The DOI matches its Crossref record; 8 of the 8 references it cites were found in a registry or an index.
Redox Regulation of Plant Development
Open accessAbstract
SIGNIFICANCE: We provide a conceptual framework for the interactions between the cellular redox signaling hub and the phytohormone signaling network that controls plant growth and development to maximize plant productivity under stress-free situations, while limiting growth and altering development on exposure to stress. RECENT ADVANCES: Enhanced cellular oxidation plays a key role in the regulation of plant growth and stress responses. Oxidative signals or cycles of oxidation and reduction are crucial for the alleviation of dormancy and quiescence, activating the cell cycle and triggering genetic and epigenetic control that underpin growth and differentiation responses to changing environmental conditions. CRITICAL ISSUES: The redox signaling hub interfaces directly with the phytohormone network in the synergistic control of growth and its modulation in response to environmental stress, but a few components have been identified. Accumulating evidence points to a complex interplay of phytohormone and redox controls that operate at multiple levels. For simplicity, we focus here on redox-dependent processes that control root growth and development and bud burst. FUTURE DIRECTIONS: The multiple roles of reactive oxygen species in the control of plant growth and development have been identified, but increasing emphasis should now be placed on the functions of redox-regulated proteins, along with the central roles of reductants such as NAD(P)H, thioredoxins, glutathione, glutaredoxins, peroxiredoxins, ascorbate, and reduced ferredoxin in the regulation of the genetic and epigenetic factors that modulate the growth and vigor of crop plants, particularly within an agricultural context.
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Citations
Cites
Oxygen sensing by metazoans: the central role of the HIF hydroxylase pathway.
Kaelin, W. G., & Ratcliffe, P. J. (2008) · Molecular Cell · doi:10.1016/j.molcel.2008.04.009 · Cited by 3,251 · cited 2×
“Changes in gene expression in response to low pO2 are centrally mediated by the hypoxia-inducible factor 1 (HIF1) transcription factor [for a recent review, see Kaelin and Ratcliffe (95)].”
Strigolactone inhibition of shoot branching
Gomez-Roldan, V., Fermas, S., Brewer, P. B., Puech-Pagès, V., Dun, E. A., Pillot, J.-P., Letisse, F., Matusova, R., Danoun, S., Portais, J.-C., et al. (2008) · Nature · doi:10.1038/nature07271 · Cited by 2,281
Inhibition of shoot branching by new terpenoid plant hormones
Umehara, M., Hanada, A., Yoshida, S., Akiyama, K., Arite, T., Takeda-Kamiya, N., Magome, H., Kamiya, Y., Shirasu, K., Yoneyama, K., et al. (2008) · Nature · doi:10.1038/nature07272 · Cited by 2,105
Signal integration in the control of shoot branching
Domagalska, M. A., & Leyser, O. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3088 · Cited by 835
MAX1 and MAX2 control shoot lateral branching in Arabidopsis
Stirnberg, P., van de Sande, K., & Leyser, H. M. O. (2002) · Development · doi:10.1242/dev.129.5.1131 · Cited by 692
Strigolactones affect lateral root formation and root-hair elongation in Arabidopsis
Kapulnik, Y., Delaux, P.-M., Resnick, N., Mayzlish-Gati, E., Wininger, S., Bhattacharya, C., Séjalon-Delmas, N., Combier, J.-P., Bécard, G., Belausov, E., et al. (2011) · Planta · doi:10.1007/s00425-010-1310-y · Cited by 502 · cited 1×
“SLs function downstream of auxin for the control of shoot (72, 179) and root branching (97, 98, 151).”
MAX2 participates in an SCF complex which acts locally at the node to suppress shoot branching
Stirnberg, P., Furner, I. J., & Ottoline Leyser, H. M. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03032.x · Cited by 429
Waters, M. T., Brewer, P. B., Bussell, J. D., Smith, S. M., & Beveridge, C. A. (2012) · Plant Physiology · doi:10.1104/pp.112.196253 · Cited by 232
Cited by
Reactive oxygen species in plant development
Mhamdi, A., & Van Breusegem, F. (2018) · Development · doi:10.1242/dev.164376 · Cited by 667
Ethylene: A Master Regulator of Salinity Stress Tolerance in Plants
Riyazuddin, R., Verma, R., Singh, K., Nisha, N., Keisham, M., Bhati, K. K., Kim, S. T., & Gupta, R. (2020) · Biomolecules · doi:10.3390/biom10060959 · Cited by 267
Metadata
- Authors
- Considine, M. J., & Foyer, C. H.
- Venue
- Antioxidants & Redox Signaling
- Publisher
- SAGE Publications
- Published
- 2014-09-20
- Volume
- 21
- Issue
- 9
- Pages
- 1305-1326
- ISSN
- 1523-0864 (ISSN-L)
- 1557-7716
- OpenAlex
- W1981230427
- Cited by
- 295
- References
- 8
- FWCI
- 6.32
- Type
- journal article
- Language
- en
- Open access
- hybrid
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.