly inhibited root growth during a 24 h treatment. Higher concentrations were not reversible. HC did not synchronise the cell cycle, in contrast to hydroxyurea. Rather, HC caused a gradual accumulation of cells in the G2/M phase and decline of G1/S phase cells, 16 to 24 h post-treatment. This was accompanied by increased oxidation of both the nuclei and cytosol. Taken together, these findings show that HC impairs proliferation of embryonic root meristem cells in a reversible manner through restriction of G2/M transition accompanied by increased cellular oxidation.

Funder

Wine Australia and the OIV

EU project

Australian Research Council

the University, State and Commonwealth Governments

Publisher

MDPI AG

Subject

Cell Biology,Clinical Biochemistry,Molecular Biology,Biochemistry,Physiology

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