Cellular and Subcellular Localization of Phototropin 1
Open accessAbstract
Phototropin 1 (phot1) is a Ser/Thr photoreceptor kinase that binds two molecules of flavin mononucleotide as its chromophores and undergoes autophosphorylation in response to blue light. Phot1 is plasma membrane associated and, as with phot2, has been shown to function as a photoreceptor for phototropism, blue light-induced chloroplast movement, and blue light-induced stomatal opening. Phot1 likely also plays a redundant role with phot2 in regulating the rate of leaf expansion. Understanding the mechanism(s) by which phot1 initiates these four different responses requires, at minimum, knowledge of where the photoreceptor is located. Therefore, we transformed a phot1 null mutant of Arabidopsis with a construct encoding translationally fused phot1-green fluorescent protein (GFP) under the control of the endogenous PHOT1 promoter and investigated its cellular and subcellular distribution. This PHOT1-GFP construct complements the mutant phenotype, restoring second positive curvature. Phot1 is expressed strongly in dividing and elongating cortical cells in the apical hook and in the root elongation zone in etiolated seedlings. It is localized evenly to the plasma membrane region in epidermal cells but is confined largely to the plasma membrane region of the transverse cell walls in the cortical cells of both root and hypocotyl. It is found at both apical and basal ends of these cortical cells. In light-grown plants, phot1-GFP is localized largely in the plasma membrane regions adjacent to apical and basal cell end walls in the elongating inflorescence stem, where the photoreceptor is expressed strongly in the vascular parenchyma and leaf vein parenchyma. Phot1 also is localized to the plasma membrane region of leaf epidermal cells, mesophyll cells, and guard cells, where its distribution is uniform. Although phot1 is localized consistently to the plasma membrane region in etiolated seedlings, a fraction becomes released to the cytoplasm in response to blue light. Possible relationships between observed phot1 distribution and the various physiological responses activated by blue light are discussed.
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?
Although phot1 and phot2 do not possess a transmembrane domain, they localize to the inner side of the cytoplasmic membrane in the dark.
“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 Sakamoto and Briggs, 2002
The Introduction (page not provided) says phot1 has no obvious membrane-spanning domain and is associated with the inner surface of the plasma membrane in etiolated seedlings. It says only that phot2 activity is associated with a membrane fraction; phot2 localization to the plasma membrane is described as likely, not established. The claim therefore overstates what this paper supports about phot2. (LLM, conf=0.88)
Experimental — accuracy not yet measuredUnder blue light irradiation, part of PHOT1 detaches from the cell membrane and disperses in the cytoplasm, whereas some PHOT2 proteins can be coupled to the Golgi apparatus.
“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 Sakamoto and Briggs, 2002
The paper’s opening summary and discussion (page numbers not supplied) report that a fraction of phot1 moves from the plasma-membrane region into the cytoplasm in response to blue light. They do not support the sentence’s phot2–Golgi claim; the paper says comparable studies of phot2 localization were still in progress. (LLM, conf=0.90)
Experimental — accuracy not yet measured
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
A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures
Murashige, T., & Skoog, F. K. (1962) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1962.tb08052.x · Cited by 67,420 · see citing works
PAS Domains: Internal Sensors of Oxygen, Redox Potential, and Light
Taylor, B. L., & Zhulin, I. B. (1999) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.63.2.479-506.1999 · Cited by 1,632 · see citing works
Regulation of Polar Auxin Transport by AtPIN1 in <i>Arabidopsis</i> Vascular Tissue
Gälweiler, L., Guan, C., Müller, A., Wisman, E., Mendgen, K., Yephremov, A., & Palme, K. (1998) · Science · doi:10.1126/science.282.5397.2226 · Cited by 1,530 · see citing works
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 · see citing works
G UARD C ELL S IGNAL T RANSDUCTION
Schroeder, J. I., Allen, G. J., Hugouvieux, V., Kwak, J. M., & Waner, D. (2001) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.52.1.627 · Cited by 1,154 · see citing works
Arabidopsis AUX1 Gene: A Permease-Like Regulator of Root Gravitropism
Bennett, M. J., Marchant, A., Green, H. G., May, S. T., Ward, S. P., Millner, P. A., Walker, A. R., Schulz, B., & Feldmann, K. A. (1996) · Science · doi:10.1126/science.273.5277.948 · Cited by 1,043 · see citing works
Cutler, S. R., Ehrhardt, D. W., Griffitts, J. S., & Somerville, C. R. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.7.3718 · Cited by 988 · see citing works
AtPIN2 defines a locus of Arabidopsis for root gravitropism control
Müller, A., Guan, C., Gälweiler, L., Tänzler, P., Huijser, P., Marchant, A., Parry, G., Bennett, M. J., Wisman, E., & Palme, K. J. (1998) · The EMBO Journal · doi:10.1093/emboj/17.23.6903 · Cited by 900 · 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 2× · see citing works
“The strongest signals detected in the leaf epidermis arose from the guard cells (Figures 4A and 4C), which is not surprising given the recent evidence that phot1 serves as one of the photoreceptors for blue light–activated stomatal opening (Kinoshita et al., 2002).”
BackgroundPhototropins 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
Self-citationCoordinated Polar Localization of Auxin Efflux Carrier PIN1 by GNOM ARF GEF
Steinmann, T., Geldner, N., Grebe, M., Mangold, S., Jackson, C. L., Paris, S., Gälweiler, L., Palme, K. J., & Jürgens, G. (1999) · Science · doi:10.1126/science.286.5438.316 · Cited by 761 · 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-citationKagawa, 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
Swarup, R., Friml, J., Marchant, A., Ljung, K., Sandberg, G., Palme, K. J., & Bennett, M. J. (2001) · Genes & Development · doi:10.1101/gad.210501 · Cited by 645 · 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-citationChristie, 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
Self-citationSalomon, M., Christie, J. M., Knieb, E., Lempert, U., & Briggs, W. R. (2000) · Biochemistry · doi:10.1021/bi000585+ · Cited by 564 · see citing works
Self-citationPhototropin-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
Blue-Light Photoreceptors in Higher Plants
Briggs, W. R., & Huala, E. (1999) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.15.1.33 · Cited by 395 · see citing works
Self-citationBlue light activates electrogenic ion pumping in guard cell protoplasts of Vicia faba
Assmann, S. M., Simoncini, L., & Schroeder, J. I. (1985) · Nature · doi:10.1038/318285a0 · Cited by 393 · see citing works
Photoexcited Structure of a Plant Photoreceptor Domain Reveals a Light-Driven Molecular Switch
Crosson, S., & Moffat, K. (2002) · The Plant Cell · doi:10.1105/tpc.010475 · Cited by 350 · 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
Self-citationFolta, K. M., & Spalding, E. P. (2001) · The Plant Journal · doi:10.1046/j.1365-313x.2001.01038.x · Cited by 256 · see citing works
Leaf expansion – an integrating plant behaviour
Volkenburgh, E. V. (1999) · Plant Cell & Environment · doi:10.1046/j.1365-3040.1999.00514.x · Cited by 225 · see citing works
An optomechanical transducer in the blue light receptor phototropin from Avena sativa
Salomon, M., Eisenreich, W., Dürr, H., Schleicher, E., Knieb, E., Massey, V., Rüdiger, W., Müller, F., Bacher, A., & Richter, G. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.221455298 · Cited by 212 · see citing works
Baum, G., Long, J. C., Jenkins, G. I., & TREWAVAS, A. J. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.23.13554 · Cited by 211 · see citing works
Blue Light Sensing in Higher Plants
Christie, J. M., & Briggs, W. R. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.r100004200 · Cited by 189 · see citing works
Self-citationLight and Stomatal Function: Blue Light Stimulates Swelling of Guard Cell Protoplasts
Zeiger, E., & Hepler, P. K. (1977) · Science · doi:10.1126/science.196.4292.887 · Cited by 150 · see citing works
Sato, Y., Wada, M., & Kadota, A. (2001) · Journal of Cell Science · doi:10.1242/jcs.114.2.269 · Cited by 148 · see citing works
Hwang, J., Suh, S., Yi, H., Kim, J., & Lee, Y. (1997) · PLANT PHYSIOLOGY · doi:10.1104/pp.115.2.335 · Cited by 144 · see citing works
Gallagher, S. P., Short, T. W., Ray, P. M., Pratt, L. H., & Briggs, W. R. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.21.8003 · Cited by 129 · see citing works
Self-citationSGR1, SGR2, and SGR3: Novel Genetic Loci Involved in Shoot Gravitropism in Arabidopsis thaliana
Fukaki, H., Fujisawa, H., & Tasaka, M. (1996) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.3.945 · Cited by 127 · see citing works
Kagawa, T., & Wada, M. (2000) · Plant and Cell Physiology · doi:10.1093/pcp/41.1.84 · Cited by 123 · see citing works
Arabidopsis Contains at Least Four Independent Blue-Light-Activated Signal Transduction Pathways1
Lascève, G., Leymarie, J., Olney, M. A., Emmanuel Liscum, A., Christie, J. M., Vavasseur, A., & Briggs, W. R. (1999) · PLANT PHYSIOLOGY · doi:10.1104/pp.120.2.605 · Cited by 121 · see citing works
Self-citationBriggs, W. R. (1964) · Photophysiology · doi:10.1016/b978-1-4832-2798-6.50015-8 · Cited by 102 · see citing works
Self-citationShort, T. W., & Briggs, W. R. (1990) · PLANT PHYSIOLOGY · doi:10.1104/pp.92.1.179 · Cited by 101 · see citing works
Self-citationPhototropins: A New Family of Flavin-Binding Blue Light Receptors in Plants
Briggs, W. R., Christie, J. M., & Salomon, M. (2001) · Antioxidants and Redox Signaling · doi:10.1089/15230860152664975 · Cited by 92 · see citing works
Self-citationBlue- and red-light action in photoorientation of chloroplasts in Adiantum protonemata
Yatsuhashi, H., Kadota, A., & Wada, M. (1985) · Planta · doi:10.1007/bf00392210 · Cited by 89 · see citing works
Kagawa, T., & Wada, M. (1996) · Planta · doi:10.1007/bf00620067 · Cited by 79 · see citing works
Influence of calcium on blue-light-induced chloroplast movement in Lemna trisulca L.
Tlalka, M., & Gabryś, H. (1993) · Planta · doi:10.1007/bf00198211 · Cited by 70 · see citing works
Expression Patterns and Promoter Activity of the Cold-Regulated Gene ci21A of Potato
Schneider, A., Salamini, F., & Gebhardt, C. (1997) · PLANT PHYSIOLOGY · doi:10.1104/pp.113.2.335 · Cited by 67 · see citing works
Blue Light-Induced Phosphorylation of a Plasma Membrane-Associated Protein in Zea mays L
Palmer, J. M., Short, T. W., Gallagher, S. R., & Briggs, W. R. (1993) · PLANT PHYSIOLOGY · doi:10.1104/pp.102.4.1211 · Cited by 60 · see citing works
Self-citationKadota, A., & Wada, M. (1992) · Journal of Plant Research · doi:10.1007/bf02489420 · Cited by 60 · see citing works
DIAPHOTOTROPIC MOVEMENT OF THE LEAVES OF MALVA NEGLECTA
Yin, H. C. (1938) · American Journal of Botany · doi:10.1002/j.1537-2197.1938.tb09178.x · Cited by 58 · see citing works
Untersuchungen über die Phototaxis der Chloroplasten
Voerkel, S. H. (1933) · Planta · doi:10.1007/bf01909872 · Cited by 54 · see citing works
Short, T. W., Reymond, P., & Briggs, W. R. (1993) · PLANT PHYSIOLOGY · doi:10.1104/pp.101.2.647 · Cited by 51 · see citing works
Self-citationLight-stimulated cell expansion in bean (Phaseolus vulgaris L.) leaves
Volkenburgh, E. V., & Cleland, R. E. (1990) · Planta · doi:10.1007/bf00239986 · Cited by 42 · see citing works
Intracellular trafficking of photoreceptors during light-induced signal transduction in plants
Nagy, F., Kircher, S., & Schäfer, E. (2001) · Journal of Cell Science · doi:10.1242/jcs.114.3.475 · Cited by 42 · see citing works
Hager, A., & Brich, M. (1993) · Planta · doi:10.1007/bf00198221 · Cited by 41 · see citing works
Koller, D. (2000) · Advances in botanical research · doi:10.1016/s0065-2296(00)33041-5 · Cited by 34 · see citing works
Light-Stimulated Cotyledon Expansion in the blu3 and hy4 Mutants of Arabidopsis thaliana
Blum, D. E., Neff, M. M., & Volkenburgh, E. V. (1994) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.4.1433 · Cited by 34 · see citing works
Light-stimulated cell expansion in bean (Phaseolus vulgaris L.) leaves
Volkenburgh, E. V., Cleland, R. E., & Watanabe, M. (1990) · Planta · doi:10.1007/bf00239987 · Cited by 33 · see citing works
1 Development of the Leaf Epidermis
Becraft, P. W. (1999) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(08)60313-0 · Cited by 30 · see citing works
Salomon, M., Zacherl, M., & R�diger, W. (1996) · Planta · doi:10.1007/bf00195724 · Cited by 22 · see citing works
Rapid blue-light-induced phosphorylation of plasma-membrane-associated proteins in wheat
Sharma, V. K., Jain, P. K., Maheshwari, S. C., & Khurana, J. P. (1997) · Phytochemistry · doi:10.1016/s0031-9422(96)00624-3 · Cited by 18 · see citing works
Koller, D., Ritter, S., Briggs, W. R., & Schäfer, E. (1990) · Planta · doi:10.1007/bf02411536 · Cited by 18 · see citing works
Self-citation
Flagged first, then by citations
Research works printed but not linked: 4
- Briggs, W.R., and Christie, J.M. (2002). Phototropin 1 and phototropin2: Two versatile plant blue-light receptors. Trends Plant Sci. 7, 204–210. [DOI] [PubMed] [Google Scholar]
- Jarillo, J.A., Ahmad, M., and Cashmore, A.R. (1998). NPL1 (accession No. AF053941): A second member of the NPH serine/threonine kinase family of Arabidopsis. Plant Physiol. 117, 719. [Google Scholar]
- Murashige, T., and Skoog, F. (1962). A revised medium for rapid growth and bioassays with tobacco tissue culture. Physiol. Plant. 15, 473–497. [Google Scholar]
- Schroeder, J.I., Allen, G.J., Hugouvieux, V., Kwak, J.M., and Waner, D. (2001). Guard cell signal transduction. Annu. Rev. Plant Physiol. Plant Mol. Biol. 52, 627–658. [DOI] [PubMed] [Google Scholar]
Cited by
Sorted by citations
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
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
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
“Moreover, phyA, cry2, and to a lower extent phot1 are unstable and degraded soon after activation (Clough and Viestra, 1997; Sakamoto and Briggs, 2002; Shalitin et al., 2002).”
BackgroundInfluentialFranklin, K. A. (2008) · New Phytologist · doi:10.1111/j.1469-8137.2008.02507.x · Cited by 801 · 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
In the light of stomatal opening: new insights into ‘the Watergate’
Roelfsema, M. R. G., & Hedrich, R. (2005) · New Phytologist · doi:10.1111/j.1469-8137.2005.01460.x · Cited by 545 · see citing works
Cryptochrome Structure and Signal Transduction
Lin, C., & Shalitin, D. (2003) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.54.110901.160901 · Cited by 485 · see citing works
Bantis, F., Smirnakou, S., Ouzounis, T., Κουκουνάρας, Α., Ntagkas, N., & Radoglou, K. M. (2018) · Scientia Horticulturae · doi:10.1016/j.scienta.2018.02.058 · Cited by 421 · see citing works
The multifaceted roles of FLOWERING LOCUS T in plant development
Pin, P. A., & Nilsson, O. R. (2012) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2012.02558.x · Cited by 384 · see citing works
A role for Arabidopsis cryptochromes and COP1 in the regulation of stomatal opening
Mao, J., Zhang, Y., Sang, Y., Li, Q., & Yang, H. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0501011102 · Cited by 385 · see citing works
Endo, A., Sawada, Y., Takahashi, H., Okamoto, M., Ikegami, K., Koiwai, H., Seo, M., Toyomasu, T., Mitsuhashi, W., Shinozaki, K., et al. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.116632 · Cited by 370 · see citing works
Halavaty, A. S., & Moffat, K. (2007) · Biochemistry · doi:10.1021/bi701543e · Cited by 317 · 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
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
“, 1997), but it is found associated with the plasma membrane in Arabidopsis (Sakamoto and Briggs, 2002) and other plant species (Briggs et al.”
BackgroundSelf-citationPhototropins Promote Plant Growth in Response to Blue Light in Low Light Environments
Takemiya, A., Inoue, S.-I., Doi, M., Kinoshita, T., & Shimazaki, K.-I. (2005) · The Plant Cell · doi:10.1105/tpc.104.030049 · Cited by 279 · see citing works
Light induces phenylpropanoid metabolism in Arabidopsis roots
Hemm, M. R., Rider, S. D., Ogas, J., Murry, D. J., & Chapple, C. C. S. (2004) · The Plant Journal · doi:10.1111/j.1365-313x.2004.02089.x · Cited by 276 · see citing works
Light perception in plant disease defence signalling
Karpiński, S. M., Gabryś, H., Mateo, A., Karpińska, B., & Mullineaux, P. M. (2003) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(03)00061-x · Cited by 264 · see citing works
phot1 Inhibition of ABCB19 Primes Lateral Auxin Fluxes in the Shoot Apex Required For Phototropism
Christie, J. M., Yang, H., Richter, G. L., Sullivan, S., Thomson, C. E., Lin, J., Titapiwatanakun, B., Ennis, M., Kaiserli, E., Lee, O. R., et al. (2011) · PLoS Biology · doi:10.1371/journal.pbio.1001076 · Cited by 245 · 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
Phosphorylation of BLUS1 kinase by phototropins is a primary step in stomatal opening
Takemiya, A., Sugiyama, N., Fujimoto, H., Tsutsumi, T., Yamauchi, S., Hiyama, A., Tada, Y., Christie, J. M., & Shimazaki, K.-I. (2013) · Nature Communications · doi:10.1038/ncomms3094 · Cited by 219 · 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
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
Inada, S., Ohgishi, M., Mayama, T., Okada, K., & Sakai, T. (2004) · The Plant Cell · doi:10.1105/tpc.019901 · Cited by 215 · see citing works
“In addition, although the leaves of the phot1 phot2 double mutant are curled (Kinoshita et al., 2001; Sakai et al., 2001; Sakamoto and Briggs, 2002), abnormality in that morphogenesis was not observed in rpt2-1, nph3-101, and a series of double mutants (data not shown).”
BackgroundResultInfluentialHan, X., Hyun, T. K., Zhang, M., Kumar, R., Koh, E.-J., Kang, B., Lucas, W. J., & Kim, J. (2014) · Developmental Cell · doi:10.1016/j.devcel.2013.12.008 · Cited by 211 · see citing works
“The associated expression of GSL8 and DR5 auxin responses occurred mainly in the epidermis and cortex of the apical hook and elongation zones of hypocotyl cells, where the photoreceptor PHOT1 is also localized (Sakamoto and Briggs, 2002; Wan et al., 2008).”
BackgroundLight Signaling, Root Development, and Plasticity
van Gelderen, K., Kang, C., & Pierik, R. (2017) · PLANT PHYSIOLOGY · doi:10.1104/pp.17.01079 · Cited by 211 · 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
FLOWERING LOCUS T Regulates Stomatal Opening
Kinoshita, T., Ono, N., Hayashi, Y., Morimoto, S., Nakamura, S., Soda, M., Kato, Y., Ohnishi, M., Nakano, T., Inoue, S., et al. (2011) · Current Biology · doi:10.1016/j.cub.2011.06.025 · Cited by 206 · see citing works
The signal transducing photoreceptors of plants
Franklin, K. A., Larner, V. S., & Whitelam, G. C. (2005) · The International Journal of Developmental Biology · doi:10.1387/ijdb.051989kf · Cited by 202 · see citing works
Folta, K. M., & Childers, K. S. (2008) · HortScience · doi:10.21273/hortsci.43.7.1957 · Cited by 192 · see citing works
Pedmale, U. V., & Liscum, E. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m702551200 · Cited by 169 · 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
Ueno, K., Kinoshita, T., Inoue, S., Emi, T., & Shimazaki, K. (2005) · Plant and Cell Physiology · doi:10.1093/pcp/pci104 · Cited by 183 · see citing works
Silva‐Navas, J., Moreno-Risueno, M. Á., Manzano, C., Téllez‐Robledo, B., Navarro‐Neila, S., Carrasco, V., Pollmann, S., Gallego, F. J., & del Pozo, J. C. (2015) · The Plant Cell · doi:10.1105/tpc.15.00857 · Cited by 178 · see citing works
“In roots, PHOT1 is mainly expressed in the transition zone (Sakamoto and Briggs, 2002; Wan et al., 2012), where dividing cells lose the mitotic potential and start to elongate and mature.”
BackgroundArabidopsisCryptochrome 2 Completes Its Posttranslational Life Cycle in the Nucleus
Yu, X., John Klejnot, B., Zhao, X., Shalitin, D., Maymon, M., Yang, H., Lee, J. S., Liu, X., Lopez, J., & Lin, C. (2007) · The Plant Cell · doi:10.1105/tpc.107.053017 · Cited by 165 · see citing works
Stoelzle, S., Kagawa, T., Wada, M., Hedrich, R., & Dietrich, P. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0333408100 · Cited by 159 · see citing works
Shoot phototropism in higher plants: New light through old concepts
Christie, J. M., & Murphy, A. S. (2013) · American Journal of Botany · doi:10.3732/ajb.1200340 · Cited by 152 · see citing works
“One such target is phot1 ( Roberts et al., 2011 ), which has been shown to partially relocalize away from the plasma membrane upon photoactivation ( Sakamoto and Briggs, 2002 ; Kaiserli et al., 2009 ).”
BackgroundBlue light-regulated molecular switch of Ser/Thr kinase in phototropin
Matsuoka, D., & Tokutomi, S. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0506402102 · Cited by 154 · see citing works
Phototropism: Bending towards Enlightenment
Whippo, C. W., & Hangarter, R. P. (2006) · The Plant Cell · doi:10.1105/tpc.105.039669 · Cited by 154 · see citing works
Suetsugu, N., Kagawa, T., & Wada, M. (2005) · Plant Physiology · doi:10.1104/pp.105.067371 · Cited by 153 · see citing works
Blue 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
Kinoshita, T., Emi, T., Tominaga, M., Sakamoto, K., Shigenaga, A., Doi, M., & Shimazaki, K. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.029629 · Cited by 148 · see citing works
Self-citationRoberts, D., Pedmale, U. V., Morrow, J., Sachdev, S., Lechner, E., Tang, X., Zheng, N., Hannink, M., Genschik, P., & Liscum, E. (2011) · The Plant Cell · doi:10.1105/tpc.111.087999 · Cited by 150 · see citing works
Guard Cells Integrate Light and Temperature Signals to Control Stomatal Aperture
Kostaki, K.-I., Coupel‐Ledru, A., Bonnell, V. C., Gustavsson, M., Sun, P., McLaughlin, F. J., Fraser, D. P., McLachlan, D. H., Hetherington, A. M., Dodd, A. N., et al. (2020) · PLANT PHYSIOLOGY · doi:10.1104/pp.19.01528 · Cited by 148 · see citing works
One ticket for multiple destinations: dual targeting of proteins to distinct subcellular locations
Silva-Filho, M. C. (2003) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2003.09.008 · Cited by 148 · 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
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
Physical interaction between VIVID and white collar complex regulates photoadaptation in Neurospora
Chen, C., DeMay, B. S., Gladfelter, A. S., Dunlap, J., & Loros, J. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1011190107 · Cited by 138 · see citing works
“A small fraction of PHOT1 is released to the cytoplasm from the plasma membrane (40), whereas PHOT2 becomes associated with theGolgi apparatus (39, 41).”
BackgroundProtein 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
LOV 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
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
“The phot2 mutants exhibit normal phototropism, leaf flattening, and stomatal opening (Kinoshita et al., 2001; Sakai et al., 2001; Sakamoto and Briggs, 2002; Kozuka et al., 2011) but exhibited a stronger chloroplast accumulation response than the wild type because of the defective avoidance response…”
BackgroundCorchnoy, S. B., Swartz, T. E., Lewis, J. W., Szundi, I., Briggs, W. R., & Bogomolni, R. A. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m209119200 · Cited by 133 · 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
Wan, Y., Jásik, J., Wang, L., Hao, H., Volkmann, D., Menzel, D., Mancuso, S., Baluška, F., & Lin, J. (2012) · The Plant Cell · doi:10.1105/tpc.111.094284 · Cited by 131 · see citing works
Idnurm, A., Rodríguez‐Romero, J., Corrochano, L. M., Sanz, C., Iturriaga, E. A., Eslava, A. P., & Heitman, J. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0600633103 · Cited by 131 · 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
Arabidopsis P-Glycoprotein19 Participates in the Inhibition of Gravitropism by Gravacin
Rojas‐Pierce, M., Titapiwatanakun, B., Sohn, E. J., Fang, F., Larive, C. K., Blakeslee, J. J., Cheng, Y. F., Cutler, S. R., Peer, W. A., Murphy, A. S., et al. (2007) · Chemistry & Biology · doi:10.1016/j.chembiol.2007.10.014 · Cited by 126 · see citing works
Cañamero, R. C., Bakrim, N., Bouly, J., Garay, A., Dudkin, E. E., Habricot, Y., & Ahmad, M. (2006) · Planta · doi:10.1007/s00425-006-0280-6 · Cited by 126 · see citing works
Jeong, R., Chandra‐Shekara, A. C., Roy-Barman, S., Navarre, D. A., Klessig, D. F., Kachroo, A., & Kachroo, P. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1004529107 · Cited by 124 · 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
SCAR Mediates Light-Induced Root Elongation inArabidopsisthrough Photoreceptors and Proteasomes
Dyachok, J., Zhu, L. Q., Liao, F., He, J., Huq, E., & Blancaflor, E. B. (2011) · The Plant Cell · doi:10.1105/tpc.111.088823 · Cited by 123 · see citing works
Phenotypic characterization of a photomorphogenic mutant
Fankhauser, C., & Casal, J. J. (2004) · The Plant Journal · doi:10.1111/j.1365-313x.2004.02148.x · Cited by 122 · see citing works
Structural Basis of the LOV1 Dimerization of Arabidopsis Phototropins 1 and 2
Nakasako, M., Zikihara, K., Matsuoka, D., Katsura, H., & Tokutomi, S. (2008) · Journal of Molecular Biology · doi:10.1016/j.jmb.2008.06.033 · Cited by 121 · see citing works
Time Gating of Chloroplast Autofluorescence Allows Clearer Fluorescence Imaging In Planta
Kodama, Y. (2016) · PLoS ONE · doi:10.1371/journal.pone.0152484 · Cited by 118 · see citing works
Suetsugu, N., & Wada, M. (2013) · Plant and Cell Physiology · doi:10.1093/pcp/pcs165 · Cited by 122 · 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
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
Barbosa, I. C. R., Shikata, H., Zourelidou, M., Heilmann, M., Heilmann, I., & Schwechheimer, C. (2016) · Development · doi:10.1242/dev.137117 · Cited by 104 · 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-citationNouri, M., & Komatsu, S. (2010) · PROTEOMICS · doi:10.1002/pmic.200900632 · Cited by 109 · see citing works
Root Tropisms: Investigations on Earth and in Space to Unravel Plant Growth Direction
Muthert, L. W. F., Izzo, L. G., van Zanten, M., & Aronne, G. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2019.01807 · Cited by 109 · see citing works
Wan, 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
“As shown previously (Sakamoto and Briggs, 2002), blue light induces a re-localization of PHOT1::GFP into the cytoplasm.”
BackgroundInfluentialSelf-citationGalen, C., Rabenold, J. J., & Emmanuel Liscum, A. (2006) · New Phytologist · doi:10.1111/j.1469-8137.2006.01893.x · Cited by 106 · see citing works
Lariguet, P., & Fankhauser, C. (2004) · The Plant Journal · doi:10.1111/j.1365-313x.2004.02256.x · Cited by 103 · see citing works
“After extended blue light treatments (24 h, 20 lmol m sec) phot1 protein levels are downregulated (Sakamoto and Briggs, 2002).”
BackgroundPhytochrome Cytoplasmic Signaling
Hughes, J. (2013) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-050312-120045 · Cited by 104 · see citing works
A Plant-Specific Protein Essential for Blue-Light-Induced Chloroplast Movements
DeBlasio, S. L., Luesse, D. L., & Hangarter, R. P. (2005) · Plant Physiology · doi:10.1104/pp.105.061887 · 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-citationA 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
“Went hypothesis proposes that the differential growth exhibited by a plant when illuminated with unidirectional light is a result of differential concentrations of auxin on the illuminated and shaded sides of the plant (Went and Thimann, 1937).”
BackgroundConformational Changes in a Photosensory LOV Domain Monitored by Time-Resolved NMR Spectroscopy
Harper, S. M., Neil, L. C., Day, I. J., Hore, P. J., & Gardner, K. H. (2004) · Journal of the American Chemical Society · doi:10.1021/ja038224f · Cited by 98 · see citing works
Folta, K. M., Lieg, E. J., Brooks, T. D., & Spalding, E. P. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.024372 · Cited by 96 · see citing works
“The time course of phot1 action may also be influenced by the intracellular redistribution of phot1 (release from the plasma membrane), which follows blue-light treatment (Sakamoto and Briggs, 2002).”
BackgroundBlue 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
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
Islam, S. D.-M., Penzkofer, А., & Hegemann, P. (2003) · Chemical Physics · doi:10.1016/s0301-0104(03)00187-3 · Cited by 95 · see citing works
Schwacke, R., Fischer, K., Striberny, B., Krupinska, K., & Krause, K. (2007) · Molecular Genetics and Genomics · doi:10.1007/s00438-007-0214-4 · Cited by 92 · 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
“However, upon blue light irradiation a fraction is internalized into the cytoplasm ( Sakamoto and Briggs, 2002 ; Wan et al., 2008 ; Kaiserli et al., 2009 ).”
BackgroundHan, I.-S., Tseng, T.-S., Eisinger, W., & Briggs, W. R. (2008) · The Plant Cell · doi:10.1105/tpc.108.059915 · Cited by 77 · see citing works
Self-citationInteraction 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
How and why do root apices sense light under the soil surface?
Mei, M., Yokawa, K., Wan, Y., & Baluška, F. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.00775 · Cited by 88 · see citing works
Blue light inhibits guard cell plasma membrane anion channels in a phototropin‐dependent manner
Marten, H., Hedrich, R., & Roelfsema, M. R. G. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2006.03026.x · Cited by 88 · see citing works
Evolutionary Adaptations of Plant AGC Kinases: From Light Signaling to Cell Polarity Regulation
Rademacher, E. H., & Offringa, R. (2012) · Frontiers in Plant Science · doi:10.3389/fpls.2012.00250 · Cited by 81 · 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
Protein Kinases Fpk1p and Fpk2p are Novel Regulators of Phospholipid Asymmetry
Nakano, K., Yamamoto, T. G., Kishimoto, T., Noji, T., & Tanaka, K. (2008) · Molecular Biology of the Cell · doi:10.1091/mbc.e07-07-0646 · Cited by 86 · see citing works
“Thus, NRC-2 and phototropins are implicated in membrane-associated functions, and, interestingly, both phototropin-1 and -2 are localized to the plasma membrane ( Sakamoto and Briggs, 2002 ).”
BackgroundKodama, Y., Suetsugu, N., Kong, S.-G., & Wada, M. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1007836107 · Cited by 84 · see citing works
Zhao, X., Wang, Y.-L., Qiao, X.-R., Wang, J., Wang, L.-D., Xu, C.-S., & Zhang, X. (2013) · Plant Physiology · doi:10.1104/pp.113.216556 · Cited by 84 · 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
Targeted knockout in Physcomitrella reveals direct actions of phytochrome in the cytoplasm
Mittmann, F., Brücker, G., Zeidler, M., Repp, A., Abts, T., Hartmann, E., & Hughes, J. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0403140101 · Cited by 82 · see citing works
Phytochrome A is an irradiance‐dependent red light sensor
Franklin, K. A., Allen, T., & Whitelam, G. C. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03036.x · Cited by 81 · see citing works
Skirpan, A. L., Wu, X., & McSteen, P. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2008.03546.x · Cited by 79 · see citing works
- Authors
- Sakamoto, K., & Briggs, W. R.
- Affiliations
- Carnegie Institution for Science (US)
- ORCID
- Sakamoto, Koji
- Venue
- The Plant Cell
- Publisher
- Oxford University Press (OUP)
- Published
- 2002-08
- Volume
- 14
- Issue
- 8
- Pages
- 1723-1735
- ISSN
- 1040-4651 (ISSN-L)
- 1532-298X
- PMC
- PMC151461
- OpenAlex
- W2159183165
- Cited by
- 405
- References
- 58
- Citations by year
- 2026: 4 · 2025: 5 · 2024: 14 · 2023: 10 · 2022: 15 · 2021: 12 · 2020: 16 · 2019: 10 · 2018: 12 · 2017: 14 · 2016: 14 · 2015: 15 · 2014: 20 · 2013: 21 · 2012: 28
- FWCI
- 23.65
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- The Plant Cell (publishedVersion)
- PubMed Central (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 › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Photosynthetic Processes and Mechanisms
- Keywords
- phototropin 1, subcellular localization, plasma membrane, blue light photoreception, phototropism, phot2, chloroplast movement, stomatal opening, leaf expansion, cortical cells, apical hook, root elongation zone, guard cells, vascular parenchyma, Arabidopsis thaliana
- MeSH terms
- Cell Membrane, Chloroplasts, Eye Proteins, Flavoproteins, Luminescent Proteins, Mutation, Phosphoproteins, Phosphorylation, Plasmids, Promoter Regions, Genetic, Immunoblotting, Protein Serine-Threonine Kinases, Arabidopsis, Photoreceptor Cells, Invertebrate, Gene Expression Regulation, Plant, Plant Leaves, Plant Roots, Phototropism, Hypocotyl, Plant Stems, Microscopy, Confocal, Plant Epidermis, Arabidopsis Proteins, Drosophila Proteins, Plants, Genetically Modified, Receptors, G-Protein-Coupled, Green Fluorescent Proteins, Cryptochromes
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