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Blue light‐induced association of phototropin 2 with the Golgi apparatus
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Summary: Phototropins 1 and 2 (phot1 and phot2) function as blue light (BL) photoreceptors for phototropism, chloroplast relocation, stomatal opening and leaf flattening in Arabidopsis thaliana . Phototropin consists of two functional domains, the N‐terminal photosensory domain and the C‐terminal Ser/Thr kinase domain. However, little is known about the signal transduction pathway that links the photoreceptors and the physiological responses downstream of BL perception. To understand the mechanisms by which phot2 initiates these responses, we transformed the phot1phot2 double mutant of Arabidopsis with constructs encoding translationally fused phot2:green fluorescent protein (P2G). P2G was fully functional for the phot2‐specific physiological responses in these transgenic plants. It localized strongly to the plasma membrane and weakly to the cytoplasm in the dark. Upon illumination with BL, punctate P2G staining was formed within a few minutes in addition to the constitutive plasma membrane staining. This punctate distribution pattern matched well with that of the Golgi‐localized KAM1ΔC:mRFP. Brefeldin A (BFA), an inhibitor of vesicle trafficking, induced accumulation of P2G around the perinuclear region even in darkness, but the punctate pattern was not observed. After treatment of these cells with BL, P2G exhibited the punctate distribution pattern that matched with that of the Golgi marker. Hence, the light‐dependent association of P2G with the Golgi apparatus was BFA‐insensitive. A structure/function analysis indicated that the kinase domain was essential for the Golgi localization of phot2. The BL‐induced Golgi localization of phot2 may be one of important signaling steps in the phot2 signal transduction pathway.
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“Under blue light irradiation, part of the PHOT1 protein detaches from the cell membrane and disperses in the cytoplasm, in contrast, some PHOT2 proteins can be coupled to the Golgi apparatus (Sakamoto and Briggs, 2002; Kong et al., 2006; Wan et al., 2008).”
From The action of enhancing weak light capture via phototropic growth and chloroplast movement in plants (2022) · cites this paper as Kong et al., 2006
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“Although phot1 and phot2 do not possess a transmembrane domain, they localize to the inner side of the cytoplasmic membrane in the dark (Sakamoto and Briggs, 2002; Kong et al., 2006).”
From The action of enhancing weak light capture via phototropic growth and chloroplast movement in plants (2022) · cites this paper as Kong et al., 2006
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Cites
Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana
Clough, S. J., & Bent, A. F. (1998) · The Plant Journal · doi:10.1046/j.1365-313x.1998.00343.x · Cited by 22,014
GUS fusions: beta‐glucuronidase as a sensitive and versatile gene fusion marker in higher plants.
Jefferson, R., Kavanagh, T. A., & Bevan, M. W. (1987) · The EMBO Journal · doi:10.1002/j.1460-2075.1987.tb02730.x · Cited by 9,854
Lateral relocation of auxin efflux regulator PIN3 mediates tropism in Arabidopsis
Friml, J., Wiśniewska, J., Benková, E., Mendgen, K., & Palme, K. (2002) · Nature · doi:10.1038/415806a · Cited by 1,426
Auxin transport inhibitors block PIN1 cycling and vesicle trafficking
Geldner, N., Friml, J., Stierhof, Y.-D., Jürgens, G., & Palme, K. J. (2001) · Nature · doi:10.1038/35096571 · Cited by 1,244
Geldner, N., Anders, N., Wolters, H., Keicher, J., Kornberger, W., Müller, P., Delbarre, A., Ueda, T., Nakano, A., & Jürgens, G. (2003) · Cell · doi:10.1016/s0092-8674(03)00003-5 · Cited by 1,125
phot1 and phot2 mediate blue light regulation of stomatal opening
Kinoshita, T., Doi, M., Suetsugu, N., Kagawa, T., Wada, M., & Shimazaki, K.-I. (2001) · Nature · doi:10.1038/414656a · Cited by 899
Phototropins 1 and 2: versatile plant blue-light receptors
Briggs, W. R., & Christie, J. M. (2002) · Trends in Plant Science · doi:10.1016/s1360-1385(02)02245-8 · Cited by 785
Structural Basis of a Phototropin Light Switch
Harper, S. M., Neil, L. C., & Gardner, K. H. (2003) · Science · doi:10.1126/science.1086810 · Cited by 768
Auxin transport — shaping the plant
Friml, J. (2003) · Current Opinion in Plant Biology · doi:10.1016/s1369526602000031 · Cited by 739
Sakai, T., Kagawa, T., Kasahara, M., Swartz, T. E., Christie, J. M., Briggs, W. R., Wada, M., & Okada, K. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.101137598 · Cited by 715
Research works printed but not linked: 1
- Jarillo J.A., 1998, NPL1 (Accession number AF053941): a second member of the NPH serine/threonine kinase family of Arabidopsis, Plant Physiol., 117, 719
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Items 101–151 of 151
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Boex‐Fontvieille, E., Jossier, M., Davanture, M., Zivy, M., Hodges, M., & Tcherkez, G. G. B. (2014) · Plant Molecular Biology Reporter · doi:10.1007/s11105-014-0707-3 · Cited by 14
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Königer, M. (2013) · Advances in photosynthesis and respiration · doi:10.1007/978-94-007-6988-5_8 · Cited by 13
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Emmanuel Liscum, A. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.00827 · Cited by 13
Ishishita, K., Suetsugu, N., Hirose, Y., Higa, T., Doi, M., Wada, M., Matsushita, T., & Gotoh, E. (2016) · Journal of Plant Research · doi:10.1007/s10265-016-0790-7 · Cited by 14
Suzuki, H., Okamoto, A., Kojima, A., Nishimura, T., Takano, M., Kagawa, T., Kadota, A., Kanegae, T., & Koshiba, T. (2014) · Planta · doi:10.1007/s00425-014-2082-6 · Cited by 12
Hirano, S., Sasaki, K., Osaki, Y., Tahara, K., Takahashi, H., Takemiya, A., & Kodama, Y. (2022) · PNAS Nexus · doi:10.1093/pnasnexus/pgac030 · Cited by 13
Königer, M., Jessen, B., Yang, R., Sittler, D., & Harris, G. C. (2010) · Photosynthesis Research · doi:10.1007/s11120-010-9580-6 · Cited by 12
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Zhou, X., Zhu, T., Zhu, L., Luo, S., Deng, X., Lin, H., & Xi, D. (2016) · Journal of Plant Growth Regulation · doi:10.1007/s00344-016-9635-9 · Cited by 12
Photomorphogenesis and Photoperiodism in Plants
Weller, J. L., & Kendrick, R. E. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1468-5_19 · Cited by 11
Ikeda, H., Suzuki, T., Oka, Y., Gustafsson, A. L. S., Brochmann, C., Mochizuki, N., & Nagatani, A. (2021) · New Phytologist · doi:10.1111/nph.17381 · Cited by 10
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Zhang, Y., Liao, B., Li, F., Eneji, A. E., Du, M., & Tian, X. (2024) · Journal of Cotton Research · doi:10.1186/s42397-024-00170-5 · Cited by 8
Suzuki, T., Mioka, T., Tanaka, K., & Nagatani, A. (2020) · Scientific Reports · doi:10.1038/s41598-020-69459-0 · Cited by 8
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Kong, S., & Nagatani, A. (2008) · Plant Signaling & Behavior · doi:10.4161/psb.3.4.5239 · Cited by 7
Self-citationNoguchi, M., Noda, S., Matsubayashi, Y., & Kodama, Y. (2024) · The Plant Journal · doi:10.1111/tpj.17183 · Cited by 6
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Morrow, J., Willenburg, K. T., & Emmanuel Liscum, A. (2018) · Frontiers in Biology · doi:10.1007/s11515-018-1518-y · Cited by 6
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Mullen, J. L., & Kiss, J. Z. (2007) · Wiley eBooks · doi:10.1002/9780470388297.ch4 · Cited by 6
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Kim, J., Ahn, J., Bong, H., Wada, M., & Kong, S. (2020) · Journal of Plant Biology · doi:10.1007/s12374-020-09262-6 · Cited by 5
Self-citationUse of Confocal Laser as Light Source Reveals Stomata-Autonomous Function
Cañamero, R. C., Boccalandro, H. E., Casal, J. J., & Serna, L. (2006) · PLoS ONE · doi:10.1371/journal.pone.0000036 · Cited by 5
Kimura, Y., Kimura, I., & Kanegae, T. (2018) · Plant Signaling & Behavior · doi:10.1080/15592324.2018.1525995 · Cited by 5
Suetsugu, N., Takano, A., Kohda, D., & Wada, M. (2010) · Plant Signaling & Behavior · doi:10.4161/psb.5.12.13915 · Cited by 5
Light and temperature receptors and their convergence in plants
Song, J., Wu, W., & Hu, B. (2020) · Biologia Plantarum · doi:10.32615/bp.2019.104 · Cited by 4
Hormones and Light-Regulated Seedling Development
Yadukrishnan, P., Singh, D., Ravindran, N., Kushwaha, A. K., Job, N., Rahul, P. V., Yadav, A., Ramachandran, H., Bhagavatula, L., & Datta, S. (2021) · Plant in challenging environments · doi:10.1007/978-3-030-77477-6_4 · Cited by 4
Arabidopsis ARA4 modulates HY5 ‐mediated seedling growth and ABA responsiveness
Basu, R., Pal, A., & Chattopadhyay, S. (2025) · The Plant Journal · doi:10.1111/tpj.70260 · Cited by 3
Phosphorylation of WDR48 by phototropins drives starch degradation to promote stomatal opening
Yamauchi, S., Fuji, S., Ikuta, H., Sugiyama, N., Kodama, Y., Distefano, L., Fujii, H., Yamashita, K., Takase, H., Nomoto, M., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-70314-5 · Cited by 3
Light Sensing at the Plasma Membrane
Christie, J. M., Kaiserli, E., & Sullivan, S. (2010) · Plant cell monographs · doi:10.1007/978-3-642-13431-9_19 · Cited by 2
Secret Message at the Plant Surface
Boccalandro, H. E., Casal, J. J., & Serna, L. (2007) · Plant Signaling & Behavior · doi:10.4161/psb.2.5.4523 · Cited by 2
Kimura, I., & Kanegae, T. (2024) · Journal of Experimental Botany · doi:10.1093/jxb/erae003 · Cited by 2
Watanabe, E., Fekih, R., & Kasajima, I. (2019) · Signaling and communication in plants · doi:10.1007/978-3-319-95315-1_7 · Cited by 2
Guard-Cell-Specific Expression of Phototropin2 C-Terminal Fragment Enhances Leaf Transpiration
Riu, Y.-S., Song, H., Kim, H.-S., & Kong, S. (2021) · Plants · doi:10.3390/plants11010065 · Cited by 2
Self-citationPhototropin2 3’UTR overlaps with the AT5G58150 gene encoding an inactive RLK kinase
Łabuz, J., Banaś, A. K., Zgłobicki, P., Bażant, A., Sztatelman, O., Giza, A., Lasok, H., Prochwicz, A., Kozłowska-Mroczek, A., Jankowska, U., et al. (2024) · BMC Plant Biology · doi:10.1186/s12870-024-04732-2 · Cited by 2
Identification of photoperception and light signal transduction pathways in citrus
Quecini, V. (2007) · Genetics and Molecular Biology · doi:10.1590/s1415-47572007000500007 · Cited by 1
Regulation of Auxin Transport in Arabidopsis Leaf Vascular Development
Sherr, I. (2012) · doi:10.7939/r3db7vx42 · Cited by 1
Chup1 - a chloroplast movement protein and its interactions
Schmidt von Braun, S. (2008) · Elektronische Hochschulschriften der LMU München (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.8745 · Cited by 1
Deslous, P. (2018) · theses.fr (ABES) · doi:10.70675/01735f17z51cez4bf0zba24zc47edf4ac548 · Cited by 1
Celaya, R. B., Pedmale, U. V., & Liscum, E. (2009) · Signaling and communication in plants · doi:10.1007/978-3-540-89228-1_12 · Cited by 1
Multiple Wavelength Conversion for WDM Multicasting by Means of Non-Linear Effects in SOAs
Contestabile, G., Presi, M., & Ciaramella, E. (2006) · Kluwer Academic Publishers eBooks · doi:10.1007/0-387-23178-1_36
Light-regulated Development in Arabidopsis
Xu, D. (2014) · Gothenburg University Publications Electronic Archive (Gothenburg University)
Unraveling new roles and substrates for protein kinase CK2 in arabidopsis thaliana
Armengot, L. (2014) · TDX (Tesis Doctorals en Xarxa)
Mechanisms of the phototropic pathway
Morrow, J. (2018) · doi:10.32469/10355/69866
Xiang, Z., Qingping, Z., Xu, Y., Mu, S.-C., Xiao, Z., 赵, 翔., 赵, 青., 杨, 煦., 慕, 世., & 张, 骁. (2015) · Chinese Bulletin of Botany · doi:10.3724/sp.j.1259.2015.00122
Sakata, M., & Kodama, Y. (2020) · PLANT MORPHOLOGY · doi:10.5685/plmorphol.32.27
Liscum, E. (2009) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1165836.630216
Zhu, J., Zhou, F., Wang, Y., Liang, Y.-P., Qingping, Z., Han, Y., & Zhao, X. (2023) · The Crop Journal · doi:10.1016/j.cj.2023.04.007
Phototropin Mediates the Accurate Movement of Trifoliate Leaves in Medicago truncatula
Jiao, Z., Zhan, S., Liu, C., Zhang, H., Huang, W., Li, F., & Ge, L. (2025) · Plant Cell & Environment · doi:10.1111/pce.70025
Łabuz, J., Banaś, A. K., Zgłobicki, P., Bażant, A., Sztatelman, O., Giza, A., Lasok, H., Prochwicz, A., Kozłowska-Mroczek, A., Jankowska, U., et al. (2024) · Figshare · doi:10.6084/m9.figshare.25025998
Łabuz, J., Banaś, A. K., Zgłobicki, P., Bażant, A., Sztatelman, O., Giza, A., Lasok, H., Prochwicz, A., Kozłowska-Mroczek, A., Jankowska, U., et al. (2024) · Figshare · doi:10.6084/m9.figshare.25025909
Metadata
- Authors
- Kong, S., Suzuki, T., Tamura, K., Mochizuki, N., Hara‐Nishimura, I., & Nagatani, A.
- Affiliations
- Kyoto University (JP)
- Corresponding author
- Nagatani, Akira
- ORCID
- Venue
- The Plant Journal
- Publisher
- Wiley
- Published
- 2006-02-17
- Volume
- 45
- Issue
- 6
- Pages
- 994-1005
- ISSN
- 0960-7412 (ISSN-L)
- 1365-313X
- OpenAlex
- W2049111667
- Cited by
- 152
- References
- 50
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 6 · 2023: 1 · 2022: 7 · 2021: 7 · 2020: 8 · 2019: 4 · 2018: 7 · 2017: 1 · 2016: 10 · 2015: 9 · 2014: 14 · 2013: 10 · 2012: 14
- FWCI
- 12.31
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- The Plant Journal (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Japan Society for the Promotion of Science (13440239)
- 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 › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Photosynthetic Processes and Mechanisms
- Keywords
- phototropin 2, blue-light photoreceptor, Golgi apparatus, Golgi localization, phototropism, signal transduction, kinase domain, plasma membrane, vesicle trafficking, Arabidopsis thaliana, stomatal opening
- MeSH terms
- Cell Membrane, Cytoplasm, Golgi Apparatus, Light, Phosphoproteins, Recombinant Fusion Proteins, Immunoblotting, Signal Transduction, Protein Serine-Threonine Kinases, Arabidopsis, Protein Structure, Tertiary, Arabidopsis Proteins, Plants, Genetically Modified
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