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phot1 and phot2 mediate blue light regulation of stomatal opening
Abstract
The stomatal pores of higher plants allow for gaseous exchange into and out of leaves. Situated in the epidermis, they are surrounded by a pair of guard cells which control their opening in response to many environmental stimuli, including blue light. Opening of the pores is mediated by K(+) accumulation in guard cells through a K(+) channel and driven by an inside-negative electrical potential. Blue light causes phosphorylation and activation of the plasma membrane H(+)-ATPase that creates this potential. Thus far, no blue light receptor mediating stomatal opening has been identified, although the carotenoid, zeaxanthin, has been proposed. Arabidopsis mutants deficient in specific blue-light-mediated responses have identified four blue light receptors, cryptochrome 1 (cry1), cryptochrome 2 (cry2), phot1 and phot2. Here we show that in a double mutant of phot1 and phot2 stomata do not respond to blue light although single mutants are phenotypically normal. These results demonstrate that phot1 and phot2 act redundantly as blue light receptors mediating stomatal opening.
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“Stomatal opening is regulated by the functional redundancy of PHOT1 and PHOT2”
From The action of enhancing weak light capture via phototropic growth and chloroplast movement in plants (2022) · cites this paper as Kinoshita et al., 2001
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“phot2 mutant plants showed a slight defect in stomatal opening (Kinoshita et al., 2001), but this defect was less than that in phot1 mutant plants and was negligible in the strong light conditions used by Kasahara et al.”
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“Plants were grown in soil under a 16-h fluorescent light (50 µmol m−2 s−1)/8-h dark cycle at 24◦C at a relative humidity of 55–75% for 4–6 weeks in a dedicated growth room (Kinoshita et al., 2001).”
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“Phototropins also mediate other phenomena, such as phototropism and stomata opening (Christie et al. 1998; Kinoshita et al. 2001).”
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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
“phot was revealed to mediate chloroplast relocation movements (12–14), stomata opening (15), leaf expansion (16) and rapid inhibition of hypocotyls growth (17).”
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Effect of elevated CO2 and spectral quality on whole plant gas exchange patterns in tomatoes
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Nitric oxide inhibits blue light-induced stomatal opening by regulating the K+ influx in guard cells
Zhao, X., Qiao, X.-R., Yuan, J., Ma, X.-F., & Zhang, X. (2011) · Plant Science · doi:10.1016/j.plantsci.2011.12.007 · Cited by 33
“Since BL-specific stimulation of stomatal opening in Arabidopsis s initiated by phototropins [3], we predicted that phototropins may e involved in BL-activated inward rectifying K+ channels.”
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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 34
“…leads to H+-ATPase activation via BLUS1 kinase activity, as well as the involvement of BLUE LIGHTDEPENDENT H+-ATPASE PHOSPHORYLATION (BHP) and type 1 protein phosphatases (Kinoshita et al., 2001; Take- miya et al., 2006; Inoue et al., 2008b; Takemiya et al., 2013; Hayashi et al., 2017).”
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“Stomatal aperture in epidermal tissues was measured as described previously (Kinoshita et al., 2001; Inoue et al., 2008) with minor modifications.”
Self-citationKottke, T., Hegemann, P., Dick, B., & Heberle, J. (2006) · Biopolymers · doi:10.1002/bip.20510 · Cited by 32
Formisano, L., Miras‐Moreno, B., Ciriello, M., Zhang, L., Pascale, S. D., Lucini, L., & Rouphael, Y. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.890830 · Cited by 31
Elevated CO 2 induces rapid dephosphorylation of plasma membrane H + ‐ ATPase in guard cells
Ando, E., Kollist, H., Fukatsu, K., Kinoshita, T., & Terashima, I. (2022) · New Phytologist · doi:10.1111/nph.18472 · Cited by 31
“In guard cells, phototropins mediate phosphorylation of penultimate C-terminal residue of plasma membrane (PM) H+-ATPase, threonine (Thr), which recruits regulatory protein 14-3-3 to activate this enzyme (Kinoshita & Shimazaki, 1999, 2002; Kinoshita et al., 2001).”
BackgroundSelf-citationTransitions of gene expression induced by short‐term blue light
Lehmann, P., Nöthen, J., von Braun, S. S., Bohnsack, M. T., Mirus, O., & Schleiff, E. (2010) · Plant Biology · doi:10.1111/j.1438-8677.2010.00377.x · Cited by 31
AGCVIII kinases: at the crossroads of cellular signaling
Zhang, Y., & McCormick, S. M. (2009) · Trends in Plant Science · doi:10.1016/j.tplants.2009.09.006 · Cited by 31
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“A recent study with Arabidopsis thaliana revealed engagement of photropin 1 (phot1) and phototropin 2 (phot2) flavin proteins in photosensing ( Kinoshita et al. 2001 ).”
BackgroundRusaczonek, A., Czarnocka, W., Willems, P., Sujkowska‐Rybkowska, M., Breusegem, F. V., & Karpiński, S. M. (2021) · Cells · doi:10.3390/cells10020200 · Cited by 32
“Arabidopsis possesses two phototropins, phot1 and phot2, that share functional redundancy in processes such as chloroplast accumulation and phototropism control [14], stomata opening [15,16], leaf expansion [17], and leaf positioning [18].”
BackgroundUV Radiation Induces Specific Changes in the Carotenoid Profile of Arabidopsis thaliana
Badmus, U. O., Crestani, G., Cunningham, N., Havaux, M., Urban, O., & Jansen, M. A. K. (2022) · Biomolecules · doi:10.3390/biom12121879 · Cited by 30
“These include the UV-B photoreceptor mutant uvr8 [51], the cryptochrome double mutant cry1cry2 [52], and the phototropin double mutant phot1phot2 [53].”
BackgroundPIF transcriptional regulators are required for rhythmic stomatal movements
Rovira, A., Veciana, N., Basté-Miquel, A., Quevedo, M., Locascio, A., Yenush, L., Toledo‐Ortiz, G., Leivar, P., & Monte, E. (2024) · Nature Communications · doi:10.1038/s41467-024-48669-4 · Cited by 30
“This pathway involves the phototropin photoreceptors, which are activated via autophosphorylation under blue light 32 .”
Lima, V. F., dos Anjos, L., Medeiros, D. B., Cândido-Sobrinho, S. A., de Souza, L. P., Gago, J., Fernie, A. R., & Daloso, D. M. (2019) · New Phytologist · doi:10.1111/nph.15927 · Cited by 30
“Blue light is directly sensed by guard cell phototropins, which induce the phosphorylation of plasma membrane H+-ATPases, the degradation of starch and lipids and the accumulation of osmolytes within guard cells (Kinoshita et al., 2001; Horrer et al., 2016; McLachlan et al., 2016).”
BackgroundCircadian Rhythms in Stomata: Physiological and Molecular Aspects
Hubbard, K., & Webb, A. A. R. (2015) · Springer eBooks · doi:10.1007/978-3-319-20517-5_9 · Cited by 30
“Circadian-regulated transcripts include (1) PHOTOTROPIN1, which is involved in blue light perception for stomatal opening (Kinoshita et al. 2001), (2) ARABIDOPSIS MULTIDRUG RESISTANCE-RELATED PROTEIN 5 (AtMRP5), an ABC transporter that is expressed in guard cells and is thought to regulate closure in response to ABA,…”
BackgroundCell physiological aspects of the plasma membrane electrogenic H + pump
Tazawa, M. (2003) · Journal of Plant Research · doi:10.1007/s10265-003-0109-3 · Cited by 30
“Thus, both phot1 and phot2 are necessary for the perception of blue light as the first step of signal transduction leading to an activation of the H-ATPase (Kinoshita et al. 2001).”
Expression of Enzymes Involved in Chlorophyll Catabolism in Arabidopsis Is Light Controlled
Banaś, A. K., Łabuz, J., Sztatelman, O., Gabryś, H., & Fiedor, L. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.185504 · Cited by 32
“In contrast, the main activity of phototropins lies in the regulation of movement (Jarillo et al., 2001; Kinoshita et al., 2001; Sakai et al., 2001).”
BackgroundFunctional characterization of GhPHOT2 in chloroplast avoidance of Gossypium hirsutum
Shang, B., Zang, Y., Zhao, X., Zhu, J., Fan, C., Guo, X., & Zhang, X. (2018) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2018.11.027 · Cited by 30
“The Arabidopsis Col-0 ecotype was used as wild-type (WT), and the phot2 and phot1 phot2 mutants were described previously (Kinoshita et al., 2001).”
MethodAihara, Y., Maeda, B., Goto, K., Takahashi, K. U., Nomoto, M., Toh, S., Ye, W., Toda, Y., Uchida, M., Asai, E., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-38102-7 · Cited by 29
“…receptor kinases, phototropins, the signal is transmittedtoseveralkinases(BLUS1andBHP)andphosphatase(PP1), resulting inphosphorylation of a penultimate residue, threonine (Thr), in the C-terminus of PM H + -ATPaseand binding of 14-3-3 proteinto the phosphorylated C-terminus for activation 3,5,6 .”
Self-citationBlue radiation stimulates photosynthetic induction in Fagus sylvatica L.
Košvancová, M., Urban, O., Navrátil, M., Špunda, V., Robson, T. M., & Marek, M. V. (2009) · Photosynthetica · doi:10.1007/s11099-009-0060-1 · Cited by 29
“At low PFDs [below 15 μmol(photon) m–2 s–1], stomata only open in response to B, while R radiation has no effect (Zeiger et al. 1981, Zeiger 1986, Kinoshita et al. 2001).”
BackgroundMunekage, Y. N., INOUE, S., Yoneda, Y., & Yokota, A. (2014) · Plant Cell & Environment · doi:10.1111/pce.12466 · Cited by 29
“PHOT has been reported to mediate multiple plant responses including phototropism, chloroplast relocation, stomatal opening and leaf flattening (Huala et al. 1997; Kagawa et al. 2001; Kinoshita et al. 2001; Sakamoto & Briggs 2002; Kozuka et al. 2013).”
BackgroundTurc, B., Sahay, S., Haupt, J., Santos, T. D. O., Bai, G., & Głowacka, K. (2024) · Journal of Experimental Botany · doi:10.1093/jxb/erae113 · Cited by 28
Lighting the path: how light signaling regulates stomatal movement and plant immunity
Singh, N. P., Giri, M. K., & Chattopadhyay, D. (2024) · Journal of Experimental Botany · doi:10.1093/jxb/erae475 · Cited by 29
Light-induced systemic resistance in tomato plants against root-knot nematode Meloidogyne incognita
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“However, we could not exclude the possibility that B light induced a long-term effect on the stomatal opening (Frechilla et al. 2000; Kinoshita et al. 2001).”
BackgroundOide, M., Okajima, K., Nakagami, H., Kato, T., Sekiguchi, Y., Oroguchi, T., Hikima, T., Yamamoto, M., & Nakasako, M. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.ra117.000324 · Cited by 29
“In land plants, phototropism (3, 4), chloroplast movement (5, 6), stomata opening (7), and leaf expansion (8) are known as photomediated responses.”
BackgroundBlue Light Regulates Phosphate Deficiency-Dependent Primary Root Growth Inhibition in Arabidopsis
Yeh, C., Kobayashi, K., Fujii, S., Fukaki, H., Mitsuda, N., & Ohme‐Takagi, M. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2019.01803 · Cited by 28
“To further confirm this finding, the B light receptor mutants, cry1 cry2 and phot1 phot2, were examined under Pi deficiency (Fankhauser and Chory, 1999; Kinoshita et al., 2001).”
BackgroundVibrational Assignment of the Flavin−Cysteinyl Adduct in a Signaling State of the LOV Domain in FKF1
Kikuchi, S., Unno, M., Zikihara, K., Tokutomi, S., & Yamauchi, S. (2009) · The Journal of Physical Chemistry B · doi:10.1021/jp808399f · Cited by 27
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“PHOT2 which are receptors for the blue light regulates stomatal opening in guard cells of Arabidopsis (Kinoshita et al. 2001).”
BLUE/UV-A RECEPTORS: HISTORICAL OVERVIEW
Briggs, W. R. (2006) · Springer eBooks · doi:10.1007/1-4020-3811-9_10 · Cited by 28
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“Flavin-binding phototropins appear to have been confirmed as the principal photoreceptors in the guard cell response to BL (Kinoshita et al. 2001).”
Phototropins and Associated Signaling: Providing the Power of Movement in Higher Plants¶
Celaya, R. B., & Emmanuel Liscum, A. (2005) · Photochemistry and Photobiology · doi:10.1562/2004-08-22-ir-282.1 · Cited by 28
Arabidopsis ROOT PHOTOTROPISM2 Is a Light-Dependent Dynamic Modulator of Phototropin1
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The blue-light receptor CRY1 serves as a switch to balance photosynthesis and plant defense
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“Since its identification, phototropin has been found to mediate chloroplast relocation [4], stomatal opening [5], and leaf expansion [6] to optimise the efficiency of photosynthesis.”
BackgroundStomata Prioritize Their Responses to Multiple Biotic and Abiotic Signal Inputs
Ou, X., Gan, Y., Chen, P., Qiu, M., Jiang, K., & Wang, G. (2014) · PLoS ONE · doi:10.1371/journal.pone.0101587 · Cited by 27
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“These PHOTs regulate not only chloroplast movement, but also stomatal opening (Huala et al. 1997; Kinoshita et al. 2001) and stem phototropic curvature (Sakai et al. 2001).”
BackgroundIsolation and stomatal opening activity of two oxylipins from Ipomoea tricolor
Ohashi, T., Ito, Y., Okada, M., & Sakagami, Y. (2004) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2004.10.088 · Cited by 27
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Self-citationEffect of extremely low-frequency magnetic fields on light-induced electric reactions in wheat
Grinberg, M. A., Mudrilov, M., Kozlova, E. E., Sukhov, V., Sarafanov, F. G., Evtushenko, A. A., Ilin, N. V., Vodeneev, V., Price, C. G., & Mareev, E. A. (2022) · Plant Signaling & Behavior · doi:10.1080/15592324.2021.2021664 · Cited by 26
“39,40 Field perception by the cryptochromes occurs via light-driven charge separation on the cofactor of the enzyme, flavin adenine dinucleotide (FAD) followed by electron uptake by oxygen.”
BackgroundLanoue, J., Little, C., Hawley, D., & Hao, X. (2022) · Scientia Horticulturae · doi:10.1016/j.scienta.2022.111350 · Cited by 27
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Self-citationLight and auxin signaling cross-talk programme root development in plants
Kumari, S., & Panigrahi, K. C. S. (2019) · Journal of Biosciences · doi:10.1007/s12038-018-9838-2 · Cited by 26
“Blue light also causes stomatal opening, where both PHOT1 and PHOT2 are involved (Kinoshita et al. 2001).”
Stability of Dimer and Domain–Domain Interaction of Arabidopsis Phototropin 1 LOV2
Nakasone, Y., Eitoku, T., Zikihara, K., Matsuoka, D., Tokutomi, S., & Terazima, M. (2008) · Journal of Molecular Biology · doi:10.1016/j.jmb.2008.08.074 · Cited by 26
Impact of climate-driven changes in temperature on stomatal anatomy and physiology
Hofmann, T. A., Atkinson, W., Fan, M.-J., Simkin, A. J., Jindal, P., & Lawson, T. (2025) · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · doi:10.1098/rstb.2024.0244 · Cited by 24
“[105] suggested that full stomatal opening at high temperature requires blue light and involves phototropin photoreceptors, with only partial reliance on their downstream target BLUE LIGHT SIGNALING1 (BLUS1; [106,107]), as well as plasma membrane (PM) H + -ATPase activity [105].”
Sun, X., Kang, X., & Ni, M. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002674 · Cited by 25
“Phots regulate blue light-induced plant movements such as phototropism [5], chloroplast movement [6], and stomatal opening [7].”
BackgroundTakayama, Y., Nakasako, M., Okajima, K., Iwata, A., Kashojiya, S., Matsui, Y., & Tokutomi, S. (2011) · Biochemistry · doi:10.1021/bi101689b · Cited by 26
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Cysteinyl radicals in chemical synthesis and in nature
McLean, J. T., Benny, A., Nolan, M. D., Swinand, G., & Scanlan, E. M. (2021) · Chemical Society Reviews · doi:10.1039/d1cs00254f · Cited by 26
Controlling the Gate: The Functions of the Cytoskeleton in Stomatal Movement
Li, Y., Zhang, X., Zhang, Y., & Ren, H. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.849729 · Cited by 25
“…the H+-ATPase Frontiers in Plant Science | www.frontiersin.org 2 February 2022 | Volume 13 | Article 849729 AHA1 is activated by blue light, which leads to hyperpolarization of the plasma membrane in guard cells (Kinoshita and Shimazaki, 1999; Kinoshita et al., 2001; Hayashi et al., 2011).”
BackgroundAarabi, F., Ghigi, A., Ahchige, M. W., Bulut, M., Geigenberger, P., Neuhaus, H. E., Sampathkumar, A., Alseekh, S., & Fernie, A. R. (2023) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiad323 · Cited by 25
“…been deci-phered in multiple signaling processes, such as blue light-mediated signaling of plant tropism, chloroplast movement, and stomatal opening (Kinoshita et al. 2001; Pedmale and Liscum 2007; Demarsy et al. 2012; Kong and Wada 2016), the molecular function of PLP proteins remained elusive.”
BackgroundTan, Y., Qin, Y., Li, Y., Li, M., & Ma, F. (2014) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-014-0563-8 · Cited by 25
Plant nuclear photorelocation movement
Higa, T., Suetsugu, N., & Wada, M. (2013) · Journal of Experimental Botany · doi:10.1093/jxb/ert414 · Cited by 26
“An actin filament inhibitor cytochalasin B abrogated both tip growth and nuclear movement whereas a microtubule inhibitor colchicine attenuated tip growth and induced the basipetal movement of the nucleus (Kadota and Wada, 1995).”
BackgroundSelf-citationFunctional characterization of a constitutively active kinase variant of Arabidopsis phototropin 1
Petersen, J., Inoue, S., Kelly, S. M., Sullivan, S., Kinoshita, T., & Christie, J. M. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.799643 · Cited by 25
“Phots also optimize photosynthesis by regulating stomatal opening in response to blue light (51).”
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Functional characterization of Ostreococcus tauri phototropin
Sullivan, S., Petersen, J., Blackwood, L., Papanatsiou, M., & Christie, J. M. (2015) · New Phytologist · doi:10.1111/nph.13640 · Cited by 24
Toh, S., Takata, N., Ando, E., Toda, Y., Wang, Y., Hayashi, Y., Mitsuda, N., Nagano, S., Taniguchi, T., & Kinoshita, T. (2021) · Frontiers in Plant Science · doi:10.3389/fpls.2021.766037 · Cited by 24
Self-citationChloroplast Photorelocation Movement
Suetsugu, N., & Wada, M. (2008) · Plant cell monographs · doi:10.1007/7089_2008_34 · Cited by 28
Self-citationMolecular Evolution and Interaction of Membrane Transport and Photoreception in Plants
Babla, M. H., Cai, S., Chen, G. J., Tissue, D. T., Cazzonelli, C. I., & Chen, Z. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2019.00956 · Cited by 25
“When guard cells are illuminated with blue light, PHOTs are triggered through auto-phosphorylation for the initiation of signaling for stomatal opening (Kinoshita et al., 2001; Christie, 2007).”
Jain, M., Sharma, P., Tyagi, S. B., Tyagi, A. K., & Khurana, J. P. (2006) · Plant Science · doi:10.1016/j.plantsci.2006.08.003 · Cited by 24
Gabryś, H. (2004) · Acta Physiologiae Plantarum · doi:10.1007/s11738-004-0038-3 · Cited by 24
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Signalling mechanism of phototropin-mediated chloroplast movement in Arabidopsis
Suetsugu, N., & Wada, M. (2020) · Journal of Plant Biochemistry and Biotechnology · doi:10.1007/s13562-020-00594-5 · Cited by 23
Self-citationSharma, S., Sanyal, S. K., Sushmita, K., Chauhan, M., Sharma, A. S., Anirudhan, G., Veetil, S. K., & Kateriya, S. (2021) · Current Genomics · doi:10.2174/1389202922666210412104817 · Cited by 22
“mulation of photosystem proteins, root phototropism [64,69,71]”
BackgroundInfluentialIlluminating plant water dynamics: the role of light in leaf hydraulic regulation
Grunwald, Y., Yaaran, A., & Moshelion, M. (2023) · New Phytologist · doi:10.1111/nph.19497 · Cited by 23
Mechanical advantage makes stomatal opening speed a function of evaporative demand
Pichaco, J., Manandhar, A., & McAdam, S. A. M. (2024) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiae023 · Cited by 23
The functional domains of the chloroplast unusual positioning protein 1
Lehmann, P., Bohnsack, M. T., & Schleiff, E. (2011) · Plant Science · doi:10.1016/j.plantsci.2011.01.006 · Cited by 23
Diverse Responses to Blue Light via LOV Photoreceptors
Shimazaki, K.-I., & Tokutomi, S. (2013) · Plant and Cell Physiology · doi:10.1093/pcp/pcs172 · Cited by 23
Self-citationRegulation of stomatal opening and histone modification by photoperiod in Arabidopsis thaliana
Aoki, S., Toh, S., Nakamichi, N., Hayashi, Y., Wang, Y., Suzuki, T., Tsuji, H., & Kinoshita, T. (2019) · Scientific Reports · doi:10.1038/s41598-019-46440-0 · Cited by 23
Self-citationChloroplast movement: dissection of events downstream of photo- and mechano-perception
Sato, Y., Kadota, A., & Wada, M. (2003) · Journal of Plant Research · doi:10.1007/s10265-002-0073-3 · Cited by 22
Self-citationGoh, C., Jang, S., Jung, S., Kim, H.-S., Kang, H., Park, Y., Bae, H., Lee, C.-H., & An, G. (2008) · Plant Molecular Biology · doi:10.1007/s11103-008-9442-1 · Cited by 24
“These proteins mediate BL responses in a redundant manner (Kinoshita et al. 2001; Sakamoto and Briggs 2002; Doi et al. 2004) and have recently been implicated in growth promotion under low intensity BL conditions (Takemiya et al.”
BackgroundIsolation of a Protein Interacting with Vfphot1a in Guard Cells of Vicia faba
Emi, T., Kinoshita, T., Sakamoto, K., Mineyuki, Y., & Shimazaki, K. (2005) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.052639 · Cited by 23
“Such responses are mediated by a newly identified class of blue light receptors, phototropins (Huala et al., 1997; Christie et al., 1998; Kagawa et al., 2001; Kinoshita et al., 2001; Sakai et al., 2001).”
BackgroundSelf-citationAbscisic Acid Synthesis, Metabolism and Signal Transduction
Marion‐Poll, A., & Leung, J. (2006) · Wiley eBooks · doi:10.1002/9780470988800.ch1 · Cited by 25
Taylor, G., Walter, J., & Kromdijk, J. (2024) · Journal of Experimental Botany · doi:10.1093/jxb/erae093 · Cited by 22
Metadata
- Authors
- Kinoshita, T., Doi, M., Suetsugu, N., Kagawa, T., Wada, M., & Shimazaki, K.-I.
- Affiliations
- Kyushu University (JP)
- National Institute for Basic Biology (JP)
- Corresponding author
- Shimazaki, Ken-ichiro
- Venue
- Nature
- Published
- 2001-12
- Volume
- 414
- Issue
- 6864
- Pages
- 656-660
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2036131768
- Cited by
- 899
- References
- 31
- Citations by year
- 2026: 24 · 2025: 27 · 2024: 45 · 2023: 31 · 2022: 43 · 2021: 42 · 2020: 40 · 2019: 42 · 2018: 40 · 2017: 33 · 2016: 37 · 2015: 34 · 2014: 43 · 2013: 33 · 2012: 42
- FWCI
- 45.17
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Light effects on plants
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Photosynthetic Processes and Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Photoreceptor and optogenetics research
- Keywords
- phot1, phot2, blue light receptor, stomatal opening, guard cells, Arabidopsis thaliana, cryptochrome, plasma membrane H+-ATPase, potassium accumulation, zeaxanthin, phototropism
- MeSH terms
- Cell Membrane, Proton-Translocating ATPases, Light, Mutation, Phosphoproteins, Protein Serine-Threonine Kinases, Arabidopsis, Plant Epidermis, Reverse Transcriptase Polymerase Chain Reaction, Arabidopsis Proteins, Photosynthetic Reaction Center Complex Proteins
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