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Journal articles on the topic 'Photomorphogenesi'

Author: Grafiati

Published: 22 February 2023

Last updated: 31 July 2025

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1

Pepper, Alan E., and Joanne Chory. "Extragenic Suppressors of the Arabidopsis det1 Mutant Identify Elements of Flowering-Time and Light-Response Regulatory Pathways." Genetics 145, no. 4 (1997): 1125–37. http://dx.doi.org/10.1093/genetics/145.4.1125.

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Light regulation of seedling morphogenesis is mediated by photoreceptors that perceive red, far-red, blue and UV light. Photomorphogenetic mutants of Arabidopsis have identified several of the primary photoreceptors, as well as a set of negative regulators of seedling photomorphogenesis, including DET1, that appear to act downstream of the photoreceptors. To study the regulatory context in which DET1 acts to repress photomorphogenesis, we used a simple morphological screen to isolate extragenic mutations in six loci, designated ted (for reversal of the det phenotype), that partially or fully s

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2

Zhmurko, V. V., O. O. Avksentieva, and Y. D. Batuieva. "Photomorphogenesis and content of carbohydrates in the axial organs of field pean seedlings under the influence of selective light." 47, no. 47 (September 23, 2022): 27–39. http://dx.doi.org/10.26565/2075-3810-2022-47-03.

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Background: Light is a multifaceted exogenous factor that plays an important role in plant growth and development. The spectral composition of light is determinative for the regulation of photomorphogenetic processes in plants. Nowadays plants have several groups of photoreceptors that include receptors of red (RL) and far red light (FRL) — phytochromes; receptors of UV-A, blue (BL) and green (GL) light — cryptochromes, phototropins, proteins of the ZEITLUPE family, as well as the UV-B receptor — UVR8 protein. One of the possible mechanisms that realize an activation of photoreceptor systems i

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3

Blacquière, T. "PHOTOMORPHOGENESIS." Acta Horticulturae, no. 305 (April 1992): 113–15. http://dx.doi.org/10.17660/actahortic.1992.305.17.

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4

Nemhauser, Jennifer, and Joanne Chory. "Photomorphogenesis." Arabidopsis Book 1 (January 2002): e0054. http://dx.doi.org/10.1199/tab.0054.

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5

Arsovski, Andrej A., Anahit Galstyan, Jessica M. Guseman, and Jennifer L. Nemhauser. "Photomorphogenesis." Arabidopsis Book 10 (January 2012): e0147. http://dx.doi.org/10.1199/tab.0147.

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6

Yang, Chuanwei, Liufan Yin, Famin Xie, et al. "AtINO80 represses photomorphogenesis by modulating nucleosome density and H2A.Z incorporation in light-related genes." Proceedings of the National Academy of Sciences 117, no. 52 (2020): 33679–88. http://dx.doi.org/10.1073/pnas.2001976117.

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Photomorphogenesis is a critical developmental process bridging light-regulated transcriptional reprogramming with morphological changes in organisms. Strikingly, the chromatin-based transcriptional control of photomorphogenesis remains poorly understood. Here, we show that the Arabidopsis (Arabidopsis thaliana) ortholog of ATP-dependent chromatin-remodeling factor AtINO80 represses plant photomorphogenesis. Loss of AtINO80 inhibited hypocotyl cell elongation and caused anthocyanin accumulation. Both light-induced genes and dark-induced genes were affected in the atino80 mutant. Genome-wide oc

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7

Pollock, Robert, Margaret J. McMahon, and John W. Kelly. "COMMUNICATING IN PHOTOMORPHOGENESIS." HortScience 26, no. 5 (1991): 485e—485. http://dx.doi.org/10.21273/hortsci.26.5.485e.

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Description of the light environment used in photomorphogenic research varies greatly among research teams. The environment is often described as the ratio of red (R) to far-red (FR) light, particulary when involvement of the phytochrome system is suspected. There is disagreement in the appropriate center and range of values for each ratio component. Often the center for R is reported as 660 nm. However, in chlorophyll-containing tissue 645 nm may be more appropriate because of the absorption of chlorophyll at 660. Band widths around a selected peak also vary. The widths generally are 10 or 10

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8

Maas, F. M. "PHOTOMORPHOGENESIS IN ROSES." Acta Horticulturae, no. 305 (April 1992): 109–10. http://dx.doi.org/10.17660/actahortic.1992.305.15.

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9

Grace, J., H. Smith, and M. G. Holmes. "Techniques in Photomorphogenesis." Journal of Ecology 74, no. 1 (1986): 312. http://dx.doi.org/10.2307/2260380.

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10

Jones, H. G., R. E. Kendrick, and G. H. M. Kronenberg. "Photomorphogenesis in Plants." Journal of Ecology 76, no. 1 (1988): 293. http://dx.doi.org/10.2307/2260473.

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11

Vanderwoude, William J., and Steven J. Britz. "PHOTOMORPHOGENESIS IN PLANTS." Photochemistry and Photobiology 56, no. 5 (1992): VII—VIII. http://dx.doi.org/10.1111/j.1751-1097.1992.tb02203.x.

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12

Altamura, M. M., M. Tomassi, B. Borkowska, et al. "Session 04 Photomorphogenesis." Biologia plantarum 36, Suppl.1 (1994): S59—S65. http://dx.doi.org/10.1007/bf02931116.

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13

Kendrick, Richard E. "PHOTOMORPHOGENESIS IN PLANTS." Photochemistry and Photobiology 52, no. 1 (1990): 1. http://dx.doi.org/10.1111/j.1751-1097.1990.tb01746.x.

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14

KRAEPIEL, Y., and E. MIGINIAC. "Photomorphogenesis and phytohormones." Plant, Cell and Environment 20, no. 6 (1997): 807–12. http://dx.doi.org/10.1046/j.1365-3040.1997.d01-111.x.

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15

Jennings, RobertC. "Photomorphogenesis in plants." Journal of Photochemistry and Photobiology B: Biology 2, no. 4 (1988): 533–34. http://dx.doi.org/10.1016/1011-1344(88)85082-6.

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16

Ruyters, Günter. "Photomorphogenese bei Algen." Biologie in unserer Zeit 18, no. 2 (1988): 40–46. http://dx.doi.org/10.1002/biuz.19880180203.

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17

Huang, Yuewei, Hui Xiong, Yuxin Xie, et al. "BBX24 Interacts with DELLA to Regulate UV-B-Induced Photomorphogenesis in Arabidopsis thaliana." International Journal of Molecular Sciences 23, no. 13 (2022): 7386. http://dx.doi.org/10.3390/ijms23137386.

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UV-B radiation, sensed by the photoreceptor UVR8, induces signal transduction for plant photomorphogenesis. UV-B radiation affects the concentration of the endogenous plant hormone gibberellin (GA), which in turn triggers DELLA protein degradation through the 26S proteasome pathway. DELLA is a negative regulator in GA signaling, partially relieving the inhibition of hypocotyl growth induced by UV-B in Arabidopsis thaliana. However, GAs do usually not work independently but integrate in complex networks linking to other plant hormones and responses to external environmental signals. Until now,

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18

Ren, Hui, Jiupan Han, Panyu Yang, et al. "Two E3 ligases antagonistically regulate the UV-B response inArabidopsis." Proceedings of the National Academy of Sciences 116, no. 10 (2019): 4722–31. http://dx.doi.org/10.1073/pnas.1816268116.

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Photomorphogenesis is a pivotal developmental strategy used by plants to respond to environmental light levels. During emergence from the soil and the establishment of photomorphogenesis, seedlings encounter increasing levels of UV-B irradiation and develop adaptive responses accordingly. However, the molecular mechanisms that orchestrate UV-B signaling cascades remain elusive. Here, we provide biochemical and genetic evidence that the prolonged signaling circuits of UV-B–induced photomorphogenesis involve two sets of E3 ligases and a transcription factor inArabidopsis thaliana. The UV-B–induc

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19

Salmena, Leonardo, and Razqallah Hakem. "From photomorphogenesis to cancer." Cell Cycle 12, no. 2 (2013): 205–6. http://dx.doi.org/10.4161/cc.23422.

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20

Haupt, Wolfgang. "SIGNAL TRANSDUCTION IN PHOTOMORPHOGENESIS." Photochemistry and Photobiology 52, no. 1 (1990): 261–63. http://dx.doi.org/10.1111/j.1751-1097.1990.tb01783.x.

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21

Schaffner, Kurt. "Molecular aspects of photomorphogenesis." Journal of Photochemistry and Photobiology B: Biology 4, no. 1 (1989): 135. http://dx.doi.org/10.1016/1011-1344(89)80116-2.

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22

Krawczyszyn, Józef, and Teresa Krawczyszyn. "Photomorphogenesis in Dracaena draco." Trees 30, no. 3 (2015): 647–64. http://dx.doi.org/10.1007/s00468-015-1307-z.

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23

Lin, Fang, Jing Cao, Jiale Yuan, Yuxia Liang, and Jia Li. "Integration of Light and Brassinosteroid Signaling during Seedling Establishment." International Journal of Molecular Sciences 22, no. 23 (2021): 12971. http://dx.doi.org/10.3390/ijms222312971.

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Light and brassinosteroid (BR) are external stimuli and internal cue respectively, that both play critical roles in a wide range of developmental and physiological process. Seedlings grown in the light exhibit photomorphogenesis, while BR promotes seedling etiolation. Light and BR oppositely control the development switch from skotomorphogenesis in the dark to photomorphogenesis in the light. Recent progress report that substantial components have been identified as hubs to integrate light and BR signals. Photomorphogenic repressors including COP1, PIFs, and AGB1 have been reported to elevate

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24

Hamasaki, Hidefumi, Madoka Ayano, Ayako Nakamura, et al. "Light Activates Brassinosteroid Biosynthesis to Promote Hook Opening and Petiole Development in Arabidopsis thaliana." Plant and Cell Physiology 61, no. 7 (2020): 1239–51. http://dx.doi.org/10.1093/pcp/pcaa053.

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Abstract Although brassinosteroids (BRs) have been proposed to be negative regulators of photomorphogenesis, their physiological role therein has remained elusive. We studied light-induced photomorphogenic development in the presence of the BR biosynthesis inhibitor, brassinazole (Brz). Hook opening was inhibited in the presence of Brz; this inhibition was reversed in the presence of brassinolide (BL). Hook opening was accompanied by cell expansion on the inner (concave) side of the hook. This cell expansion was inhibited in the presence of Brz but was restored upon the addition of BL. We then

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25

Keiller, D. R. "Book review: Photomorphogenesis in Plants." Outlook on Agriculture 16, no. 4 (1987): 205. http://dx.doi.org/10.1177/003072708701600423.

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26

Alabadí, David, Joan Gil, Miguel A. Blázquez, and José L. García-Martínez. "Gibberellins Repress Photomorphogenesis in Darkness." Plant Physiology 134, no. 3 (2004): 1050–57. http://dx.doi.org/10.1104/pp.103.035451.

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27

Wada, M., and A. Kadota. "Photomorphogenesis in Lower Green Plants." Annual Review of Plant Physiology and Plant Molecular Biology 40, no. 1 (1989): 169–91. http://dx.doi.org/10.1146/annurev.pp.40.060189.001125.

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28

Whitelam, Garry C., and Karen J. Halliday. "Photomorphogenesis: Phytochrome takes a partner!" Current Biology 9, no. 6 (1999): R225—R227. http://dx.doi.org/10.1016/s0960-9822(99)80135-3.

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29

Boccalandro, Hern�n E., Mar�a C. Rossi, Yusuke Saijo, Xing-Wang Deng, and Jorge J. Casal. "Promotion of photomorphogenesis by COP1." Plant Molecular Biology 56, no. 6 (2004): 905–15. http://dx.doi.org/10.1007/s11103-004-5919-8.

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30

Achard, Patrick, Lili Liao, Caifu Jiang, et al. "DELLAs Contribute to Plant Photomorphogenesis." Plant Physiology 143, no. 3 (2007): 1163–72. http://dx.doi.org/10.1104/pp.106.092254.

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31

Han, Yun-Jeong, Pill-Soon Song, and Jeong-ll Kim. "Phytochrome-mediated photomorphogenesis in plants." Journal of Plant Biology 50, no. 3 (2007): 230–40. http://dx.doi.org/10.1007/bf03030650.

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32

Whitelam, Garry C., Samita Patel, and Paul F. Devlin. "Phytochromes and photomorphogenesis in Arabidopsis." Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences 353, no. 1374 (1998): 1445–53. http://dx.doi.org/10.1098/rstb.1998.0300.

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Plants have evolved exquisite sensory systems for monitoring their light environment. The intensity, quality, direction and duration of light are continuously monitored by the plant and the information gained is used to modulate all aspects of plant development. Several classes of distinct photoreceptors, sensitive to different regions of the light spectrum, mediate the developmental responses of plants to light signals. The red–far–red light–absorbing, reversibly photochromic phytochromes are perhaps the best characterized of these. Higher plants possess a family of phytochromes, the apoprote

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33

Pepper, Alan, Terrence P. Delaney, and Joanne Chory. "Genetic interactions in plant photomorphogenesis." Seminars in Developmental Biology 4, no. 1 (1993): 15–22. http://dx.doi.org/10.1006/sedb.1993.1003.

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34

Xu, Peng, Huiru Chen, Ting Li, et al. "Blue light-dependent interactions of CRY1 with GID1 and DELLA proteins regulate gibberellin signaling and photomorphogenesis in Arabidopsis." Plant Cell 33, no. 7 (2021): 2375–94. http://dx.doi.org/10.1093/plcell/koab124.

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Abstract Cryptochromes are blue light photoreceptors that mediate various light responses in plants and mammals. In Arabidopsis (Arabidopsis thaliana), cryptochrome 1 (CRY1) mediates blue light-induced photomorphogenesis, which is characterized by reduced hypocotyl elongation and enhanced anthocyanin production, whereas gibberellin (GA) signaling mediated by the GA receptor GA-INSENSITIVE DWARF1 (GID1) and DELLA proteins promotes hypocotyl elongation and inhibits anthocyanin accumulation. Whether CRY1 control of photomorphogenesis involves regulation of GA signaling is largely unknown. Here, w

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35

Yu, Xiaodan, Jie Dong, Zhaoguo Deng, et al. "Arabidopsis PP6 phosphatases dephosphorylate PIF proteins to repress photomorphogenesis." Proceedings of the National Academy of Sciences 116, no. 40 (2019): 20218–25. http://dx.doi.org/10.1073/pnas.1907540116.

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The PHYTOCHROME-INTERACTING FACTORs (PIFs) play a central role in repressing photomorphogenesis, and phosphorylation mediates the stability of PIF proteins. Although the kinases responsible for PIF phosphorylation have been extensively studied, the phosphatases that dephosphorylate PIFs remain largely unknown. Here, we report that seedlings with mutations in FyPP1 and FyPP3, 2 genes encoding the catalytic subunits of protein phosphatase 6 (PP6), exhibited short hypocotyls and opened cotyledons in the dark, which resembled the photomorphogenic development of dark-grown pifq mutants. The hypocot

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36

Kim, Byung Chul, Daniel J. Tennessen, and Robert L Last. "UV-B-induced photomorphogenesis inArabidopsis thaliana." Plant Journal 15, no. 5 (1998): 667–74. http://dx.doi.org/10.1046/j.1365-313x.1998.00246.x.

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37

Liu, Hongtao, Rongcheng Lin, and Xing Wang Deng. "Photobiology: Light signal transduction and photomorphogenesis." Journal of Integrative Plant Biology 62, no. 9 (2020): 1267–69. http://dx.doi.org/10.1111/jipb.13004.

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38

Fankhauser, Christian, and Joanne Chory. "Photomorphogenesis: Light receptor kinases in plants!" Current Biology 9, no. 4 (1999): R123—R126. http://dx.doi.org/10.1016/s0960-9822(99)80078-5.

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39

Corrochano, Luis M., and Enrique Cerd�-Olmedo. "Photomorphogenesis inPhycomyces: Dependence on environmental conditions." Planta 174, no. 3 (1988): 309–14. http://dx.doi.org/10.1007/bf00959515.

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40

Li, Jigang, Li Yang, Dan Jin, Cynthia D. Nezames, William Terzaghi, and Xing Wang Deng. "UV-B-induced photomorphogenesis in Arabidopsis." Protein & Cell 4, no. 7 (2013): 485–92. http://dx.doi.org/10.1007/s13238-013-3036-7.

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41

Jang, Geng-Jen, Jun-Yi Yang, Hsu-Liang Hsieh, and Shu-Hsing Wu. "Processing bodies control the selective translation for optimal development of Arabidopsis young seedlings." Proceedings of the National Academy of Sciences 116, no. 13 (2019): 6451–56. http://dx.doi.org/10.1073/pnas.1900084116.

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Germinated plant seeds buried in soil undergo skotomorphogenic development before emergence to reach the light environment. Young seedlings transitioning from dark to light undergo photomorphogenic development. During photomorphogenesis, light alters the transcriptome and enhances the translation of thousands of mRNAs during the dark-to-light transition inArabidopsisyoung seedlings. About 1,500 of these mRNAs have comparable abundance before and after light treatment, which implies widespread translational repression in dark-grown seedlings. Processing bodies (p-bodies), the cytoplasmic granul

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42

Voronkova, Tatiana, Vera Kondratieva, Lyudmila Olehnovich, Liliya Ahmetova, and Olga Molkanova. "The effect of the spectral composition of light on some leaves biochemical and morphological parameters of Hydrangea macrophylla (Thunb.) Ser. regenerants under in vitro conditions." АгроЭкоИнфо 5, no. 53 (2022): 33. http://dx.doi.org/10.51419/202125533.

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Hydrangea macrophylla (Thunb.) Ser. is one of the most popular ornamental crops used in landscaping. The growing area of H. macrophylla is expanding due to climate warming. Light plays an important role in plant ontogenesis, determining photosynthetic pigments and photomorphogenesis. n the photomorphogenesis of plants, an important role is assigned to the light of the red and blue bands of the spectrum. In the photomorphogenesis of plants, the light of the red and blue bands of the spectrum plays the greatest role. In our studies, a combination of red (70%) and blue (30%) spectra was used in t

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43

Adamse, Paulien, Richard E. Kendrick, and Maarten Koornneef. "PHOTOMORPHOGENETIC MUTANTS OF HIGHER PLANTS." Photochemistry and Photobiology 48, no. 6 (1988): 833–41. http://dx.doi.org/10.1111/j.1751-1097.1988.tb02898.x.

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44

Zhao, Xianhai, Yan Jiang, Jian Li, et al. "COP1 SUPPRESSOR 4 promotes seedling photomorphogenesis by repressingCCA1andPIF4expression inArabidopsis." Proceedings of the National Academy of Sciences 115, no. 45 (2018): 11631–36. http://dx.doi.org/10.1073/pnas.1813171115.

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CONSTITUTIVELY PHOTOMORPHOGENIC 1 (COP1) and DE-ETIOLATED 1 (DET1) are founding components of two central repressor complexes of photomorphogenesis that trigger the degradation of a larger number of photomorphogenic-promoting factors in darkness. Here, we identify COP1 SUPPRESSOR 4 (CSU4) as a genetic suppressor of thecop1-6mutation. Mutations inCSU4largely rescued the constitutively photomorphogenic phenotype ofcop1-6anddet1-1in darkness. Loss of CSU4 function resulted in significantly longer hypocotyl in the light. Further biochemical studies revealed that CSU4 physically interacts with CIRC

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45

Eckardt, Nancy A. "From Darkness into Light: Factors Controlling Photomorphogenesis." Plant Cell 13, no. 2 (2001): 219. http://dx.doi.org/10.2307/3871271.

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46

Decoteau, Dennis R., Heather A. Hatt, John W. Kelly, et al. "Applications of Photomorphogenesis Research to Horticultural Systems." HortScience 28, no. 10 (1993): 974–1063. http://dx.doi.org/10.21273/hortsci.28.10.974.

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47

He, Zhimin, Xiaoying Zhao, Fanna Kong, Zecheng Zuo, and Xuanming Liu. "TCP2 positively regulatesHY5/HYHand photomorphogenesis in Arabidopsis." Journal of Experimental Botany 67, no. 3 (2015): 775–85. http://dx.doi.org/10.1093/jxb/erv495.

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48

Corrochano, Luis M., and Enrique Cerda -Olmedo. "PHOTOMORPHOGENESIS IN Phycomyces and IN OTHER FUNGI." Photochemistry and Photobiology 54, no. 2 (1991): 319–27. http://dx.doi.org/10.1111/j.1751-1097.1991.tb02023.x.

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49

Flores, Rafael, Enrique Cerdá-Olmedo, and Luis M. Corrochano. "Separate Sensory Pathways for Photomorphogenesis in Phycomyces." Photochemistry and Photobiology 67, no. 4 (1998): 467–72. http://dx.doi.org/10.1111/j.1751-1097.1998.tb05229.x.

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50

Parks, Brian M. "The Red Side of Photomorphogenesis: Figure 1." Plant Physiology 133, no. 4 (2003): 1437–44. http://dx.doi.org/10.1104/pp.103.029702.

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