The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Specific checkpoints regulate plant cell cycle progression in response to oxidative stress
Open accessAbstract
Summary: The effects of oxidative stress on plant cell cycle progression were studied both in cell suspensions and in planta . Oxidative stress of variable severity was imposed by the addition of different concentrations of the methyl‐quinone, menadione, into the growth media. In cell suspensions, flow cytometry analyses demonstrated that low concentrations (20–50 μM) of menadione impaired the G1/S transition, slowed DNA replication, and delayed the entry into mitosis. Furthermore, cells in G1 were more sensitive to menadione‐mediated oxidative stress than cells in S phase. Cell cycle arrest was associated with an inhibition of the activity of cyclin‐dependent kinases, cell cycle gene expression, and a concomitant activation of stress genes. Menadione‐mediated oxidative stress was shown to have very similar effects on tobacco plants, suggesting that a general regulation mechanism takes place in plants. These results define an oxidative stress checkpoint pathway that modulates both the expression of the core cell cycle genes and oxidative defence genes. Redox sensing could be of key importance in controlling cell cycle progression in environmental stress conditions.
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DNA damage and oxygen radical toxicity
Imlay, J. A., & Linn, S. (1988) · Science · doi:10.1126/science.3287616 · Cited by 1,974
The p21 inhibitor of cyclin-dependent kinases controls DNA replication by interaction with PCNA
Waga, S., Hannon, G. J., Beach, D., & Stillman, B. (1994) · Nature · doi:10.1038/369574a0 · Cited by 1,655
Auxin-resistant mutants of Arabidopsis thaliana with an altered morphology
Estelle, M. A., & Somerville, C. (1987) · Molecular and General Genetics MGG · doi:10.1007/bf00333575 · Cited by 576
Cited by
Functional analysis of oxidative stress-activated mitogen-activated protein kinase cascade in plants
Kovtun, Y., Chiu, W.-L., Tena, G., & Sheen, J. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.6.2940 · Cited by 1,530
Zinc in Soils and Crop Nutrition
Sadeghzadeh, B., & Rengel, Z. (2011) · The Molecular and Physiological Basis of Nutrient Use Efficiency in Crops · doi:10.1002/9780470960707.ch16 · Cited by 1,246
Catalase function in plants: a focus on Arabidopsis mutants as stress-mimic models
Mhamdi, A., Queval, G., Chaouch, S., Vanderauwera, S., Van Breusegem, F., & Noctor, G. (2010) · Journal of Experimental Botany · doi:10.1093/jxb/erq282 · Cited by 989
Stress-induced morphogenic responses: growing out of trouble?
Potters, G., Pasternak, T. P., Guisez, Y., Palme, K. J., & Jansen, M. A. K. (2007) · Trends in Plant Science · doi:10.1016/j.tplants.2007.01.004 · Cited by 770
Reactive oxygen species in plant development
Mhamdi, A., & Van Breusegem, F. (2018) · Development · doi:10.1242/dev.164376 · Cited by 667
Metadata
- Authors
- Reichheld, J., Vernoux, T., Lardon, F., Van Montagu, M., & Inzé, D.
- Venue
- The Plant Journal
- Publisher
- Wiley
- Published
- 1999-03
- Volume
- 17
- Issue
- 6
- Pages
- 647-656
- ISSN
- 0960-7412 (ISSN-L)
- 1365-313X
- OpenAlex
- W2099431745
- Cited by
- 243
- References
- 3
- FWCI
- 17.49
- Type
- journal article
- Language
- en
- Open access
- bronze
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- Reichheld, J., Vernoux, T., Lardon, F., Van Montagu, M., & Inzé, D. (1999). Specific checkpoints regulate plant cell cycle progression in response to oxidative stress. The Plant Journal. https://doi.org/10.1046/j.1365-313x.1999.00413.x
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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