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Arabidopsis NPH3: A NPH1 Photoreceptor-Interacting Protein Essential for Phototropism
Abstract
Phototropism of Arabidopsis thaliana seedlings in response to a blue light source is initiated by nonphototropic hypocotyl 1 (NPH1), a light-activated serine-threonine protein kinase. Mutations in three loci [ NPH2 , root phototropism 2 ( RPT2 ), and NPH3 ] disrupt early signaling occurring downstream of the NPH1 photoreceptor. The NPH3 gene, now cloned, encodes a NPH1-interacting protein. NPH3 is a member of a large protein family, apparently specific to higher plants, and may function as an adapter or scaffold protein to bring together the enzymatic components of a NPH1-activated phosphorelay.
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“Interaction screening revealed that NPH3, RPT2, and PKS1 interact with PHOT1 and participate in the regulation of hypocotyl phototropism (Motchoulski and Liscum, 1999; Harper et al., 2000; Inada et al., 2004).”
From The action of enhancing weak light capture via phototropic growth and chloroplast movement in plants (2022) · cites this paper as Motchoulski and Liscum, 1999
In the citing paper
“In the dark, NPH3 protein localizes to the cytoplasmic membrane and interacts with the N-terminus of the phot1 protein through its C-terminus (Motchoulski and Liscum, 1999).”
From The action of enhancing weak light capture via phototropic growth and chloroplast movement in plants (2022) · cites this paper as Motchoulski and Liscum, 1999
In the citing paper
“Mutations in NPH3 causes Arabidopsis lose all-intensity blue light-induced phototropism, indicating that NPH3 regulates both PHOT1-mediated phototropism under low-fluence blue light and the PHOT1- and PHOT2-mediated high-fluence blue light response (Liscum and Briggs, 1996; Motchoulski and Liscum, 1999).”
From The action of enhancing weak light capture via phototropic growth and chloroplast movement in plants (2022) · cites this paper as Motchoulski and Liscum, 1999
Citations
Cites
Molecular Cloning: A Laboratory Manual
Sambrook, J., Fritsch, E., & Maniatis, T. (1989) · UCLA - Biblioteca de Ciencias de la Salud · Cited by 133,589
Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
Altschul, S. (1997) · Nucleic Acids Research · doi:10.1093/nar/25.17.3389 · Cited by 73,302
Experiments in molecular genetics
Miller, J. H. (1972) · Medical Entomology and Zoology · Cited by 27,157
Predicting coiled coils from protein sequences.
Lupas, A., Van Dyke, M., & Stock, J. (1991) · Science · doi:10.1126/science.252.5009.1162 · Cited by 3,953
SMART, a simple modular architecture research tool: Identification of signaling domains
Schultz, J., Milpetz, F., Peer Bork, B., & Ponting, C. P. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.11.5857 · Cited by 3,577
Signaling Through Scaffold, Anchoring, and Adaptor Proteins
Pawson, T., & Scott, J. D. (1997) · Science · doi:10.1126/science.278.5346.2075 · Cited by 2,256
Kieber, J. J., Rothenberg, M., Roman, G., Feldmann, K. A., & Ecker, J. R. (1993) · Cell · doi:10.1016/0092-8674(93)90119-b · Cited by 1,923
Coiled coils: new structures and new functions
Lupas, A. N. (1996) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(96)10052-9 · Cited by 1,321
Assignment of 30 Microsatellite Loci to the Linkage Map of Arabidopsis
Bell, C. J., & Ecker, J. R. (1994) · Genomics · doi:10.1006/geno.1994.1023 · Cited by 1,016
Reed, J. W., Nagpal, P., Poole, D. S., Furuya, M., & Chory, J. (1993) · The Plant Cell · doi:10.1105/tpc.5.2.147 · Cited by 957
Flagged first, then by citations
Research works printed but not linked: 6
- Liscum E., Briggs W. R., Plant Cell 7, 473 (1995);
- K. Okada and Y. Shimura in Arabidopsis E. M. Meyerowitz and C. R. Somerville Eds. (Cold Spring Harbor Laboratory Press Plainview NY 1994) p. 665–684.
- The data are available at www.sciencemag.org/feature/data/1042358.shl.
- Albagli O., Dhordain P., DeWeindt C., LeCocq G., LePince D., Cell Growth Differ. 6, 1193 (1995);
- Choi S. D., Creelman R., Mullet J., Wing R. A.Weeds World2199517, .
- Reed J. W., Nagpal P., Poole D. S., Furuya M., Chory J., Plant Cell 5, 147 (1993).
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Chen, X., Lin, W., Wang, Y., Luan, S., & Xue, H. (2008) · The Plant Cell · doi:10.1105/tpc.107.052670 · Cited by 61
Liao, C., Yen, J.-H., & Wang, Y. (2008) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2008.07.025 · Cited by 60
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Li, Y., Dai, X., Cheng, Y., & Zhao, Y. (2010) · Molecular Plant · doi:10.1093/mp/ssq052 · Cited by 60
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Boccaccini, A., Legris, M., Krahmer, J., Petrolati, L. A., Goyal, A., Galván-Ampudia, C. S., Vernoux, T., Karayekov, E., Casal, J. J., & Fankhauser, C. (2020) · PLANT PHYSIOLOGY · doi:10.1104/pp.20.00243 · Cited by 46
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Tan, B., Lian, X., Cheng, J., Zeng, W., Zheng, X., Wang, W., Ye, X., Li, J., Li, Z., Zhang, L., et al. (2019) · BMC Genomics · doi:10.1186/s12864-019-6258-0 · Cited by 41
Xu, D., Gao, S., Ma, Y., Wang, X.-T., Feng, L., Li, L.-C., Xu, Z.-S., Chen, M., Chen, M., & Ma, Y.-Z. (2017) · Molecular Plant · doi:10.1016/j.molp.2017.08.004 · Cited by 40
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Ishishita, K., Higa, T., Tanaka, H., Inoue, S.-I., Chung, A., Ushijima, T., Matsushita, T., Kinoshita, T., Nakai, M., Wada, M., et al. (2020) · PLANT PHYSIOLOGY · doi:10.1104/pp.20.00059 · Cited by 34
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Zhao, X., Zhao, Q., Xu, C., Wang, J., Zhu, J., Shang, B., & Zhang, X. (2018) · Journal of Integrative Plant Biology · doi:10.1111/jipb.12639 · Cited by 32
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Zhao, Q., Zhu, J., Li, N., Wang, X., Zhao, X., & Zhang, X. (2020) · Journal of Integrative Plant Biology · doi:10.1111/jipb.12813 · Cited by 28
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Grauwe, L. D., Vriezen, W. H., Bertrand, S., Phillips, A. L., Vidal, A. M., Hedden, P., & Straeten, D. V. D. (2007) · Planta · doi:10.1007/s00425-007-0499-x · Cited by 24
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Ren, Y. N., Guo, S., Shu, S., Xu, Y., & Sun, J. (2017) · Scientia Horticulturae · doi:10.1016/j.scienta.2017.09.022 · Cited by 22
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de Wit, M., & Pierik, R. (2015) · Advances in photosynthesis and respiration · doi:10.1007/978-94-017-7291-4_6 · Cited by 23
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“In the dark, NPH3 protein localizes to the cytoplasmic membrane and interacts with the N-terminus of the phot1 protein through its C-terminus (Motchoulski and Liscum, 1999).”
BackgroundInfluential
Metadata
- Authors
- Motchoulski, A., & Liscum, E.
- Affiliations
- University of Missouri (US)
- Division of Biological Sciences, University of Missouri, Columbia, MO 65211, USA.
- Venue
- Science
- Published
- 1999-10-29
- Volume
- 286
- Issue
- 5441
- Pages
- 961-964
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2088376876
- Cited by
- 320
- References
- 37
- Citations by year
- 2026: 4 · 2025: 8 · 2024: 17 · 2023: 7 · 2022: 9 · 2021: 17 · 2020: 12 · 2019: 5 · 2018: 7 · 2017: 13 · 2016: 9 · 2015: 12 · 2014: 15 · 2013: 12 · 2012: 18
- FWCI
- 15.45
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Light effects on plants
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Molecular Biology Research
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Parasitism and Resistance
- Keywords
- NPH3, phototropism, blue light photoreception, serine/threonine kinase, phosphorelay, scaffold proteins, Rpt2, Arabidopsis thaliana
- MeSH terms
- Amino Acid Sequence, Cell Membrane, Cloning, Molecular, Escherichia coli, Molecular Sequence Data, Phosphoproteins, Plant Proteins, Protein Binding, Protein Serine-Threonine Kinases, Arabidopsis, Photoreceptor Cells, Invertebrate, Phototropism, Two-Hybrid System Techniques, Arabidopsis Proteins
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