Modulation of Phototropic Responsiveness in Arabidopsis through Ubiquitination of Phototropin 1 by the CUL3-Ring E3 Ubiquitin Ligase CRL3NPH3

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

THE UBIQUITIN SYSTEM

Hershko, A., & Ciechanover, A. (1998) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.67.1.425 · Cited by 8,840

Improved monomeric red, orange and yellow fluorescent proteins derived from Discosoma sp. red fluorescent protein

Shaner, N. C., Campbell, R. E., Steinbach, P. A., Giepmans, B. N. G., Palmer, A. E., & Tsien, R. Y. (2004) · Nature Biotechnology · doi:10.1038/nbt1037 · Cited by 4,619

A Gateway Cloning Vector Set for High-Throughput Functional Analysis of Genes in Planta

Curtis, M. D., & Grossniklaus, U. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.027979 · Cited by 2,645

Proteasome inhibitors: valuable new tools for cell biologists.

Lee, D. H., & Goldberg, A. L. (1998) · Trends in Cell Biology · doi:10.1016/s0962-8924(98)01346-4 · Cited by 1,474

Keap1 Is a Redox-Regulated Substrate Adaptor Protein for a Cul3-Dependent Ubiquitin Ligase Complex

Zhang, D. D., Lo, S., Cross, J. V., Templeton, D. J., & Hannink, M. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.24.10941-10953.2004 · Cited by 1,284

Coordinated regulation of Arabidopsis thaliana development by light and gibberellins

Feng, S., Martínez, C., Gusmaroli, G., Wang, Y., Zhou, J., Wang, F., Chen, L., Yu, L., Iglesias‐Pedraz, J. M., Kircher, S., et al. (2008) · Nature · doi:10.1038/nature06448 · Cited by 1,118

Red fluorescent protein

CHAFFEY, N. J. (2001) · Trends in Plant Science · doi:10.1016/s1360-1385(01)01902-1 · Cited by 1,045

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

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

The emerging family of CULLIN3-RING ubiquitin ligases (CRL3s): cellular functions and disease implications

Genschik, P., Sumara, I., & Lechner, E. (2013) · The EMBO Journal · doi:10.1038/emboj.2013.173 · Cited by 278

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

Plant Strategies for Enhancing Access to Sunlight

Fiorucci, A.-S., & Fankhauser, C. (2017) · Current Biology · doi:10.1016/j.cub.2017.05.085 · Cited by 220

Plant E3 Ligases: Flexible Enzymes in a Sessile World

Chen, L., & Hellmann, H. A. (2013) · Molecular Plant · doi:10.1093/mp/sst005 · Cited by 220

Lysine 63 -linked ubiquitylation of PIN2 auxin carrier protein governs hormonally controlled adaptation of Arabidopsis root growth

Leitner, J. J., Petrášek, J., Tomanov, K., Retzer, K., Pařezová, M., Korbei, B., Bachmair, A., Zažı́malová, E., & Luschnig, C. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1200824109 · Cited by 213

PIF4 and PIF5 Transcription Factors Link Blue Light and Auxin to Regulate the Phototropic Response in Arabidopsis

Sun, J., Qi, L., Li, Y., Zhai, Q., & Li, C. (2013) · The Plant Cell · doi:10.1105/tpc.113.112417 · Cited by 180

Plant Phototropic Growth

Fankhauser, C., & Christie, J. M. (2015) · Current Biology · doi:10.1016/j.cub.2015.03.020 · Cited by 167

Activation and Polarity Control of PIN-FORMED Auxin Transporters by Phosphorylation

Barbosa, I. C. R., Hammes, U. Z., & Schwechheimer, C. (2018) · Trends in Plant Science · doi:10.1016/j.tplants.2018.03.009 · Cited by 152

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

D6PK AGCVIII Kinases Are Required for Auxin Transport and Phototropic Hypocotyl Bending in Arabidopsis

Willige, 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

Regulation of polar auxin transport by protein and lipid kinases

Armengot, L., Marquès‐Bueno, M. M., & Jaillais, Y. (2016) · Journal of Experimental Botany · doi:10.1093/jxb/erw216 · Cited by 139

The Signal Transducer NPH3 Integrates the Phototropin1 Photosensor with PIN2-Based Polar Auxin Transport in Arabidopsis Root Phototropism

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

Regulation of plant immunity through ubiquitin‐mediated modulation of Ca2+–calmodulin– A t SR 1/ CAMTA 3 signaling

Zhang, L., Du, L., Shen, C., Yang, Y., & Poovaiah, B. W. (2014) · The Plant Journal · doi:10.1111/tpj.12473 · Cited by 124

AUXOLOGY: When auxin meets plant evo-devo

Finet, C., & Jaillais, Y. (2012) · Developmental Biology · doi:10.1016/j.ydbio.2012.05.039 · Cited by 128

Recognizing the hidden half in wheat: root system attributes associated with drought tolerance

Li, C., Li, L., Reynolds, M. P., Wang, J., Chang, X., Mao, X., & Jing, R. (2021) · Journal of Experimental Botany · doi:10.1093/jxb/erab124 · Cited by 114

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

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

Phytochrome Cytoplasmic Signaling

Hughes, J. (2013) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-050312-120045 · Cited by 108

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

Proteasome-Mediated Degradation of FRIGIDA Modulates Flowering Time in Arabidopsis during Vernalization

Hu, X., Kong, X., Wang, C., Ma, L., Zhao, J., Wei, J., Zhang, X., Loake, G. J., Zhang, T., Huang, J., et al. (2014) · The Plant Cell · doi:10.1105/tpc.114.132738 · Cited by 102

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 99

Phototropism: Translating light into directional growth

Hohm, T., Preuten, T., & Fankhauser, C. (2012) · American Journal of Botany · doi:10.3732/ajb.1200299 · Cited by 96

Hemagglutinin of Influenza A Virus Antagonizes Type I Interferon (IFN) Responses by Inducing Degradation of Type I IFN Receptor 1

Xia, C., Vijayan, M., Pritzl, C. J., Fuchs, S. Y., McDermott, A. B., & Hahm, B. (2015) · Journal of Virology · doi:10.1128/jvi.02749-15 · Cited by 93

Deciphering source and sink responses of potato plants ( Solanum tuberosum L .) to elevated temperatures

Hastilestari, B. R., Lorenz, J., Reid, S., Hofmann, J., Pscheidt, D., Sonnewald, U., & Sonnewald, S. (2018) · Plant Cell & Environment · doi:10.1111/pce.13366 · Cited by 95

CUL3 E3 ligases in plant development and environmental response

Ban, Z., & Estelle, M. A. (2021) · Nature Plants · doi:10.1038/s41477-020-00833-6 · Cited by 88

Potato NPH3/RPT2-Like Protein StNRL1, Targeted by a Phytophthora infestans RXLR Effector, Is a Susceptibility Factor

Yang, L., McLellan, H., Naqvi, S., He, Q., Boevink, P. C., Armstrong, M. R., Giuliani, L. M., Zhang, W., Tian, Z., Zhan, J., et al. (2016) · PLANT PHYSIOLOGY · doi:10.1104/pp.16.00178 · Cited by 90

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 86

Multiple Routes of Light Signaling during Root Photomorphogenesis

Lee, H., Park, Y., Ha, J., Baldwin, I. T., & Park, C. (2017) · Trends in Plant Science · doi:10.1016/j.tplants.2017.06.009 · Cited by 85

Plant pathogen effector utilizes host susceptibility factor NRL1 to degrade the immune regulator SWAP70

He, Q., Naqvi, S., McLellan, H., Boevink, P. C., Champouret, N., Hein, I., & Birch, P. R. J. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1808585115 · Cited by 85

Shining Light on the Function of NPH3/RPT2-Like Proteins in Phototropin Signaling

Christie, J. M., Suetsugu, N., Sullivan, S., & Wada, M. (2018) · Plant Physiology · doi:10.1104/pp.17.00835 · Cited by 81

Proteasome‐independent functions of lysine‐63 polyubiquitination in plants

Romero-Barrios, N., & Vert, G. (2017) · New Phytologist · doi:10.1111/nph.14915 · Cited by 77

Control of Adventitious Root Architecture in Rice by Darkness, Light, and Gravity

Lin, C. Y., & Sauter, M. (2017) · PLANT PHYSIOLOGY · doi:10.1104/pp.17.01540 · Cited by 76

Regulation of plant phototropic growth by NPH3/RPT2-like substrate phosphorylation and 14-3-3 binding

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

Change your Tplate, change your fate: plant CME and beyond

Zhang, Y., Persson, S., Hirst, J., Robinson, M. S., Damme, D. V., & Sánchez‐Rodríguez, C. (2014) · Trends in Plant Science · doi:10.1016/j.tplants.2014.09.002 · Cited by 71

Arabidopsis ROOT PHOTOTROPISM2 Contributes to the Adaptation to High-Intensity Light in Phototropic Responses

Haga, K., Tsuchida-Mayama, T., Yamada, M., & Sakai, T. (2015) · The Plant Cell · doi:10.1105/tpc.15.00178 · Cited by 66

Composition, Roles, and Regulation of Cullin-Based Ubiquitin E3 Ligases

Choi, C. M., Gray, W. M., Mooney, S., & Hellmann, H. A. (2014) · The Arabidopsis Book · doi:10.1199/tab.0175 · Cited by 71

Molecular Genetic Analysis of Phototropism in Arabidopsis

Sakai, T., & Haga, K. (2012) · Plant and Cell Physiology · doi:10.1093/pcp/pcs111 · Cited by 66

Identification of Arabidopsis MYB56 as a Novel Substrate for CRL3 BPM E3 Ligases

Chen, L., Bernhardt, A., Lee, J., & Hellmann, H. A. (2015) · Molecular Plant · doi:10.1016/j.molp.2014.10.004 · Cited by 63

Phytochrome B Is Required for Systemic Stomatal Responses and Reactive Oxygen Species Signaling during Light Stress

Devireddy, A. R., Emmanuel Liscum, A., & Mittler, R. (2020) · PLANT PHYSIOLOGY · doi:10.1104/pp.20.01084 · Cited by 62

BTB domains: A structural view of evolution, multimerization, and protein–protein interactions

Bonchuk, A. N., Balagurov, K., & Georgiev, P. G. (2022) · BioEssays · doi:10.1002/bies.202200179 · Cited by 66

Phototropins maintain robust circadian oscillation of PSII operating efficiency under blue light

Litthauer, S., Battle, M. W., Lawson, T., & Jones, M. A. (2015) · The Plant Journal · doi:10.1111/tpj.12947 · Cited by 61

Posttranslational modification and trafficking of PIN auxin efflux carriers

Löfke, C., Luschnig, C., & Kleine‐Vehn, J. (2012) · Mechanisms of Development · doi:10.1016/j.mod.2012.02.003 · Cited by 61

Genome-wide identification and expression analysis of the BTB domain-containing protein gene family in tomato

Li, J., Su, X., Wang, Y., Yang, W. C., Pan, Y., Su, C., & Zhang, X. (2017) · Genes & Genomics · doi:10.1007/s13258-017-0604-x · Cited by 57

The expression of phototropins in Arabidopsis leaves: developmental and light regulation

Łabuz, J., Sztatelman, O., Banaś, A. K., & Gabryś, H. (2012) · Journal of Experimental Botany · doi:10.1093/jxb/ers061 · Cited by 56

Dynamic control of auxin transport-dependent growth by AGCVIII protein kinases

Barbosa, I. C. R., & Schwechheimer, C. (2014) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2014.09.010 · Cited by 56

MAB4-induced auxin sink generates local auxin gradients in Arabidopsis organ formation

Furutani, M., Nakano, Y., & Tasaka, M. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1316109111 · Cited by 59

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 56

Mechanism of Dual Targeting of the Phytochrome Signaling Component HEMERA/pTAC12 to Plastids and the Nucleus

Nevarez, P. A., Qiu, Y., Inoue, H., Yoo, C. Y., Benfey, P. N., Schnell, D. J., & Chen, M. (2017) · PLANT PHYSIOLOGY · doi:10.1104/pp.16.00116 · Cited by 47

Quantitative ubiquitylomics approach for characterizing the dynamic change and extensive modulation of ubiquitylation in rice seed germination

He, D., Li, M., Damaris, R. N., Bu, C., Xue, J., & Yang, P. (2019) · The Plant Journal · doi:10.1111/tpj.14593 · Cited by 46

Arabidopsis cryptochrome 1 undergoes COP1 and LRBs‐dependent degradation in response to high blue light

Miao, L., Zhao, J., Yang, G., Xu, P., Cao, X., Du, S., Xu, F., Jiang, L., Zhang, S., Wei, X., et al. (2021) · New Phytologist · doi:10.1111/nph.17695 · Cited by 43

The lowdown on breakdown: Open questions in plant proteolysis

Eckardt, N. A., Avin‐Wittenberg, T., Bassham, D. C., Chen, P., Chen, Q., Fang, J., Genschik, P., Ghifari, A. S., Guercio, A. M., Gibbs, D. J., et al. (2024) · The Plant Cell · doi:10.1093/plcell/koae193 · Cited by 47

Blue Light-Induced Proteomic Changes in Etiolated Arabidopsis Seedlings

Deng, Z., Osés-Prieto, J. A., Kutschera, U., Tseng, T., Hao, L., Burlingame, A. L., Wang, Z., & Briggs, W. R. (2014) · Journal of Proteome Research · doi:10.1021/pr500010z · Cited by 41

Genome-wide identification and transcriptome profiling reveal that E3 ubiquitin ligase genes relevant to ethylene, auxin and abscisic acid are differentially expressed in the fruits of melting flesh and stony hard peach varieties

Tan, B., Lian, X., Cheng, J., Zeng, W., Zheng, X., Wang, W., Ye, X., Li, J., Li, Z., Zhang, L., et al. (2019) · BMC Genomics · doi:10.1186/s12864-019-6258-0 · Cited by 41

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

The impact of temperature on blue light induced chloroplast movements in Arabidopsis thaliana

Łabuz, J., Hermanowicz, P., & Gabryś, H. (2015) · Plant Science · doi:10.1016/j.plantsci.2015.07.013 · Cited by 40

Dynamics in PIN2 auxin carrier ubiquitylation in gravity-responding Arabidopsis roots

Leitner, J. J., Retzer, K., Korbei, B., & Luschnig, C. (2012) · Plant Signaling & Behavior · doi:10.4161/psb.21715 · Cited by 39

Reduced phototropism in pks mutants may be due to altered auxin‐regulated gene expression or reduced lateral auxin transport

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

Lipid anchoring of A rabidopsis phototropin 1 to assess the functional significance of receptor internalization: should I stay or should I go?

Preuten, T., Blackwood, L., Christie, J. M., & Fankhauser, C. (2015) · New Phytologist · doi:10.1111/nph.13299 · Cited by 39

A C-Terminal Membrane Association Domain of Phototropin 2 is Necessary for Chloroplast Movement

Kong, S., Kagawa, T., Wada, M., & Nagatani, A. (2012) · Plant and Cell Physiology · doi:10.1093/pcp/pcs132 · Cited by 39

Zooming into plant ubiquitin-mediated endocytosis

Dubeaux, G., & Vert, G. (2017) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2017.07.005 · Cited by 36

High-Resolution Linkage Map With Allele Dosage Allows the Identification of Regions Governing Complex Traits and Apospory in Guinea Grass (Megathyrsus maximus)

Déo, T. G., Ferreira, R. C. U., Lara, L. A. C., Moraes, A. D. C. L., Alves‐Pereira, A., de Oliveira, F. A., Garcia, A. A. F., Santos, M. F., Jank, L., & de Souza, A. P. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.00015 · Cited by 36

Blue-light-activated phototropin2 trafficking from the cytoplasm to Golgi/post-Golgi vesicles

Aggarwal, C., Banaś, A. K., Kasprowicz‐Maluśki, A., Borghetti, C., Łabuz, J., Dobrucki, J. W., & Gabryś, H. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/eru172 · Cited by 35

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 33

PIN3-mediated auxin transport contributes to blue light-induced adventitious root formation in Arabidopsis

Zhai, S., Cai, W., Xiang, Z., Chen, C., Lu, Y., & Yuan, T. (2021) · Plant Science · doi:10.1016/j.plantsci.2021.111044 · Cited by 35

Deetiolation Enhances Phototropism by Modulating NON-PHOTOTROPIC HYPOCOTYL3 Phosphorylation Status

Sullivan, S., Kharshiing, E., Laird, J., Sakai, T., & Christie, J. M. (2019) · Plant Physiology · doi:10.1104/pp.19.00206 · Cited by 33

Plasma Membrane Protein Ubiquitylation and Degradation as Determinants of Positional Growth in Plants

Korbei, B., & Luschnig, C. (2013) · Journal of Integrative Plant Biology · doi:10.1111/jipb.12059 · Cited by 35

The Beginning of the End: Initial Steps in the Degradation of Plasma Membrane Proteins

Schwihla, M., & Korbei, B. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.00680 · Cited by 33

Phot2‐regulated relocation of NPH3 mediates phototropic response to high‐intensity blue light in Arabidopsis thaliana

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

Light signaling in photosynthetic eukaryotes with ‘green’ and ‘red’ chloroplasts

Lepetit, B., & Dietzel, L. (2014) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2014.07.007 · Cited by 34

Casein Kinase 1α Mediates the Degradation of Receptors for Type I and Type II Interferons Caused by Hemagglutinin of Influenza A Virus

Xia, C., Wolf, J. J., Vijayan, M., Studstill, C. J., Ma, W., & Hahm, B. (2018) · Journal of Virology · doi:10.1128/jvi.00006-18 · Cited by 34

Blue‐light receptor phototropin 1 suppresses immunity to promote Phytophthora infestans infection

Naqvi, S., He, Q., Trusch, F., Qiu, H., Pham, J., Sun, Q., Christie, J. M., Gilroy, E. M., & Birch, P. R. J. (2021) · New Phytologist · doi:10.1111/nph.17929 · Cited by 31

Physical Control Over Endocytosis

Baluška, F., & Wan, Y. (2012) · Springer eBooks · doi:10.1007/978-3-642-32463-5_6 · Cited by 31

A CULLINary ride across the secretory pathway: more than just secretion

Lu, A., & Pfeffer, S. R. (2014) · Trends in Cell Biology · doi:10.1016/j.tcb.2014.02.001 · Cited by 32

Phototropin 1 and 2 Influence Photosynthesis, UV-C Induced Photooxidative Stress Responses, and Cell Death

Rusaczonek, A., Czarnocka, W., Willems, P., Sujkowska‐Rybkowska, M., Breusegem, F. V., & Karpiński, S. M. (2021) · Cells · doi:10.3390/cells10020200 · Cited by 32

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

Phytochrome A Mediates Blue-Light Enhancement of Second-Positive Phototropism in Arabidopsis

Sullivan, S., Hart, J. E., Rasch, P., Walker, C. H., & Christie, J. M. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.00290 · Cited by 31

LsNRL4 enhances photosynthesis and decreases leaf angles in lettuce

An, G., Qi, Y., Zhang, W., Gao, H., Qian, J., Larkin, R. M., Chen, J., & Kuang, H. (2022) · Plant Biotechnology Journal · doi:10.1111/pbi.13878 · Cited by 29

Photosensory adaptation mechanisms in hypocotyl phototropism: how plants recognize the direction of a light source

Haga, K., & Sakai, T. (2023) · Journal of Experimental Botany · doi:10.1093/jxb/erad015 · Cited by 26

Both LOV1 and LOV2 domains of phototropin2 function as the photosensory domain for hypocotyl phototropic responses in Arabidopsis thaliana (Brassicaceae)

Suetsugu, N., Kong, S., Kasahara, M., & Wada, M. (2012) · American Journal of Botany · doi:10.3732/ajb.1200308 · Cited by 25

Location Matters: Canopy Light Responses over Spatial Scales

Küpers, J. J., van Gelderen, K., & Pierik, R. (2018) · Trends in Plant Science · doi:10.1016/j.tplants.2018.06.011 · Cited by 26

Arabidopsis ROOT PHOTOTROPISM2 Is a Light-Dependent Dynamic Modulator of Phototropin1

Kimura, T., Tsuchida-Mayama, T., Imai, H., Okajima, K., Ito, K., & Sakai, T. (2020) · The Plant Cell · doi:10.1105/tpc.19.00926 · Cited by 22

The Phototropic Response is Locally Regulated Within the Topmost Light-Responsive Region of the Arabidopsis thaliana Seedling

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

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

Arabidopsis G-protein β subunit AGB1 interacts with NPH3 and is involved in phototropism

Kansup, J., Tsugama, D., Liu, S., & Takano, T. (2014) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2014.01.106 · Cited by 21

Functional characterization of Arabidopsis phototropin 1 in the hypocotyl apex

Sullivan, S., Takemiya, A., Kharshiing, E. V., Cloix, C., Shimazaki, K., & Christie, J. M. (2016) · The Plant Journal · doi:10.1111/tpj.13313 · Cited by 17

The 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

Phosphorylation of NONPHOTOTROPIC HYPOCOTYL3 affects photosensory adaptation during the phototropic response

Kimura, T., Haga, K., Nomura, Y., Higaki, T., Nakagami, H., & Sakai, T. (2021) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiab281 · Cited by 15

Genome-wide identification, structural and gene expression analysis of BTB gene family in soybean

Elsanosi, H. A., Zhang, J., Mostafa, S., Geng, X., Zhou, G., Awdelseid, A. H. M., & Li, S. (2024) · BMC Plant Biology · doi:10.1186/s12870-024-05365-1 · Cited by 16

BPH1, a novel substrate receptor of CRL3, plays a repressive role in ABA signal transduction

Woo, O.-G., Kim, S.-H., Cho, S. K., Kim, S. H., Lee, H. N., Chung, T., Yang, S. W., & Lee, J. (2018) · Plant Molecular Biology · doi:10.1007/s11103-018-0717-x · Cited by 15

A MUB E2 structure reveals E1 selectivity between cognate ubiquitin E2s in eukaryotes

Lu, X., Malley, K. R., Brenner, C., Koroleva, O., Korolev, S., & Downes, B. P. (2016) · Nature Communications · doi:10.1038/ncomms12580 · Cited by 14

OsBTBZ1 Confers Salt Stress Tolerance in Arabidopsis thaliana

Saputro, T. B., Jakada, B. H., Chutimanukul, P., Comai, L., Buaboocha, T., & Chadchawan, S. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241914483 · Cited by 13

The nonphototrophic hypocotyl 3 (NPH3) domain protein NRL5 is a trafficking-associated GTPase essential for drought resistance

Upadhyay, N., Huang, X., Lee, Y., Singh, S. K., Hsu, C., Huang, S.-S., & Verslues, P. E. (2024) · Science Advances · doi:10.1126/sciadv.ado5429 · Cited by 12

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

Auxin and Tropisms

Retzer, K., Korbei, B., & Luschnig, C. (2014) · Springer eBooks · doi:10.1007/978-3-7091-1526-8_16 · Cited by 13

Light signaling as cellular integrator of multiple environmental cues in plants

Kanojia, A., Bhola, D., & Mudgil, Y. (2023) · Physiology and Molecular Biology of Plants · doi:10.1007/s12298-023-01364-y · Cited by 13

Emerging Role of the Ubiquitin Proteasome System in the Control of Shoot Apical Meristem FunctionF

Giacomo, E. D., Serino, G., & Frugis, G. (2012) · Journal of Integrative Plant Biology · doi:10.1111/jipb.12010 · Cited by 11

Genome-Wide Characterization of the BTB Gene Family in Poplar and Expression Analysis in Response to Hormones and Biotic/Abiotic Stresses

Yue, J., Dai, X., Li, Q., & Wei, M. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25169048 · Cited by 9

Phototropin Interactions with SUMO Proteins

Łabuz, J., Sztatelman, O., Jagiełło-Flasińska, D., Hermanowicz, P., Bażant, A., Banaś, A. K., Bartnicki, F., Giza, A., Kozłowska, A., Lasok, H., et al. (2021) · Plant and Cell Physiology · doi:10.1093/pcp/pcab027 · Cited by 9

The Roles of Cullins E3 Ubiquitin Ligases in the Lipid Biosynthesis of the Green Microalgae Chlamydomonas reinhardtii

Luo, Q., Zou, X., Wang, C., Li, Y., & Hu, Z. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094695 · Cited by 9

Analysis of post-translational modifications of the blue light photoreceptor, phot1, by the CRL3NPH3 ubiquitin ligase complex

Roberts, D. R. (2013) · doi:10.32469/10355/37805 · Cited by 1

Regulation of Phototropic Signaling in Arabidopsis via Phosphorylation State Changes in the Phototropin 1-interacting Protein NPH3

Pedmale, U. V., & Liscum, E. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m702551200 · Cited by 169

Mechanisms of the phototropic pathway

Morrow, J. (2018) · doi:10.32469/10355/69866

Phot2‐regulated relocation of NPH3 mediates phototropic response to high‐intensity blue light in Arabidopsis thaliana

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

The phosphorylation status of NONPHOTOTROPIC HYPOCOTYL3 affects phot2-dependent phototropism in Arabidopsis

Kimura, T., Haga, K., & Sakai, T. (2022) · Plant Signaling & Behavior · doi:10.1080/15592324.2022.2027138 · Cited by 6