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Photoreceptor Signaling Networks in Plant Responses to Shade
Open accessAbstract
The dynamic light environment of vegetation canopies is perceived by phytochromes, cryptochromes, phototropins, and UV RESISTANCE LOCUS 8 (UVR8). These receptors control avoidance responses to preclude exposure to limiting or excessive light and acclimation responses to cope with conditions that cannot be avoided. The low red/far-red ratios of shade light reduce phytochrome B activity, which allows PHYTOCHROME INTERACTING FACTORS (PIFs) to directly activate the transcription of auxin-synthesis genes, leading to shade-avoidance responses. Direct PIF interaction with DELLA proteins links gibberellin and brassinosteroid signaling to shade avoidance. Shade avoidance also requires CONSTITUTIVE PHOTOMORPHOGENESIS 1 (COP1), a target of cryptochromes, phytochromes, and UVR8. Multiple regulatory loops and the input of the circadian clock create a complex network able to respond even to subtle threats of competition with neighbors while still compensating for major environmental fluctuations such as the day-night cycles.
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“Plants quantify this ratio through the phytochrome system and react with the shade avoidance syndrome that enables plants to outgrow the competitors for light (Casal, 2013; Pierik and de Wit, 2014).”
From Shaping plant architecture (2015) · cites this paper as Casal, 2013
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“Arabidopsis thaliana homeobox 2 (ATHB2) and ATHB4, HD-Zip II proteins, are induced by a low ratio of red to far-red light and contribute to the shade avoidance response, including hypocotyl elongation [15,16].”
BackgroundEffects of nitrogen fertilization and planting density on intermediate wheatgrass yield
Fernandez, C. W., Ehlke, N. J., Sheaffer, C. C., & Jungers, J. M. (2020) · Agronomy Journal · doi:10.1002/agj2.20351 · Cited by 41
Rockwell, N. C., Martin, S. S., Lim, S., Lagarias, J. C., & Ames, J. B. (2015) · Biochemistry · doi:10.1021/acs.biochem.5b00438 · Cited by 41
Transmissivity of solar radiation within a Picea sitchensis stand under various sky conditions
Dengel, S., Grace, J., & MacArthur, A. (2015) · Biogeosciences · doi:10.5194/bg-12-4195-2015 · Cited by 40
“Blue light may have important implications for stomatal control, causing stomatal opening (Morison and Jarvis, 1983), while the red : far-red ratio is known to influence photomorphogenesis, heating regulation, as well as stem elongation and chlorophyll synthesis (Gates, 1965; Smith, 1982; Wherley et al., 2005; Casal,…”
BackgroundTan, P. Y., & Ismail, M. R. B. (2014) · Urban forestry & urban greening · doi:10.1016/j.ufug.2014.05.011 · Cited by 40
SPA proteins: SPAnning the gap between visible light and gene expression
Menon, C., Sheerin, D. J., & Hiltbrunner, A. (2016) · Planta · doi:10.1007/s00425-016-2509-3 · Cited by 41
Phytochrome A Protects Tomato Plants From Injuries Induced by Continuous Light
Vélez‐Ramírez, A. I., Vreugdenhil, D., Millenaar, F. F., & van Ieperen, W. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.00019 · Cited by 43
“Evidence shows that, similar to other phytochromes, PHYA Pfr is the active form in signaling, yet photocycling between Pr and Pfr forms is needed to both bind and, once inside the nucleus, release the FHY1/FHL transporters (Rausenberger et al., 2011).”
BackgroundInfluentialSun, J., Lu, J., Bai, M., Chen, Y., Wang, W., Fan, C., Liu, J., Ning, G., & Wang, C. (2021) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiab109 · Cited by 40
Dreccer, M. F., Zwart, A., Schmidt, R., Condon, A. G., Awasi, M. A., Grant, T. J., Gallé, A., Bourot, S., & Frohberg, C. (2022) · Plant Cell & Environment · doi:10.1111/pce.14390 · Cited by 39
Organ-specific COP1 control of BES1 stability adjusts plant growth patterns under shade or warmth
Rojas, C. C., Bianchimano, L., Oh, J., Romero‐Montepaone, S., Tarkowská, D., Minguet, E. G., Schön, J., Hourquet, M. G., Flugel, T., Blázquez, M. A., et al. (2022) · Developmental Cell · doi:10.1016/j.devcel.2022.07.003 · Cited by 39
Self-citationNi, J., Liao, Y., Zhang, M., Chen, P., Yang, Q., Bai, S., & Teng, Y. (2022) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.2c07137 · Cited by 39
Mathematical Models Light Up Plant Signaling
Chew, Y. H., Smith, R. W., Jones, H. J., Seaton, D. D., Grima, R., & Halliday, K. (2014) · The Plant Cell · doi:10.1105/tpc.113.120006 · Cited by 38
“Casal, J.J. (2013). Photoreceptor signaling networks in plant responses to”
BackgroundA judgment and decision‐making model for plant behavior
Karban, R., & Orrock, J. L. (2018) · Ecology · doi:10.1002/ecy.2418 · Cited by 39
The karrikin ‘calisthenics’: Can compounds derived from smoke help in stress tolerance?
Banerjee, A., Tripathi, D. K., & Roychoudhury, A. (2018) · Physiologia Plantarum · doi:10.1111/ppl.12836 · Cited by 43
Cell wall structure and composition is affected by light quality in tomato seedlings
Falcioni, R., Moriwaki, T., Pérez-Llorca, M., Munné‐Bosch, S., Gibin, M. S., Sato, F., Pelozo, A., Pattaro, M. C., Giacomelli, M. E., Rüggeberg, M., et al. (2019) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2019.111745 · Cited by 39
Artificial selection for grain yield has increased net CO2 exchange of the ear leaf in maize crops
Cagnola, J. I., Parco, M., Rotili, D. H., Ploschuk, E. L., Curín, F., Amas, J. I., Luque, S. F., Maddonni, G. Á., Otegui, M. E., & Casal, J. J. (2021) · Journal of Experimental Botany · doi:10.1093/jxb/erab119 · Cited by 41
Self-citationThere and Back Again: Loss and Reacquisition of Two‐Cys Photocycles in Cyanobacteriochromes
Rockwell, N. C., Martin, S. S., & Lagarias, J. C. (2017) · Photochemistry and Photobiology · doi:10.1111/php.12708 · Cited by 39
“For example, land plants utilize phytochrome proteins to detect red and far-red light (2-6).”
Phytochrome B links the environment to transcription
Hernando, C. E., Murcia, M. G., Pereyra, M. E., Sellaro, R., & Casal, J. J. (2021) · Journal of Experimental Botany · doi:10.1093/jxb/erab037 · Cited by 38
Self-citationEmerging Hubs in Plant Light and Temperature Signaling
Lorenzo, C. D., Sánchez‐Lamas, M., Antonietti, M. S., & Cerdán, P. D. (2015) · Photochemistry and Photobiology · doi:10.1111/php.12535 · Cited by 40
Vélez‐Ramírez, A. I., Dünner-Planella, G., Vreugdenhil, D., Millenaar, F. F., & van Ieperen, W. (2017) · Functional Plant Biology · doi:10.1071/fp16285 · Cited by 38
Shade avoidance responses become more aggressive in warm environments
Romero‐Montepaone, S., Poodts, S., Fischbach, P., Sellaro, R., Zurbriggen, M. D., & Casal, J. J. (2020) · Plant Cell & Environment · doi:10.1111/pce.13720 · Cited by 38
Self-citationPhytochrome B dynamics departs from photoequilibrium in the field
Sellaro, R., Smith, R. W., Legris, M., Fleck, C. C., & Casal, J. J. (2018) · Plant Cell & Environment · doi:10.1111/pce.13445 · Cited by 38
Self-citationGhose, A. K., Abdullah, S. N. A., Hatta, M. A. M., & Wahab, P. E. M. (2022) · Agronomy · doi:10.3390/agronomy12081957 · Cited by 37
“The freshly added auxin in the growth media consequently carried to the bases of the lamina, petiole, and hypocotyl, where it promotes cell elongation in the petiole and hypocotyl [70–73].”
Molecular interaction of jasmonate and phytochrome A signalling
Hsieh, H.-L., & Okamoto, H. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/eru230 · Cited by 37
Shade avoidance syndrome in soybean and ideotype toward shade tolerance
Lyu, X., Mu, R., & Liu, B. (2023) · Molecular Breeding · doi:10.1007/s11032-023-01375-3 · Cited by 36
“Plants possess several photoreceptors that are sensitive to changes in the spectral composition of light (Casal 2013; Paik and Huq 2019).”
BackgroundLee, I., Kim, K., Lee, S., Lee, S., Hwang, E., Shin, K., Kim, D., Choi, J., Choi, H., Cha, J. S., et al. (2018) · Journal of Experimental Botany · doi:10.1093/jxb/ery164 · Cited by 36
Far-red light during cultivation induces postharvest cold tolerance in tomato fruit
Affandi, F. Y., Verdonk, J. C., Ouzounis, T., Ji, Y., Woltering, E. J., & Schouten, R. E. (2019) · Postharvest Biology and Technology · doi:10.1016/j.postharvbio.2019.111019 · Cited by 36
Evolutionary origin of phytochrome responses and signaling in land plants
Inoue, K., Nishihama, R., & Kohchi, T. (2017) · Plant Cell & Environment · doi:10.1111/pce.12908 · Cited by 36
Metadata
- Authors
- Casal, J. J.
- Affiliations
- Consejo Nacional de Investigaciones Científicas y Técnicas (AR)
- Corresponding author
- Casal, Jorge J.
- ORCID
- Casal, Jorge J.
- Venue
- Annual Review of Plant Biology
- Publisher
- Annual Reviews
- Published
- 2013-04-29
- Volume
- 64
- Issue
- 1
- Pages
- 403-427
- ISSN
- 1543-5008 (ISSN-L)
- 1545-2123
- OpenAlex
- W2107201571
- Cited by
- 865
- References
- 144
- Citations by year
- 2026: 81 · 2025: 66 · 2024: 72 · 2023: 61 · 2022: 79 · 2021: 91 · 2020: 67 · 2019: 60 · 2018: 62 · 2017: 60 · 2016: 58 · 2015: 44 · 2014: 51 · 2013: 13
- FWCI
- 5.94
- Type
- journal article
- Language
- en
- Open access
- green
- hdl.handle.net
- Licence
- cc-by-nc-nd
- Locations
- Annual Review of Plant Biology (publishedVersion)
- PubMed (publishedVersion)
- CONICET Digital (CONICET) (submittedVersion, cc-by-nc-nd)
- Funders
- Consejo Nacional de Investigaciones Científicas y Técnicas
- Universidad de Buenos Aires (CONICET)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Light effects on plants
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Parasitism and Resistance
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Molecular Biology Research
- Keywords
- shade avoidance, photoreceptors, phytochrome, cryptochrome, phototropin, UVR8, phytochrome-interacting factors, DELLA proteins, gibberellin signaling, brassinosteroid signaling, auxin biosynthesis, COP1, circadian clock, red:far-red ratio, plant light signaling, canopy light environment
- MeSH terms
- Gibberellins, Light, Phytochrome, Plant Growth Regulators, Plants, Signal Transduction, Ecosystem, Photoreceptors, Plant
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