Cited by 785Light effects on plantsPlant Molecular Biology ResearchPhotosynthetic Processes and Mechanisms

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Phototropins 1 and 2: versatile plant blue-light receptors

Briggs, Winslow R., Christie, John M.·2002·Trends in Plant Science

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Abstract

Blue and ultraviolet-A light regulate a wide range of responses in plants, including phototropism, chloroplast migration and stomatal opening. However, the photoreceptors for these light responses have been identified only recently. The phototropins (phot1 and phot2) represent a new class of receptor kinases that appear to be exclusive to plants. Recent genetic analysis has shown that phot1 and phot2 exhibit partially overlapping functions in mediating phototropism, chloroplast migration, and stomatal opening in Arabidopsis. Although significant progress has been made in understanding the early photochemical and biochemical events that follow phototropin excitation, the details of how this excitation activates such different responses remain to be elucidated.

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The eukaryotic protein kinase superfamily: kinase (catalytic) domain structure and classification 1
Hanks, S. K., & Hunter, T. (1995) · The FASEB Journal · doi:10.1096/fasebj.9.8.7768349 · Cited by 2,828
Protein kinases 6. The eukaryotic protein kinase superfamily: kinase (catalytic) domain structure and classification.
Hanks, S. K., & Hunter, T. R. (1995) · PubMed · Cited by 2,518
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
The 'Power of movement in plants.'--1880.
Darwin, C. R., & Darwin, F. (1880) · Cambridge University Press eBooks · doi:10.1017/cbo9780511693670 · Cited by 1,619
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
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
Arabidopsis nph1 and npl1: Blue light receptors that mediate both phototropism and chloroplast relocation
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
Self-citation
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
Self-citation
Arabidopsis NPL1: A Phototropin Homolog Controlling the Chloroplast High-Light Avoidance Response
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
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
Self-citation

Show all 74 references

Research works printed but not linked: 1

Jarillo, 1998, NPL1 (accession no. AF053941): a second member of the NPH serine/threonine kinase family of Arabidopsis, Plant Physiol., 117, 719

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“01 μmol m−2 s−1 ~ 1 μmol m−2 s−1) and high-fluence blue light (> 1 μmol m−2 s−1), including the first and second positive phototropisms, whereas PHOT2 only mediates second positive phototropism induced by high-fluence blue light (Sakai et al., 2001; Briggs and Christie, 2002).”
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“Under strong light conditions, however, chloroplasts rearrange themselves parallel to the direction of the light source so as to minimize photo-damage (Briggs and Christie 2002; Kasahara and others 2004).”
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“Plants use light as a cue for almost every physiological process including, but not limited to, seedling development, photosynthesis, growth, and budding (Briggs and Christie, 2002; Takemiya et al., 2005; Bennie et al., 2016; Gaston et al., 2017; Singhal et al., 2018).”
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“chromes (Phys) [9,10], ultraviolet (UV)-A/blue light photoreceptor cryptochromes (CRYs) [11], blue light receptor phototropins (Phots) [12,13], blue light”
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“In the AGC VIIIb subfamily, UCN and UCNL redundantly regulate planar growth of integuments, and PHOT1/2, two blue light receptors, control phototropism and chloroplast relocation (Briggs and Christie, 2002; Enugutti et al., 2012).”
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“White and blue lights cause negative phototropism and are perceived by the photoreceptor PHOTOTROPIN 1 (Phot1) expressed in the elongation zone of the root (Briggs & Christie, 2002; Liscum & Briggs, 1995; Sakamoto & Briggs, 2002).”
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“Its induction by cell deformation (activation of mechano-sensitive stretch-activated channels) and ABA treatment is plausible and the same photoreceptors (phototropin 1 and 2) have been found for controlling of chloroplasts and stomata movements (Briggs and Christie 2002).”
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Unique temperature dependence in the adduct formation between FMN and cysteine S-H group in the LOV2 domain of Adiantum phytochrome3
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“In higher plants, cryptochromes are involved in the regulation of circadian rhythms, the inhibition of hypocotyl elongation, cotyledon expansion and the transition to flowering, while phototropins are involved in phototropism, chloroplast migration and stomatal opening (Malakhov and Bowler 2001; Briggs and Christie 20…”
Background
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“2013; Briggs and Christie 2002, 1999; Christie 2007; Frank and Cogdell 1996; Kopsell and Sams 2013; Lichtenthaler 1987).”
Background
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“pigments, the cryptochrome and the phototropins (45).”
Photoinduced Oligomerization of Arabidopsis thaliana Phototropin 2 LOV1
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Absorption and emission spectroscopic characterisation of 8-amino-riboflavin
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“The principal roles of phototropins include phototropism and chloroplast movement in leaves (Briggs and Christie 2002; Cho et al. 2007), and the cryptochromes function in photomorphogenesis and the entrainment of circadian rhythms (Cashmore 2003; Endo et al.”
Background

Authors: Briggs, W. R., & Christie, J. M.
Affiliations: Carnegie Institution for Science (US)
Corresponding author: Briggs, Winslow R.
ORCID: Christie, John M.
Venue: Trends in Plant Science
Publisher: Elsevier BV
Published: 2002-05
Volume: 7
Issue: 5
Pages: 204-210
ISSN: 1360-1385 (ISSN-L)
DOI: 10.1016/s1360-1385(02)02245-8
OpenAlex: W2079139285
Cited by: 785
References: 74
Citations by year: 2026: 23 · 2025: 34 · 2024: 24 · 2023: 20 · 2022: 22 · 2021: 38 · 2020: 28 · 2019: 34 · 2018: 28 · 2017: 30 · 2016: 29 · 2015: 21 · 2014: 33 · 2013: 26 · 2012: 24
FWCI: 4.83
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Trends in Plant Science (publishedVersion)
PubMed (publishedVersion)
ENLIGHTEN (Jurnal Bimbingan dan Konseling Islam) (submittedVersion)
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 receptor, receptor kinases, phototropism, stomatal opening, UVA, Arabidopsis thaliana, photoreceptor signaling
MeSH terms: Chloroplasts, Eye Proteins, Flavoproteins, Light, Mutation, Oxygen, Phosphoproteins, Plants, Spectrophotometry, Ultraviolet Rays, Protein Serine-Threonine Kinases, Arabidopsis, Photoreceptor Cells, Invertebrate, Phototropism, Arabidopsis Proteins, Drosophila Proteins, Receptors, G-Protein-Coupled, Cryptochromes

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Phototropins 1 and 2: versatile plant blue-light receptors

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