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The Rop GTPase Switch Controls Multiple Developmental Processes in Arabidopsis
Open accessAbstract
G proteins are universal molecular switches in eukaryotic signal transduction. The Arabidopsis genome sequence reveals no RAS small GTPase and only one or a few heterotrimeric G proteins, two predominant classes of signaling G proteins found in animals. In contrast, Arabidopsis possesses a unique family of 11 Rop GTPases that belong to the Rho family of small GTPases. Previous studies indicate that Rop controls actin-dependent pollen tube growth and H2O2-dependent defense responses. In this study, we tested the hypothesis that the Rop GTPase acts as a versatile molecular switch in signaling to multiple developmental processes in Arabidopsis. Immunolocalization using a general antibody against the Rop family proteins revealed a ubiquitous distribution of Rop proteins in all vegetative and reproductive tissues and cells in Arabidopsis. The cauliflower mosaic virus 35S promoter-directed expression of constitutively active GTP-bound rop2 (CA-rop2) and dominant negative GDP-bound rop2 (DN-rop2) mutant genes impacted many aspects of plant growth and development, including embryo development, seed dormancy, seedling development, lateral root initiation, morphogenesis of lateral organs in the shoot, shoot apical dominance and growth, phyllotaxis, and lateral organ orientation. The rop2 transgenic plants also displayed altered responses to the exogenous application of several hormones, such as abscisic acid-mediated seed dormancy, auxin-dependent lateral shoot initiation, and brassinolide-mediated hypocotyl elongation. CA-rop2 and DN-rop2expression had opposite effects on most of the affected processes, supporting a direct signaling role for Rop in regulating these processes. Based on these observations and previous results, we propose that Rop2 and other members of the Rop family participate in multiple distinct signaling pathways that control plant growth, development, and responses to the environment.
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Role 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
Li, H., Wu, G., Ware, D., Davis, K. R., & Yang, Z. (1998) · Plant Physiology · doi:10.1104/pp.118.2.407 · Cited by 194 · cited 13×
“Furthermore, Rop2 belongs to the largest Rop group (group IV) that includes Rop1 through Rop6 (Zheng and Yang, 2000).”
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Cited by
The Lateral Organ Boundaries Gene Defines a Novel, Plant-Specific Gene Family
Shuai, B., Reynaga-Peña, C. G., & Springer, P. S. (2002) · Plant Physiology · doi:10.1104/pp.010926 · Cited by 555
The Arabidopsis Rop2 GTPase Is a Positive Regulator of Both Root Hair Initiation and Tip Growth
Jones, M. A., Shen, J.-J., Fu, Y., Li, H., Yang, Z., & Grierson, C. S. (2002) · The Plant Cell · doi:10.1105/tpc.010359 · Cited by 437
Self-citationSmall GTPases: Versatile Signaling Switches in Plants
Yang, Z. (2002) · The Plant Cell · doi:10.1105/tpc.001065 · Cited by 428
Self-citationRopGAP4-Dependent Rop GTPase Rheostat Control of Arabidopsis Oxygen Deprivation Tolerance
Baxter-Burrell, A., Yang, Z., Springer, P. S., & Bailey-Serres, J. (2002) · Science · doi:10.1126/science.1071505 · Cited by 368
Self-citationDifferential TOR activation and cell proliferation in Arabidopsis root and shoot apexes
Li, X., Cai, W., Liu, Y., Li, H., Fu, L., Liu, Z., Xu, L., Liu, H., Xu, T., & Xiong, Y. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1618782114 · Cited by 316
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Metadata
- Authors
- Li, H., Shen, J.-J., Zheng, Z.-L., Lin, Y., & Yang, Z.
- Venue
- Plant Physiology
- Publisher
- Oxford University Press (OUP)
- Published
- 2001-06-01
- Volume
- 126
- Issue
- 2
- Pages
- 670-684
- ISSN
- 0032-0889 (ISSN-L)
- 1532-2548
- OpenAlex
- W2111624352
- Cited by
- 220
- References
- 3
- FWCI
- 19.87
- Type
- journal article
- Language
- en
- Open access
- bronze
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