The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.
Predicting Essential Components of Signal Transduction Networks: A Dynamic Model of Guard Cell Abscisic Acid Signaling
Open accessAbstract
Plants both lose water and take in carbon dioxide through microscopic stomatal pores, each of which is regulated by a surrounding pair of guard cells. During drought, the plant hormone abscisic acid (ABA) inhibits stomatal opening and promotes stomatal closure, thereby promoting water conservation. Dozens of cellular components have been identified to function in ABA regulation of guard cell volume and thus of stomatal aperture, but a dynamic description is still not available for this complex process. Here we synthesize experimental results into a consistent guard cell signal transduction network for ABA-induced stomatal closure, and develop a dynamic model of this process. Our model captures the regulation of more than 40 identified network components, and accords well with previous experimental results at both the pathway and whole-cell physiological level. By simulating gene disruptions and pharmacological interventions we find that the network is robust against a significant fraction of possible perturbations. Our analysis reveals the novel predictions that the disruption of membrane depolarizability, anion efflux, actin cytoskeleton reorganization, cytosolic pH increase, the phosphatidic acid pathway, or K(+) efflux through slowly activating K(+) channels at the plasma membrane lead to the strongest reduction in ABA responsiveness. Initial experimental analysis assessing ABA-induced stomatal closure in the presence of cytosolic pH clamp imposed by the weak acid butyrate is consistent with model prediction. Simulations of stomatal response as derived from our model provide an efficient tool for the identification of candidate manipulations that have the best chance of conferring increased drought stress tolerance and for the prioritization of future wet bench analyses. Our method can be readily applied to other biological signaling networks to identify key regulatory components in systems where quantitative information is limited.
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Cites
Analysis of the genome sequence of the flowering plant Arabidopsis thaliana
Initiative, T. A. G. (2000) · Nature · doi:10.1038/35048692 · Cited by 9,301
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Kauffman, S. A. (1993) · doi:10.1093/oso/9780195079517.001.0001 · Cited by 7,855
A comprehensive analysis of protein–protein interactions in Saccharomyces cerevisiae
Uetz, P., Giot, L., Cagney, G., Mansfield, T. A., Judson, R. S., Knight, J. R., Lockshon, D., Narayan, V., Srinivasan, M., Pochart, P., et al. (2000) · Nature · doi:10.1038/35001009 · Cited by 4,706
Identification of a Plant Nitric Oxide Synthase Gene Involved in Hormonal Signaling
Guo, F.-Q., Okamoto, M., & Crawford, N. M. (2003) · Science · doi:10.1126/science.1086770 · Cited by 889
Interlinked Fast and Slow Positive Feedback Loops Drive Reliable Cell Decisions
Brandman, O., Ferrell, J. E., Li, R., & Meyer, T. (2005) · Science · doi:10.1126/science.1113834 · Cited by 466 · cited 2×
“Possibly, certain as-yetundiscovered interaction motifs, such as a synergistic feedforward loop [92] or dual positive feedback loops [93], could transform the Cac oscillation into a stable downstream output.”
BackgroundRole of Farnesyltransferase in ABA Regulation of Guard Cell Anion Channels and Plant Water Loss
Pei, Z.-M., Ghassemian, M., Kwak, C. M., McCourt, P., & Schroeder, J. I. (1998) · Science · doi:10.1126/science.282.5387.287 · Cited by 390
Cited by
The Language of Calcium Signaling
Dodd, A. N., Kudla, J., & Sanders, D. (2010) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-070109-104628 · Cited by 1,317
An overview of models of stomatal conductance at the leaf level
DAMOUR, G., SIMONNEAU, T., COCHARD, H., & URBAN, L. (2010) · Plant, Cell & Environment · doi:10.1111/j.1365-3040.2010.02181.x · Cited by 710
Zhang, Y., Zhu, H., Zhang, Q., Li, M., Yan, M., Wang, R., Wang, L., Welti, R., Zhang, W., & Wang, X. (2009) · The Plant Cell · doi:10.1105/tpc.108.062992 · Cited by 580
Plant xylem hydraulics: What we understand, current research, and future challenges
Venturas, M. D., Sperry, J. S., & Hacke, U. G. (2017) · Journal of Integrative Plant Biology · doi:10.1111/jipb.12534 · Cited by 487
Hirayama, T., & Shinozaki, K. (2007) · Trends in Plant Science · doi:10.1016/j.tplants.2007.06.013 · Cited by 494
Metadata
- Authors
- Li, S., Assmann, S. M., & Albert, R.
- Venue
- PLoS Biology
- Publisher
- Public Library of Science (PLoS)
- Published
- 2006-09-12
- Volume
- 4
- Issue
- 10
- Pages
- e312
- ISSN
- 1544-9173 (ISSN-L)
- 1545-7885
- OpenAlex
- W2014566660
- Cited by
- 418
- References
- 6
- FWCI
- 41.44
- Type
- journal article
- Language
- en
- Open access
- gold
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
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.