The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Sink regulation of photosynthesis
Open accessAbstract
The concept that photosynthetic flux is influenced by the accumulation of photo-assimilate persisted for 100 years before receiving any strong experimental support. Precise analysis of the mechanisms of photosynthetic responses to sink activity required the development of a battery of appropriate molecular techniques and has benefited from contemporary interest in the effects of elevated CO2 on photosynthesis. Photosynthesis is one of the most highly integrated and regulated metabolic processes to maximize the use of available light, to minimize the damaging effects of excess light and to optimize the use of limiting carbon and nitrogen resources. Hypotheses of feedback regulation must take account of this integration. In the short term, departure from homeostasis can lead to redox signals, which cause rapid changes in the transcription of genes encoding photosystems I and II. End-product synthesis can exert short-term metabolic feedback control through Pi recycling. Beyond this, carbohydrate accumulation in leaves when there is an imbalance between source and sink at the whole plant level can lead to decreased expression of photosynthetic genes and accelerated leaf senescence. In a high CO2 world this may become a more prevalent feature of photosynthetic regulation. However, sink regulation of photosynthesis is highly dependent on the physiology of the rest of the plant. This physiological state regulates photosynthesis through signal transduction pathways that co-ordinate the plant carbon : nitrogen balance, which match photosynthetic capacity to growth and storage capacity and underpin and can override the direct short-term controls of photosynthesis by light and CO2. Photosynthate supply and phytohormones, particularly cytokinins, interact with nitrogen supply to control the expression of photosynthesis genes, the development of leaves and the whole plant nitrogen distribution, which provides the dominant basis for sink regulation of photosynthesis.
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Cites
Normalizing mitochondrial superoxide production blocks three pathways of hyperglycaemic damage
Nishikawa, T., Edelstein, D., Du, X. L., Yamagishi, S.-I., Matsumura, T., Kaneda, Y., Yorek, M. A., Beebe, D., Oates, P. J., Hammes, H.-P., et al. (2000) · Nature · doi:10.1038/35008121 · Cited by 4,277
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Mechanisms of Salinity Tolerance
Munns, R., & Tester, M. (2008) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.59.032607.092911 · Cited by 13,792
Hogewoning, S. W., Trouwborst, G., Maljaars, H., Poorter, H., van Ieperen, W., & Harbinson, J. (2010) · Journal of Experimental Botany · doi:10.1093/jxb/erq132 · Cited by 957
Phloem loading and unloading of sugars and amino acids
LALONDE, S., TEGEDER, M., THRONE‐HOLST, M., FROMMER, W. B., & PATRICK, J. W. (2003) · Plant, Cell & Environment · doi:10.1046/j.1365-3040.2003.00847.x · Cited by 438
Rerouting Carbon Flux to Enhance Photosynthetic Productivity
Ducat, D. C., Avelar-Rivas, J. A., Way, J. C., & Silver, P. A. (2012) · Applied and Environmental Microbiology · doi:10.1128/aem.07901-11 · Cited by 362
Controlled levels of salicylic acid are required for optimal photosynthesis and redox homeostasis
Mateo, A. (2006) · Journal of Experimental Botany · doi:10.1093/jxb/erj196 · Cited by 369
Metadata
- Authors
- Paul, M. J., & Foyer, C. H.
- Venue
- Journal of Experimental Botany
- Publisher
- Oxford University Press (OUP)
- Published
- 2001-07-01
- Volume
- 52
- Issue
- 360
- Pages
- 1383-1400
- ISSN
- 0022-0957 (ISSN-L)
- 1460-2431
- OpenAlex
- W2154965090
- Cited by
- 1,222
- References
- 1
- FWCI
- 5.43
- Type
- journal article
- Language
- en
- Open access
- green
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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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