Phytochrome A Regulates the Intracellular Distribution of Phototropin 1–Green Fluorescent Protein in Arabidopsis thaliana
Open accessAbstract
It has been known for decades that red light pretreatment has complex effects on subsequent phototropic sensitivity of etiolated seedlings. Here, we demonstrate that brief pulses of red light given 2 h prior to phototropic induction by low fluence rates of blue light prevent the blue light–induced loss of green fluorescent protein–tagged phototropin 1 (PHOT1-GFP) from the plasma membrane of cortical cells of transgenic seedlings of Arabidopsis thaliana expressing PHOT1-GFP in a phot1-5 null mutant background. This red light effect is mediated by phytochrome A and requires ∼2 h in the dark at room temperature to go to completion. It is fully far red reversible and shows escape from photoreversibility following 30 min of subsequent darkness. Red light–induced inhibition of blue light–inducible changes in the subcellular distribution of PHOT1-GFP is only observed in rapidly elongating regions of the hypocotyl. It is absent in hook tissues and in mature cells below the elongation zone. We hypothesize that red light–induced retention of the PHOT1-GFP on the plasma membrane may account for the red light–induced increase in phototropic sensitivity to low fluence rates of blue light.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Red light-activated phytochromes can inhibit blue light-induced migration of PHOT1 to the cytoplasm.
“Red light-activated phytochromes can inhibit blue light-induced migration of PHOT1 to the cytoplasm. (Rosler et al., 2007; Han et al., 2008).”
From The action of enhancing weak light capture via phototropic growth and chloroplast movement in plants (2022) · cites this paper as Han et al., 2008
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
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 · see citing works
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 · see citing works
Self-citationArabidopsis NPH1: A Protein Kinase with a Putative Redox-Sensing Domain
Huala, E., Oeller, P. W., Emmanuel Liscum, A., Han, I., Larsen, E., & Briggs, W. R. (1997) · Science · doi:10.1126/science.278.5346.2120 · Cited by 706 · see citing works
Self-citationPhytochrome A and Phytochrome B Have Overlapping but Distinct Functions in Arabidopsis Development
Reed, J. W., Nagatani, A., Elich, T. D., Fagan, M., & Chory, J. (1994) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.4.1139 · Cited by 673 · see citing works
Arabidopsis NPH1: A Flavoprotein with the Properties of a Photoreceptor for Phototropism
Christie, J. M., Reymond, P., Powell, G. K., Bernasconi, P., Raibekas, A. A., Emmanuel Liscum, A., & Briggs, W. R. (1998) · Science · doi:10.1126/science.282.5394.1698 · Cited by 589 · see citing works
Self-citationDecoding of Light Signals by Plant Phytochromes and Their Interacting Proteins
Bae, G., & Choi, G. (2008) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.59.032607.092859 · Cited by 492 · see citing works
Mutations in the NPH1 Locus of Arabidopsis Disrupt the Perception of Phototropic Stimuli
Emmanuel Liscum, A., & Briggs, W. R. (1995) · The Plant Cell · doi:10.1105/tpc.7.4.473 · Cited by 426 · see citing works
Self-citationPKS1, a Substrate Phosphorylated by Phytochrome That Modulates Light Signaling in Arabidopsis
Fankhauser, C., Yeh, K., Clark, J., Lagarias, J. C., Zhang, H., Elich, T. D., & Chory, J. (1999) · Science · doi:10.1126/science.284.5419.1539 · Cited by 409 · see citing works
Cellular and Subcellular Localization of Phototropin 1
Sakamoto, K., & Briggs, W. R. (2002) · The Plant Cell · doi:10.1105/tpc.003293 · Cited by 405 · see citing works
Self-citationPHYTOCHROME KINASE SUBSTRATE 1 is a phototropin 1 binding protein required for phototropism
Lariguet, P., Schepens, I., Hodgson, D., Pedmale, U. V., Trevisan, M., Kami, C., de Carbonnel, M., Alonso, J. M., Ecker, J. R., Liscum, E., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0603799103 · Cited by 190 · see citing works
Phytochrome Control of Two Low-Irradiance Responses in Etiolated Oat Seedlings
Mandoli, D. F., & Briggs, W. R. (1981) · PLANT PHYSIOLOGY · doi:10.1104/pp.67.4.733 · Cited by 176 · see citing works
Self-citationBlue light‐induced association of phototropin 2 with the Golgi apparatus
Kong, S., Suzuki, T., Tamura, K., Mochizuki, N., Hara‐Nishimura, I., & Nagatani, A. (2006) · The Plant Journal · doi:10.1111/j.1365-313x.2006.02667.x · Cited by 152 · see citing works
Phytochrome A Regulates Red-Light Induction of Phototropic Enhancement in Arabidopsis
Parks, B. M., Quail, P. H., & Hangarter, R. P. (1996) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.1.155 · Cited by 124 · see citing works
The Phototropic Responses of Higher Plants
Briggs, W. R. (1963) · Annual Review of Plant Physiology · doi:10.1146/annurev.pp.14.060163.001523 · Cited by 112 · see citing works
Self-citationWan, Y.-L., Eisinger, W., Ehrhardt, D., Kubitscheck, U., Baluska, F., & Briggs, W. (2008) · Molecular Plant · doi:10.1093/mp/ssm011 · Cited by 105 · see citing works
Self-citationPhototropic Dosage-Response Curves for Oat Coleoptiles
Zimmerman, B. K., & Briggs, W. R. (1963) · PLANT PHYSIOLOGY · doi:10.1104/pp.38.3.248 · Cited by 104 · see citing works
Self-citationMutants of Arabidopsis thaliana with altered phototropism
Khurana, J. P., & Poff, K. L. (1989) · Planta · doi:10.1007/bf00391868 · Cited by 102 · see citing works
Cho, H., Tseng, T., Kaiserli, E., Sullivan, S., Christie, J. M., & Briggs, W. R. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.106.089839 · Cited by 102 · see citing works
Self-citationJanoudi, A., Gordon, W. R., Wagner, D., Quail, P. H., & Poff, K. L. (1997) · PLANT PHYSIOLOGY · doi:10.1104/pp.113.3.975 · Cited by 87 · see citing works
Effect of Red Light on the Phototropic Sensitivity of Corn Coleoptiles
Chon, H. P., & Briggs, W. R. (1966) · PLANT PHYSIOLOGY · doi:10.1104/pp.41.10.1715 · Cited by 85 · see citing works
Self-citationRED LIGHT, AUXIN RELATIONSHIPS, AND THE PHOTOTROPIC RESPONSES OF CORN AND OAT COLEOPTILES
Briggs, W. R. (1963) · American Journal of Botany · doi:10.1002/j.1537-2197.1963.tb07195.x · Cited by 85 · see citing works
Self-citationWhippo, C. W., & Hangarter, R. P. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.102.018481 · Cited by 80 · see citing works
A Growth Regulatory Loop That Provides Homeostasis to Phytochrome A Signaling[W]
Lariguet, P., Boccalandro, H. E., Alonso, J. M., Ecker, J. R., Chory, J., Casal, J. J., & Fankhauser, C. (2003) · The Plant Cell · doi:10.1105/tpc.014563 · Cited by 74 · see citing works
Phytochrome-mediated phototropism in maize seedling shoots
Iino, M., Briggs, W. R., & Sch�fer, E. (1984) · Planta · doi:10.1007/bf00392464 · Cited by 62 · see citing works
Self-citationJanoudi, A.-K., Konjević, R., Whitelam, G. C., Gordon, W. R., & Poff, K. L. (1997) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1997.tb00997.x · Cited by 53 · see citing works
Phytochrome modulation of blue‐light‐induced phototropism
Whippo, C. W., & Hangarter, R. P. (2004) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2004.01227.x · Cited by 50 · see citing works
Characterization of Adaptation in Phototropism of Arabidopsis thaliana
Janoudi, A.-K., & Poff, K. L. (1991) · PLANT PHYSIOLOGY · doi:10.1104/pp.95.2.517 · Cited by 39 · see citing works
ACTION SPECTRUM FOR ENHANCEMENT OF PHOTOTROPISM BY Arabidopsis thaliana SEEDLINGS
Janoudi, A.-K., & Poff, K. L. (1992) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1992.tb02218.x · Cited by 37 · see citing works
Evidence for a Phytochrome-Mediated Phototropism in Etiolated Pea Seedlings
Parker, K., Baskin, T. I., & Briggs, W. R. (1989) · PLANT PHYSIOLOGY · doi:10.1104/pp.89.2.493 · Cited by 27 · see citing works
Self-citationDesensitization and Recovery of Phototropic Responsiveness in Arabidopsis thaliana
Janoudi, A.-K., & Poff, K. L. (1993) · PLANT PHYSIOLOGY · doi:10.1104/pp.101.4.1175 · Cited by 23 · see citing works
Time threshold for second positive phototropism is decreased by a preirradiation with red light.
Janoudi, A.-K., Konjević, R., Apel, P., & Poff, K. L. (1992) · PLANT PHYSIOLOGY · doi:10.1104/pp.99.4.1422 · Cited by 23 · see citing works
Flagged first, then by citations
Research works printed but not linked: 2
- Curry, G.M. (1957). Studies on the Spectral Sensitivity of Phototropism. PhD dissertation (Cambridge, MA: Harvard University).
- Scha ¨fer, E., and Nagy, F., eds (2006). Photomorphogenesis in Plants and Bacteria, 3rd ed: Function and Signal Transduction Mechanisms. (Dordrecht, The Netherlands: Springer).
Cited by
Sorted by citations
Light-Regulated Plant Growth and Development
Kami, C., Lorrain, S., Hornitschek, P., & Fankhauser, C. (2010) · Current Topics in Developmental Biology · doi:10.1016/s0070-2153(10)91002-8 · Cited by 927 · see citing works
Phytochrome Signaling Mechanisms
Li, J., Li, G., Wang, H., & Deng, X. W. (2011) · The Arabidopsis Book · doi:10.1199/tab.0148 · Cited by 566 · see citing works
Plant Flavoprotein Photoreceptors
Christie, J. M., Blackwood, L., Petersen, J., & Sullivan, S. (2015) · Plant and Cell Physiology · doi:10.1093/pcp/pcu196 · Cited by 294 · see citing works
Phototropism: Growing towards an Understanding of Plant Movement
Liscum, E., Askinosie, S. K., Leuchtman, D. L., Morrow, J., Willenburg, K. T., & Coats, D. R. (2014) · The Plant Cell · doi:10.1105/tpc.113.119727 · Cited by 215 · see citing works
Genetic improvement for root growth angle to enhance crop production
Uga, Y., Kitomi, Y., Ishikawa, S., & Yano, M. (2015) · Ikushugaku zasshi · doi:10.1270/jsbbs.65.111 · Cited by 137 · see citing works
Kaiserli, E., Sullivan, S., Jones, M. A., Feeney, K. A., & Christie, J. M. (2009) · The Plant Cell · doi:10.1105/tpc.109.067876 · Cited by 127 · see citing works
Suetsugu, N., & Wada, M. (2013) · Plant and Cell Physiology · doi:10.1093/pcp/pcs165 · Cited by 122 · see citing works
Phototropism: at the crossroads of light-signaling pathways
Goyal, A., Szarzynska, B., & Fankhauser, C. (2013) · Trends in Plant Science · doi:10.1016/j.tplants.2013.03.002 · Cited by 109 · see citing works
Molecular mechanisms and ecological function of far‐red light signalling
Sheerin, D. J., & Hiltbrunner, A. (2017) · Plant Cell & Environment · doi:10.1111/pce.12915 · Cited by 111 · see citing works
Phototropism: Some History, Some Puzzles, and a Look Ahead
Briggs, W. R. (2014) · PLANT PHYSIOLOGY · doi:10.1104/pp.113.230573 · Cited by 109 · see citing works
Self-citationAureochrome 1a Is Involved in the Photoacclimation of the Diatom Phaeodactylum tricornutum
Costa, B. S., Sachse, M., Jungandreas, A., Bártulos, C. R., Gruber, A., Jakob, T., Kroth, P. G., & Wilhelm, C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0074451 · Cited by 107 · see citing works
Phytochrome Cytoplasmic Signaling
Hughes, J. (2013) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-050312-120045 · Cited by 104 · see citing works
A phytochrome–phototropin light signaling complex at the plasma membrane
Jaedicke, K., Lichtenthäler, A. L., Meyberg, R., Zeidler, M., & Hughes, J. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1120203109 · Cited by 102 · see citing works
Light and gravity signals synergize in modulating plant development
Vandenbrink, J. P., Kiss, J. Z., Herranz, R., & Medina, F. J. (2014) · Frontiers in Plant Science · doi:10.3389/fpls.2014.00563 · Cited by 95 · see citing works
Understanding phototropism: from Darwin to today
Holland, J. J., Roberts, D., & Emmanuel Liscum, A. (2009) · Journal of Experimental Botany · doi:10.1093/jxb/erp113 · Cited by 96 · see citing works
Phytochrome Kinase Substrate 4 is phosphorylated by the phototropin 1 photoreceptor
Demarsy, E., Schepens, I., Okajima, K., Hersch, M., Bergmann, S., Christie, J., Shimazaki, K., Tokutomi, S., & Fankhauser, C. (2012) · The EMBO Journal · doi:10.1038/emboj.2012.186 · Cited by 94 · see citing works
Phototropism: Translating light into directional growth
Hohm, T., Preuten, T., & Fankhauser, C. (2012) · American Journal of Botany · doi:10.3732/ajb.1200299 · Cited by 91 · see citing works
Wu, L., McGrane, R. S., & Beattie, G. A. (2013) · mBio · doi:10.1128/mbio.00334-13 · Cited by 91 · see citing works
Tissue-Autonomous Promotion of Palisade Cell Development by Phototropin 2 inArabidopsis
Kozuka, T., Kong, S., Doi, M., Shimazaki, K., & Nagatani, A. (2011) · The Plant Cell · doi:10.1105/tpc.111.085852 · Cited by 83 · see citing works
Tsuchida-Mayama, T., Sakai, T., Hanada, A., Uehara, Y., Asami, T., & Yamaguchi, S. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04180.x · Cited by 79 · see citing works
Root phototropism: from dogma to the mechanism of blue light perception
Kutschera, U., & Briggs, W. R. (2012) · Planta · doi:10.1007/s00425-012-1597-y · Cited by 79 · see citing works
Self-citationHaga, K., & Sakai, T. (2012) · PLANT PHYSIOLOGY · doi:10.1104/pp.112.202432 · Cited by 77 · see citing works
Recent advances in understanding the molecular mechanism of chloroplast photorelocation movement
Kong, S., & Wada, M. (2013) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2013.12.004 · Cited by 73 · see citing works
Haga, K., Tsuchida-Mayama, T., Yamada, M., & Sakai, T. (2015) · The Plant Cell · doi:10.1105/tpc.15.00178 · Cited by 66 · see citing works
Moriwaki, T., Miyazawa, Y., Fujii, N., & Takahashi, H. (2012) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2012.02493.x · Cited by 71 · see citing works
Scherer, G. F. E. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/err033 · Cited by 69 · see citing works
Tseng, T.-S., & Briggs, W. R. (2010) · The Plant Cell · doi:10.1105/tpc.109.066423 · Cited by 75 · see citing works
Self-citationMolecular Genetic Analysis of Phototropism in Arabidopsis
Sakai, T., & Haga, K. (2012) · Plant and Cell Physiology · doi:10.1093/pcp/pcs111 · Cited by 66 · see citing works
Phototropism: Mechanism and Outcomes
Pedmale, U. V., Celaya, R. B., & Emmanuel Liscum, A. (2010) · The Arabidopsis Book · doi:10.1199/tab.0125 · Cited by 63 · see citing works
The Role of a 14-3-3 Protein in Stomatal Opening Mediated by PHOT2 in Arabidopsis
Tseng, T., Whippo, C. W., Hangarter, R. P., & Briggs, W. R. (2012) · The Plant Cell · doi:10.1105/tpc.111.092130 · Cited by 62 · see citing works
Self-citationNuclear Phytochrome A Signaling Promotes Phototropism in <i>Arabidopsis</i>
Kami, C., Hersch, M., Trevisan, M., Genoud, T., Hiltbrunner, A., Bergmann, S., & Fankhauser, C. (2012) · The Plant Cell · doi:10.1105/tpc.111.095083 · Cited by 55 · see citing works
Strategies of seedlings to overcome their sessile nature: auxin in mobility control
Žádníková, P., Smet, D., Zhu, Q., Straeten, D. V. D., & Benková, E. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.00218 · Cited by 53 · see citing works
Plant Phytochromes and their Phosphorylation
Hoang, Q. T. N., Han, Y., & Kim, J. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20143450 · Cited by 44 · see citing works
Cytoplasmic Phytochrome Action
Rösler, J., Jaedicke, K., & Zeidler, M. (2010) · Plant and Cell Physiology · doi:10.1093/pcp/pcq091 · Cited by 43 · see citing works
Haga, K., Hayashi, K.-I., & Sakai, T. (2014) · Plant Physiology · doi:10.1104/pp.114.244434 · Cited by 44 · see citing works
Kami, C., Allenbach, L., Zourelidou, M., Ljung, K., Schütz, F., Isono, E., Watahiki, M. K., Yamamoto, K. T., Schwechheimer, C., & Fankhauser, C. (2014) · The Plant Journal · doi:10.1111/tpj.12395 · Cited by 44 · see citing works
Preuten, T., Blackwood, L., Christie, J. M., & Fankhauser, C. (2015) · New Phytologist · doi:10.1111/nph.13299 · Cited by 38 · see citing works
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 33 · see citing works
Wang, Y., Maruhnich, S. A., Magerøy, M. H., Justice, J. R., & Folta, K. M. (2012) · Planta · doi:10.1007/s00425-012-1767-y · Cited by 33 · see citing works
Physical Control Over Endocytosis
Baluška, F., & Wan, Y. (2012) · Springer eBooks · doi:10.1007/978-3-642-32463-5_6 · Cited by 31 · see citing works
Development of transgenic crops based on photo‐biotechnology
Ganesan, M., Lee, H., Kim, J., & Song, P. (2016) · Plant Cell & Environment · doi:10.1111/pce.12887 · Cited by 31 · see citing works
Molecular insights into the phototropin control of chloroplast movements
Łabuz, J., Sztatelman, O., & Hermanowicz, P. (2022) · Journal of Experimental Botany · doi:10.1093/jxb/erac271 · Cited by 30 · see citing works
Kirchenbauer, D., Viczián, A., Ádám, É., Hegedüs, Z., Klose, C., Leppert, M., Hiltbrunner, A., Kircher, S., Schäfer, E., & Nagy, F. (2016) · New Phytologist · doi:10.1111/nph.13941 · Cited by 28 · see citing works
Investigations on the Photoregulation of Chloroplast Movement and Leaf Positioning in Arabidopsis
Han, I., Cho, H., Moni, A., Lee, A., & Briggs, W. R. (2012) · Plant and Cell Physiology · doi:10.1093/pcp/pcs098 · Cited by 28 · see citing works
Self-citationHaga, K., & Sakai, T. (2023) · Journal of Experimental Botany · doi:10.1093/jxb/erad015 · Cited by 26 · see citing works
Suetsugu, N., Kong, S., Kasahara, M., & Wada, M. (2012) · American Journal of Botany · doi:10.3732/ajb.1200308 · Cited by 25 · see citing works
Local phytochrome signalling limits root growth in light by repressing auxin biosynthesis
Spaninks, K., & Offringa, R. (2023) · Journal of Experimental Botany · doi:10.1093/jxb/erad163 · Cited by 22 · see citing works
Yamamoto, K., Suzuki, T., Aihara, Y., Haga, K., Sakai, T., & Nagatani, A. (2013) · Plant and Cell Physiology · doi:10.1093/pcp/pct184 · Cited by 22 · see citing works
The continuing arc toward phototropic enlightenment
Emmanuel Liscum, A., Nittler, P., & Koskie, K. A. (2020) · Journal of Experimental Botany · doi:10.1093/jxb/eraa005 · Cited by 21 · see citing works
Subcellular localization and turnover of Arabidopsis phototropin 1
Sullivan, S., Kaiserli, E., Tseng, T., & Christie, J. M. (2010) · Plant Signaling & Behavior · doi:10.4161/psb.5.2.11082 · Cited by 18 · see citing works
Self-citationThe action of enhancing weak light capture via phototropic growth and chloroplast movement in plants
Xin, G.-Y., Li, L.-P., Wang, P.-T., Li, X.-Y., Han, Y.-J., & Zhao, X. (2022) · Stress Biology · doi:10.1007/s44154-022-00066-x · Cited by 17 · see citing works
Blue Light-Induced Intracellular Movement of Phototropins: Functional Relevance or Red Herring?
Emmanuel Liscum, A. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.00827 · Cited by 13 · see citing works
Retzer, K., Korbei, B., & Luschnig, C. (2014) · Springer eBooks · doi:10.1007/978-3-7091-1526-8_16 · Cited by 13 · see citing works
Intricate genetic variation networks control the adventitious root growth angle in apple
Zheng, C., Shen, F., Wang, Y., Wu, T., Xu, X., Zhang, X., & Han, Z. (2020) · BMC Genomics · doi:10.1186/s12864-020-07257-8 · Cited by 12 · see citing works
New horizons in light control of plant photomorphogenesis and development
Liebers, M., & Pfannschmidt, T. (2024) · Frontiers in Photobiology · doi:10.3389/fphbi.2023.1346705 · Cited by 6 · see citing works
Phototropism in land plants: Molecules and mechanism from light perception to response
Morrow, J., Willenburg, K. T., & Emmanuel Liscum, A. (2018) · Frontiers in Biology · doi:10.1007/s11515-018-1518-y · Cited by 6 · see citing works
Plant research accelerates along the (bio)informatics superhighway
Jiménez‐Gómez, J. M., & Maloof, J. (2009) · EMBO Reports · doi:10.1038/embor.2009.116 · Cited by 5 · see citing works
Jung, Y. J., Kang, D. H., Tsevelkhoroloo, M., Moon, J. K., & Kang, K.-K. (2015) · Journal of Plant Biotechnology · doi:10.5010/jpb.2015.42.2.104 · Cited by 2 · see citing works
Sexual and asexual offspring germination in a tropical liverwort is mediated by phytochromes
Lay, C. M., Sindall, M., McLetchie, S. K., & McLetchie, D. N. (2022) · The Bryologist · doi:10.1639/0007-2745-125.2.328 · Cited by 1 · see citing works
Symposium on Plant Sensing, Response and Adaptation to the Environment
Jiménez‐Gómez, J. M., & Maloof, J. (2009)
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
Zheng, C., Shen, F., Wang, Y., Wu, T., Xu, X., Zhang, X., & Han, Z. (2020) · Figshare · doi:10.6084/m9.figshare.13317050
Zheng, C., Shen, F., Wang, Y., Wu, T., Xu, X., Zhang, X., & 韩振海 (2020) · Figshare · doi:10.6084/m9.figshare.13317023
Zheng, C., Shen, F., Wang, Y., Wu, T., Xu, X., Zhang, X., & 韩振海 (2020) · Figshare · doi:10.6084/m9.figshare.13317047
Zheng, C., Shen, F., Wang, Y., Wu, T., Xu, X., Zhang, X., & 韩振海 (2020) · Figshare · doi:10.6084/m9.figshare.13317029
Zheng, C., Shen, F., Wang, Y., Wu, T., Xu, X., Zhang, X., & 韩振海 (2020) · Figshare · doi:10.6084/m9.figshare.13317035
Zheng, C., Shen, F., Wang, Y., Wu, T., Xu, X., Zhang, X., & 韩振海 (2020) · Figshare · doi:10.6084/m9.figshare.13317041
Zheng, C., Shen, F., Wang, Y., Wu, T., Xu, X., Zhang, X., & 韩振海 (2020) · Figshare · doi:10.6084/m9.figshare.13317038
Zheng, C., Shen, F., Wang, Y., Wu, T., Xu, X., Zhang, X., & 韩振海 (2020) · Figshare · doi:10.6084/m9.figshare.13317020
Zheng, C., Shen, F., Wang, Y., Wu, T., Xu, X., Zhang, X., & 韩振海 (2020) · Figshare · doi:10.6084/m9.figshare.13317053
Zheng, C., Shen, F., Wang, Y., Wu, T., Xu, X., Zhang, X., & 韩振海 (2020) · Figshare · doi:10.6084/m9.figshare.13317032
Zheng, C., Shen, F., Wang, Y., Wu, T., Xu, X., Zhang, X., & 韩振海 (2020) · Figshare · doi:10.6084/m9.figshare.13317044
Zheng, C., Shen, F., Wang, Y., Wu, T., Xu, X., Zhang, X., & 韩振海 (2020) · Figshare · doi:10.6084/m9.figshare.13317026
Zheng, C., Shen, F., Wang, Y., Wu, T., Xu, X., Zhang, X., & 韩振海 (2020) · Figshare · doi:10.6084/m9.figshare.13317017
Su, Y. H., Tang, L. P., & Zhang, X. S. (2026) · Springer eBooks · doi:10.1007/978-981-95-7033-1_2
- Authors
- Han, I.-S., Tseng, T.-S., Eisinger, W., & Briggs, W. R.
- Affiliations
- University of Ulsan (KR)
- Carnegie Institution for Science (US)
- Santa Clara University (US)
- ORCID
- Tseng, Tong-Seung
- Venue
- The Plant Cell
- Publisher
- Oxford University Press (OUP)
- Published
- 2008-10-01
- Volume
- 20
- Issue
- 10
- Pages
- 2835-2847
- ISSN
- 1040-4651 (ISSN-L)
- 1532-298X
- PMC
- PMC2590736
- OpenAlex
- W2099538976
- Cited by
- 77
- References
- 31
- Citations by year
- 2026: 1 · 2024: 1 · 2023: 2 · 2022: 3 · 2020: 15 · 2019: 1 · 2018: 3 · 2017: 1 · 2016: 3 · 2015: 6 · 2014: 7 · 2013: 7 · 2012: 14
- FWCI
- 5.24
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model (vor)
- Locations
- The Plant Cell (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Science Foundation (0444504)
- 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
- phytochrome A, phototropin 1, subcellular localization, plasma membrane retention, phototropism, photoreversibility, far-red light, hypocotyl elongation, Arabidopsis thaliana, etiolated seedlings
- MeSH terms
- Light, Phosphoproteins, Recombinant Fusion Proteins, Protein Serine-Threonine Kinases, Arabidopsis, Protein Transport, Arabidopsis Proteins, Plants, Genetically Modified, Green Fluorescent Proteins, Phytochrome A
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review