Phototropins Promote Plant Growth in Response to Blue Light in Low Light Environments
Open accessAbstract
Phototropins (phot1 and phot2) are plant-specific blue light receptors for phototropism, chloroplast movement, leaf expansion, and stomatal opening. All these responses are thought to optimize photosynthesis by helping to capture light energy efficiently, reduce photodamage, and acquire CO2. However, experimental evidence for the promotion of plant growth through phototropins is lacking. Here, we report dramatic phototropin-dependent effects on plant growth. When plants of Arabidopsis thaliana wild type, the phot1 and phot2 mutants, and the phot1 phot2 double mutant were grown under red light, no significant growth differences were observed. However, if a very low intensity of blue light (0.1 μmol m−2 s−1) was superimposed on red light, large increases in fresh weight up to threefold were found in those plants that carried functional PHOT1 genes. When the intensity of blue light was increased to 1 μmol m−2 s−1, the growth enhancement was also found in the phot1 single mutant, but not in the double mutant, indicating that phot2 mediated similar responses as phot1 with a lower sensitivity. The effects occurred under low photosynthetically active radiation in particular. The well-known physiological phototropin-mediated responses, including chloroplast movement, stomatal opening, and leaf expansion, in the different lines tested indicated an involvement of these responses in the blue light–induced growth enhancement. We conclude that phototropins promote plant growth by controlling and integrating a variety of responses that optimize photosynthetic performance under low photosynthetically active radiation in the natural environment.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
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?
Phototropism allows plants to orient their photosynthetic organs toward the light and occurs in mosses, ferns, and angiosperms.
“Phototropism allows plants to orient their photosynthetic organs toward the light and this behavior also occurs in mosses, ferns, and angiosperms (Takemiya et al. 2005; Suetsugu and Wada, 2007b; Goyal et al. 2013; Hohm et al. 2013; Briggs, 2014).”
From The action of enhancing weak light capture via phototropic growth and chloroplast movement in plants (2022) · cites this paper as Takemiya et al. 2005
Under weak light conditions, the phot1 mutant exhibits reduced photosynthetic performance and growth by reducing chloroplast accumulation, weakening stomatal opening, and causing leaf curling.
“Under weak light conditions, phot1 mutant exhibit reduced photosynthetic performance and growth by reducing chloroplast accumulation, weakening stomatal opening, and causing leaf curling”
From The action of enhancing weak light capture via phototropic growth and chloroplast movement in plants (2022) · cites this paper as Takemiya et al., 2005
Cites
Bradford, M. M. (1976) · Analytical Biochemistry · doi:10.1016/0003-2697(76)90527-3 · Cited by 255,302 · see citing works
Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
LAEMMLI, U. K. (1970) · Nature · doi:10.1038/227680a0 · Cited by 249,961 · see citing works
Raza, H., John, A., & Nemmar, A. (2013) · Cellular Physiology and Biochemistry · doi:10.1159/000350087 · Cited by 47,311 · see citing works
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 · see citing works
Porra, R. J., Thompson, W. A., & Kriedemann, P. E. (1989) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/s0005-2728(89)80347-0 · Cited by 6,013 · see citing works
Phytochromes and light signal perception by plants—an emerging synthesis
Smith, H. (2000) · Nature · doi:10.1038/35036500 · Cited by 1,385 · see citing works
Light Signal Transduction in Higher Plants
Chen, M., Chory, J., & Fankhauser, C. (2004) · Annual Review of Genetics · doi:10.1146/annurev.genet.38.072902.092259 · Cited by 1,002 · see citing works
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 · cited 1× · see citing works
“Plasma membrane Hþ-ATPase was quantified immunologically with polyclonal antibodies as described previously (Kinoshita and Shimazaki, 1999).”
MethodSelf-citationFerns diversified in the shadow of angiosperms
Schneider, H., Schuettpelz, E., Pryer, K., Cranfill, R., Magallón, S., & Lupia, R. (2004) · Nature · doi:10.1038/nature02361 · Cited by 813 · see citing works
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 · see citing works
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 · 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
Arabidopsis 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
Kagawa, T., Sakai, T., Suetsugu, N., Oikawa, K., Ishiguro, S., Kato, T., Tabata, S., Okada, K., & Wada, M. (2001) · Science · doi:10.1126/science.291.5511.2138 · Cited by 651 · 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
Chloroplast avoidance movement reduces photodamage in plants
Kasahara, M., Kagawa, T., Oikawa, K., Suetsugu, N., Miyao, M., & Wada, M. (2002) · Nature · doi:10.1038/nature01213 · Cited by 581 · see citing works
Christie, J. M., Salomon, M., Nozue, K., Wada, M., & Briggs, W. R. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.15.8779 · Cited by 576 · 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
Salomon, M., Christie, J. M., Knieb, E., Lempert, U., & Briggs, W. R. (2000) · Biochemistry · doi:10.1021/bi000585+ · Cited by 564 · see citing works
Phototropin-related NPL1 controls chloroplast relocation induced by blue light
Jarillo, J. A., Gabrys, H., Capel, J., Alonso, J. M., Ecker, J. R., & Cashmore, A. R. (2001) · Nature · doi:10.1038/35073622 · Cited by 476 · see citing works
Kinoshita, T., & Shimazaki, K. (1999) · The EMBO Journal · doi:10.1093/emboj/18.20.5548 · Cited by 452 · see citing works
Self-citationCellular 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
Blue Light Receptors and Signal Transduction
Lin, C. (2002) · The Plant Cell · doi:10.1105/tpc.000646 · Cited by 367 · see citing works
Kasahara, M., Swartz, T. E., Olney, M. A., Onodera, A., Mochizuki, N., Fukuzawa, H., Asamizu, E., Tabata, S., Kajiya‐Kanegae, H., Takano, M., et al. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.002410 · Cited by 288 · see citing works
Phototropin LOV domains exhibit distinct roles in regulating photoreceptor function
Christie, J. M., Swartz, T. E., Bogomolni, R. A., & Briggs, W. R. (2002) · The Plant Journal · doi:10.1046/j.1365-313x.2002.01415.x · Cited by 286 · see citing works
Lin, C. (2000) · Trends in Plant Science · doi:10.1016/s1360-1385(00)01687-3 · Cited by 279 · see citing works
Folta, K. M., & Spalding, E. P. (2001) · The Plant Journal · doi:10.1046/j.1365-313x.2001.01038.x · Cited by 256 · see citing works
Responses of ferns to red light are mediated by an unconventional photoreceptor
Kawai, H., Kanegae, T., Christensen, S., Kiyosue, T., Sato, Y., Imaizumi, T., Kadota, A., & Wada, M. (2003) · Nature · doi:10.1038/nature01310 · Cited by 231 · see citing works
Ohgishi, M., Saji, K., Okada, K., & Sakai, T. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0305984101 · Cited by 215 · see citing works
A phytochrome from the fern Adiantum with features of the putative photoreceptor NPH1
Nozue, K., Kanegae, T., Imaizumi, T., Fukuda, S., Okamoto, H., Yeh, K., Lagarias, J. C., & Wada, M. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.26.15826 · Cited by 189 · see citing works
Harada, A., Sakai, T., & Okada, K. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1336802100 · Cited by 185 · see citing works
Cryptochrome blue-light photoreceptors of Arabidopsis implicated in phototropism
Ahmad, M., Jarillo, J. A., Smirnova, O., & Cashmore, A. R. (1998) · Nature · doi:10.1038/33701 · Cited by 171 · see citing works
Light and shade in the photocontrol of Arabidopsis growth
Morelli, G., & Ruberti, I. (2002) · Trends in Plant Science · doi:10.1016/s1360-1385(02)02314-2 · Cited by 167 · see citing works
The Electronic Plant Gene Register
Chen, C., Meyermans, H., Van Doorsselaere, J., Van Montagu, M., & Boerjan, W. (1998) · PLANT PHYSIOLOGY · doi:10.1104/pp.117.2.717 · Cited by 81 · see citing works
Doi, M., Shigenaga, A., Emi, T., Kinoshita, T., & Shimazaki, K. (2004) · Journal of Experimental Botany · doi:10.1093/jxb/erh044 · Cited by 76 · see citing works
Self-citationGalen, C., Huddle, J. A., & Emmanuel Liscum, A. (2004) · Evolution · doi:10.1111/j.0014-3820.2004.tb01675.x · Cited by 58 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Phototropin Blue-Light Receptors
Christie, J. M. (2007) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.58.032806.103951 · Cited by 937 · see citing works
Light Regulation of Stomatal Movement
Shimazaki, K., Doi, M., Assmann, S. M., & Kinoshita, T. (2007) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.57.032905.105434 · Cited by 924 · see citing works
Self-citationLight-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
Franklin, K. A. (2008) · New Phytologist · doi:10.1111/j.1469-8137.2008.02507.x · Cited by 801 · see citing works
Huché‐Thélier, L., Crespel, L., Gourrierec, J. L., Morel, P., Sakr, S., & Leduc, N. (2015) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2015.06.009 · Cited by 462 · see citing works
Johkan, M., Shoji, K., Goto, F., Hahida, S., & Yoshihara, T. (2011) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2011.08.010 · Cited by 378 · see citing works
Optogenetic manipulation of stomatal kinetics improves carbon assimilation, water use, and growth
Papanatsiou, M., Petersen, J., Henderson, L., Wang, Y., Christie, J. M., & Blatt, M. R. (2019) · Science · doi:10.1126/science.aaw0046 · Cited by 311 · see citing works
Landi, M., Živčák, M., Sytar, O., Brestič, M., & Allakhverdiev, S. I. (2019) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2019.148131 · Cited by 301 · 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
Blue light-induced autophosphorylation of phototropin is a primary step for signaling
Inoue, S.-I., Kinoshita, T., Matsumoto, M., Nakayama, K. I., Doi, M., & Shimazaki, K.-I. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0709189105 · Cited by 269 · see citing works
Self-citationVandenbussche, F., Pierik, R., Millenaar, F. F., Voesenek, L. A. C. J., & Straeten, D. V. D. (2005) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2005.07.007 · Cited by 259 · see citing works
Keller, M. M., Jaillais, Y., Pedmale, U. V., Moreno, J. E., Chory, J., & Ballaré, C. L. (2011) · The Plant Journal · doi:10.1111/j.1365-313x.2011.04598.x · Cited by 259 · see citing works
Contributions of green light to plant growth and development
Wang, Y., & Folta, K. M. (2013) · American Journal of Botany · doi:10.3732/ajb.1200354 · Cited by 249 · see citing works
Blue Light Induces a Distinct Starch Degradation Pathway in Guard Cells for Stomatal Opening
Horrer, D., Flütsch, S., Pazmiño, D. M., Matthews, J. S. A., Thalmann, M., Nigro, A., Leonhardt, N., Lawson, T., & Santelia, D. (2016) · Current Biology · doi:10.1016/j.cub.2015.12.036 · Cited by 227 · 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
LOV Domain-Containing F-Box Proteins: Light-Dependent Protein Degradation Modules in Arabidopsis
Ito, S., Song, Y. H., & Imaizumi, T. (2012) · Molecular Plant · doi:10.1093/mp/sss013 · Cited by 211 · see citing works
Zheng, L., & Labeke, M. V. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.00917 · Cited by 201 · see citing works
Regulation of Transpiration to Improve Crop Water Use
Yoo, C. Y., Pence, H. E., Hasegawa, P. M., & Mickelbart, M. V. (2009) · Critical Reviews in Plant Sciences · doi:10.1080/07352680903173175 · Cited by 190 · see citing works
PHYTOCHROME 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
Oikawa, K., Yamasato, A., Kong, S.-G., Kasahara, M., Nakai, M., Takahashi, F., Ogura, Y., Kagawa, T., & Wada, M. (2008) · Plant Physiology · doi:10.1104/pp.108.123075 · Cited by 181 · see citing works
Effects of Light on Secondary Metabolites in Selected Leafy Greens: A Review
Thoma, F., Somborn, A., Schlehuber, D., Keuter, V., & Deerberg, G. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.00497 · Cited by 189 · see citing works
Timm, S., Wittmiß, M., Gamlien, S., Ewald, R., Florian, A., Frank, M., Wirtz, M., Hell, R., Fernie, A. R., & Bauwe, H. (2015) · The Plant Cell · doi:10.1105/tpc.15.00105 · Cited by 171 · see citing works
de Carbonnel, M., Davis, P., Roelfsema, M. R. G., Inoue, S.-I., Schepens, I., Lariguet, P., Geisler, M., Shimazaki, K.-I., Hangarter, R., & Fankhauser, C. (2010) · Plant Physiology · doi:10.1104/pp.109.150441 · Cited by 161 · see citing works
Self-citationLeaf Positioning of Arabidopsis in Response to Blue Light
Inoue, S.-I., Kinoshita, T., Takemiya, A., Doi, M., & Shimazaki, K.-I. (2008) · Molecular Plant · doi:10.1093/mp/ssm001 · Cited by 156 · see citing works
Self-citationWillige, B. C., Ahlers, S., Zourelidou, M., Barbosa, I. C. R., Demarsy, E., Trevisan, M., Davis, P. A., Roelfsema, M. R. G., Hangarter, R., Fankhauser, C., et al. (2013) · The Plant Cell · doi:10.1105/tpc.113.111484 · Cited by 149 · see citing works
Physical interaction between peroxisomes and chloroplasts elucidated by in situ laser analysis
Oikawa, K., Matsunaga, S., Mano, S., Kondo, M., Yamada, K., Hayashi, M., Kagawa, T., Kadota, A., Sakamoto, W., Higashi, S., et al. (2015) · Nature Plants · doi:10.1038/nplants.2015.35 · Cited by 144 · see citing works
Proteomic analysis of the response to high-salinity stress in Physcomitrella patens
Wang, X., Yang, P., Gao, Q., Liu, X., Kuang, T., Shen, S., & He, Y. (2008) · Planta · doi:10.1007/s00425-008-0727-z · Cited by 142 · see citing works
Protein phosphatase 1 positively regulates stomatal opening in response to blue light in Vicia faba
Takemiya, A., Kinoshita, T., Asanuma, M., & Shimazaki, K. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0602503103 · Cited by 139 · see citing works
Self-citationLOV to BLUF: Flavoprotein Contributions to the Optogenetic Toolkit
Christie, J. M., Gawthorne, J. A., Young, G., Fraser, N. J., & Roe, A. J. (2012) · Molecular Plant · doi:10.1093/mp/sss020 · Cited by 135 · see citing works
Photoreceptors and Control of Horticultural Plant Traits
Folta, K. M., & Carvalho, S. D. (2015) · HortScience · doi:10.21273/hortsci.50.9.1274 · Cited by 134 · 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
Chloroplast Accumulation Response Enhances Leaf Photosynthesis and Plant Biomass Production
Gotoh, E., Suetsugu, N., Yamori, W., Ishishita, K., Kiyabu, R., Fukuda, M., Higa, T., Shirouchi, B., & Wada, M. (2018) · Plant Physiology · doi:10.1104/pp.18.00484 · Cited by 128 · see citing works
Effects of light sources on major flavonoids and antioxidant activity in common buckwheat sprouts
Nam, T. G., Kim, D., & Eom, S. H. (2017) · Food Science and Biotechnology · doi:10.1007/s10068-017-0204-1 · Cited by 124 · see citing works
Mawphlang, O. I. L., & Kharshiing, E. V. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.01181 · Cited by 123 · see citing works
Chloroplast photorelocation movement mediated by phototropin family proteins in green plants
Suetsugu, N., & Wada, M. (2007) · bchm · doi:10.1515/bc.2007.118 · Cited by 123 · see citing works
Wollaeger, H., & Runkle, E. S. (2014) · HortScience · doi:10.21273/hortsci.49.6.734 · Cited by 113 · see citing works
Boccalandro, H. E., Giordano, C. V., Ploschuk, E. L., Píccoli, P., Bottini, R., & Casal, J. J. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.187237 · Cited by 110 · 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
In Vivo Phosphorylation Site Mapping and Functional Characterization of Arabidopsis Phototropin 1
Sullivan, S., Thomson, C. E., Lamont, D. J., Jones, M. A., & Christie, J. M. (2008) · Molecular Plant · doi:10.1093/mp/ssm017 · Cited by 107 · see citing works
Blue light signalling in chloroplast movements
Banas, A. K., Aggarwal, C., Labuz, J., Sztatelman, O., & Gabrys, H. (2012) · Journal of Experimental Botany · doi:10.1093/jxb/err429 · Cited by 105 · 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
Baidya, A., Akter, T., Islam, M. R., Shah, A. K. M. A., Hossaın, M. A., Salam, M. A., & Paul, S. I. (2021) · Heliyon · doi:10.1016/j.heliyon.2021.e08525 · Cited by 93 · see citing works
Interaction specificity of Arabidopsis 14‐3‐3 proteins with phototropin receptor kinases
Sullivan, S., Thomson, C. E., Kaiserli, E., & Christie, J. M. (2009) · FEBS Letters · doi:10.1016/j.febslet.2009.06.011 · Cited by 85 · see citing works
Jones, M. A., Feeney, K. A., Kelly, S. M., & Christie, J. M. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m605969200 · Cited by 86 · see citing works
Wagner, R., Dietzel, L., Bräutigam, K., Fischer, W., & Pfannschmidt, T. (2008) · Planta · doi:10.1007/s00425-008-0760-y · Cited by 85 · see citing works
Phototropin signaling and stomatal opening as a model case
Inoue, S., Takemiya, A., & Shimazaki, K. (2010) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2010.09.002 · Cited by 83 · see citing works
Self-citationExploring the Potential use of Photo-Selective Nets for Fruit Growth Regulation in Apple
Bastías, R. M., Manfrini, L., & Grappadelli, L. C. (2012) · Chilean journal of agricultural research · doi:10.4067/s0718-58392012000200010 · Cited by 85 · 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
Self-citationEffects of light pollution on tree phenology in the urban environment
Škvareninová, J., Tuhárska, M., Škvarenina, J., Babálová, D., Slobodníková, L., Slobodník, B., Středová, H., & Minďáš, J. (2017) · Moravian Geographical Reports · doi:10.1515/mgr-2017-0024 · Cited by 82 · see citing works
Molecular structure and regulation of phototropin kinase by blue light
Tokutomi, S., Matsuoka, D., & Zikihara, K. (2007) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2007.09.010 · Cited by 81 · see citing works
Functional Analyses of the Activation Loop of Phototropin2 in Arabidopsis
Inoue, S.-I., Matsushita, T., Tomokiyo, Y., Matsumoto, M., Nakayama, K. I., Kinoshita, T., & Shimazaki, K. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.175943 · Cited by 79 · see citing works
Self-citationF-Box Protein FBX92 Affects Leaf Size in Arabidopsis thaliana
Baute, J., Polyn, S., Block, J. D., Blomme, J., Lijsebettens, M. V., & Inz�, D. (2017) · Plant and Cell Physiology · doi:10.1093/pcp/pcx035 · Cited by 77 · see citing works
Doi, M., & Shimazaki, K. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.118950 · Cited by 76 · see citing works
Self-citationPhototropins and Blue Light-dependent Calcium Signaling in Higher Plants†
Harada, A., & Shimazaki, K. (2007) · Photochemistry and Photobiology · doi:10.1562/2006-03-08-ir-837 · Cited by 73 · see citing works
Self-citationTrippens, J., Greiner, A., Schellwat, J., Neukam, M., Rottmann, T., Lu, Y., Kateriya, S., Hegemann, P., & Kreimer, G. (2012) · The Plant Cell · doi:10.1105/tpc.112.103523 · Cited by 75 · see citing works
Blue Light-Dependent Nuclear Positioning in Arabidopsis thaliana Leaf Cells
Iwabuchi, K., Sakai, T., & Takagi, S. (2007) · Plant and Cell Physiology · doi:10.1093/pcp/pcm095 · Cited by 75 · see citing works
Kong, S.-G., Arai, Y., Suetsugu, N., Yanagida, T., & Wada, M. (2013) · The Plant Cell · doi:10.1105/tpc.113.109694 · Cited by 71 · see citing works
Sullivan, S., Waksman, T., Paliogianni, D., Henderson, L., Lütkemeyer, M., Suetsugu, N., & Christie, J. M. (2021) · Nature Communications · doi:10.1038/s41467-021-26333-5 · Cited by 74 · see citing works
Responses of supplemental blue light on flowering and stem extension growth of cut chrysanthemum
Jeong, S. W., Hogewoning, S. W., & van Ieperen, W. (2013) · Scientia Horticulturae · doi:10.1016/j.scienta.2013.11.006 · Cited by 72 · see citing works
Takemiya, A., Yamauchi, S., Yano, T., Ariyoshi, C., & Shimazaki, K. (2012) · Plant and Cell Physiology · doi:10.1093/pcp/pcs073 · Cited by 72 · see citing works
Self-citationNazir, M., Ullah, M. A., Younas, M. U., Siddiquah, A., Shah, M., Giglioli‐Guivarc’h, N., Hano, C., & Abbasi, B. H. (2020) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-020-01844-z · Cited by 68 · see citing works
Ambient Temperature-Responsive Mechanisms Coordinate Regulation of Flowering Time
Susila, H., Nasim, Z., & Ahn, J. H. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19103196 · Cited by 65 · 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
Davey, M. W., Graham, N. S., Vanholme, B., Swennen, R. L., May, S. T., & Keulemans, J. (2009) · BMC Genomics · doi:10.1186/1471-2164-10-436 · Cited by 61 · see citing works
Silva, T. D., Batista, D. S., Fortini, E. A., de Castro, K. M., Felipe, S. H. S., Fernandes, A. M., Sousa, R. M. D. J., Chagas, K., da Silva, J. V. S., Correia, L. N. F., et al. (2019) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2019.111761 · Cited by 62 · see citing works
Photoprotective function of chloroplast avoidance movement: In vivo chlorophyll fluorescence study
Sztatelman, O., Waloszek, A., Katarzyna Banaś, A., & Gabryś, H. (2010) · Journal of Plant Physiology · doi:10.1016/j.jplph.2009.12.015 · Cited by 59 · see citing works
New Insights into the Regulation of Stomatal Opening by Blue Light and Plasma Membrane H+-ATPase
Kinoshita, T., & Hayashi, Y. (2011) · International review of cytology · doi:10.1016/b978-0-12-386039-2.00003-1 · Cited by 58 · see citing works
Self-citationO’Carrigan, A., Babla, M. H., Wang, F., Liu, X., Mak, M., Thomas, R. G., Bellotti, B., & Chen, Z. (2014) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2014.05.012 · Cited by 56 · see citing works
Kong, Y., & Zheng, Y. (2019) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2019.103967 · Cited by 54 · see citing works
Shades of green: untying the knots of green photoperception
Battle, M. W., Vegliani, F., & Jones, M. A. (2020) · Journal of Experimental Botany · doi:10.1093/jxb/eraa312 · Cited by 53 · see citing works
Zeitlupe Senses Blue-Light Fluence To Mediate Circadian Timing in Arabidopsis thaliana
Pudasaini, A., & Zoltowski, B. D. (2013) · Biochemistry · doi:10.1021/bi401027n · Cited by 53 · see citing works
Possible Involvement of Phototropins in Leaf Movement of Kidney Bean in Response to Blue Light
Inoue, S.-I., Kinoshita, T., & Shimazaki, K.-I. (2005) · Plant Physiology · doi:10.1104/pp.105.062026 · Cited by 52 · see citing works
Self-citationPERK–KIPK–KCBP signalling negatively regulates root growth in Arabidopsis thaliana
Humphrey, T., Haasen, K. E., Aldea-Brydges, M. G., Sun, H., Zayed, Y., Indriolo, E., & Goring, D. R. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/eru390 · Cited by 52 · see citing works
Molecular basis of chloroplast photorelocation movement
Kong, S.-G., & Wada, M. (2016) · Journal of Plant Research · doi:10.1007/s10265-016-0788-1 · Cited by 50 · see citing works
Pocock, T. H. (2015) · HortScience · doi:10.21273/hortsci.50.9.1281 · Cited by 50 · see citing works
Sa, N., Rawat, R., Thornburg, C. K., Walker, K. D., & Roje, S. (2016) · The Plant Journal · doi:10.1111/tpj.13291 · Cited by 48 · see citing works
Defining the Site of Light Perception and Initiation of Phototropism in Arabidopsis
Preuten, T., Hohm, T., Bergmann, S., & Fankhauser, C. (2013) · Current Biology · doi:10.1016/j.cub.2013.07.079 · Cited by 46 · see citing works
Pislariu, C. I., & Dickstein, R. (2007) · PLANT PHYSIOLOGY · doi:10.1104/pp.106.092494 · Cited by 46 · see citing works
Hart, J. E., Sullivan, S., Hermanowicz, P., Petersen, J., Díaz-Ramos, L. A., Hoey, D. J., Łabuz, J., & Christie, J. M. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1902915116 · Cited by 46 · see citing works
An, J., Wei, X., & Huo, H. (2022) · BMC Plant Biology · doi:10.1186/s12870-022-03657-y · Cited by 44 · see citing works
Chloroplast and nuclear photorelocation movements
Wada, M. (2016) · Proceedings of the Japan Academy Series B · doi:10.2183/pjab.92.387 · Cited by 44 · see citing works
Wang, P., Li, Z., Li, H., Zhang, D., Wang, W., Xu, X., Xie, Q., Duan, Z., Xia, X., Guo, G., et al. (2023) · New Crops · doi:10.1016/j.ncrops.2023.12.002 · Cited by 44 · see citing works
Kumar, R., Sharma, S., & Pathania, V. (2013) · Journal of Essential Oil Research · doi:10.1080/10412905.2012.742467 · Cited by 43 · see citing works
Perera, W. P. T. D., Navaratne, S. B., & Wickramasinghe, I. (2022) · Postharvest Biology and Technology · doi:10.1016/j.postharvbio.2022.111955 · Cited by 43 · see citing works
Optimal Hyperspectral Characteristics Determination for Winter Wheat Yield Prediction
Zhang, Y., Qin, Q., Ren, H., Sun, Y., Li, M., Zhang, T., & Ren, S. (2018) · Remote Sensing · doi:10.3390/rs10122015 · Cited by 43 · see citing works
Harada, A., Takemiya, A., Inoue, S., Sakai, T., & Shimazaki, K. (2012) · Plant and Cell Physiology · doi:10.1093/pcp/pcs094 · Cited by 41 · see citing works
Self-citationSPA proteins: SPAnning the gap between visible light and gene expression
Menon, C., Sheerin, D. J., & Hiltbrunner, A. (2016) · Planta · doi:10.1007/s00425-016-2509-3 · Cited by 40 · see citing works
Genetical Genomics Reveals Large Scale Genotype-By-Environment Interactions in Arabidopsis thaliana
Snoek, B. L., Terpstra, I. R., Dekter, R. W., den Ackerveken, G. F. J. M. V., & Peeters, A. J. M. (2013) · Frontiers in Genetics · doi:10.3389/fgene.2012.00317 · Cited by 40 · see citing works
Takemiya, A., & Shimazaki, K. (2016) · Journal of Plant Research · doi:10.1007/s10265-015-0780-1 · Cited by 40 · see citing works
Self-citationKusuma, P., Swan, B., & Bugbee, B. G. (2021) · Plants · doi:10.3390/plants10040637 · Cited by 39 · 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
Arcel, M. M., Lin, X., Huang, J., Wu, J., & Zheng, S. (2021) · Journal of Physics Conference Series · doi:10.1088/1742-6596/1732/1/012178 · Cited by 38 · see citing works
López‐Juez, E., Bowyer, J. R., & Sakai, T. (2007) · Planta · doi:10.1007/s00425-007-0599-7 · Cited by 37 · see citing works
Halavaty, A. S., & Moffat, K. (2013) · Acta Crystallographica Section F Structural Biology and Crystallization Communications · doi:10.1107/s1744309113029199 · Cited by 36 · see citing works
Phototropin-mediated perception of light direction in leaves regulates blade flattening
Legris, M., Szarzyńska, B., Trévisan, M., Petrolati, L. A., & Fankhauser, C. (2021) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiab410 · Cited by 31 · see citing works
Primary Processes During the Light‐signal Transduction of Phototropin
Matsuoka, D., Iwata, T., Zikihara, K., Kandori, H., & Tokutomi, S. (2006) · Photochemistry and Photobiology · doi:10.1562/2006-03-29-ra-861 · Cited by 34 · 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
Self-citationWang, 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
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 · see citing works
CIPK23 regulates blue light‐dependent stomatal opening in Arabidopsis thaliana
Inoue, S., Kaiserli, E., Zhao, X., Waksman, T., Takemiya, A., Okumura, M., Takahashi, H., Seki, M., Shinozaki, K., Endo, Y., et al. (2020) · The Plant Journal · doi:10.1111/tpj.14955 · Cited by 33 · see citing works
Self-citation
- Authors
- Takemiya, A., Inoue, S.-I., Doi, M., Kinoshita, T., & Shimazaki, K.-I.
- Affiliations
- Kyushu University (JP)
- Venue
- The Plant Cell
- Publisher
- Oxford University Press (OUP)
- Published
- 2005-04-01
- Volume
- 17
- Issue
- 4
- Pages
- 1120-1127
- ISSN
- 1040-4651 (ISSN-L)
- 1532-298X
- OpenAlex
- W2130280374
- Cited by
- 279
- References
- 36
- Citations by year
- 2026: 13 · 2025: 13 · 2024: 13 · 2023: 16 · 2022: 15 · 2021: 21 · 2020: 15 · 2019: 15 · 2018: 17 · 2017: 15 · 2016: 12 · 2015: 10 · 2014: 10 · 2013: 16 · 2012: 14
- FWCI
- 13.99
- Type
- journal article
- Language
- en
- Open access
- green
- dx.doi.org
- Licence
- academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model (vor)
- Locations
- The Plant Cell (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (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 › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Photosynthetic Processes and Mechanisms
- Keywords
- phototropin, phot1, phot2, blue light, low-light conditions, plant growth, photosynthetically active radiation, phototropism, chloroplast movement, stomatal opening, leaf expansion, Arabidopsis thaliana, photomorphogenesis
- MeSH terms
- Acclimatization, Light, Mutation, Phosphoproteins, Photosynthesis, Protein Serine-Threonine Kinases, Arabidopsis, Gene Expression Regulation, Plant, Plant Leaves, Arabidopsis Proteins
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