Baranova, M. Systematic anatomy of the leaf epidermis in the Magnoliaceae and some related families. Int. Assoc. Plant Taxon. (IAPT) 21, 447–469 (1972).
Suzuki, S., Kiyoshi, I., Saneyoshi, U., Yoshihiko, T. & Nobuhiro, T. Population differentiation and gene flow within ametapopulation of a threatened tree, Magnolia stellata (magnoliaceae). Am. J. Bot. 94, 128–136 (2007).
Google Scholar
Tan, M. et al. Study on seed germination and seedling growth of Magnolia officinalis in different habitats. J. Ecol. Rural Environ. 34, 910–916 (2018).
Zezhi, Y. et al. Study on population distribution and community structure of Magnolia sinostellata. Zhejiang For. Sci. Technol. 35, 47–52 (2015).
Yu, Q. et al. Light deficiency and waterlogging affect chlorophyll metabolism and photosynthesis in Magnolia sinostellata. Trees 33, 11–22. https://doi.org/10.1007/s00468-018-1753-5 (2018).
Google Scholar
Promis, A. & Allen, R. B. Tree seedlings respond to both light and soil nutrients in a Patagonian evergreen-deciduous forest. PLoS ONE 12, e0188686. https://doi.org/10.1371/journal.pone.0188686 (2017).
Google Scholar
Qin, Y. Effect of Light intensity and waterlogging on the physiology characteristic and the relative expression of genes in Magnolia sinostellata. 33, 11–22 (2018).
Chen, T. et al. Shade effects on peanut yield associate with physiological and expressional regulation on photosynthesis and sucrose metabolism. Int. J. Mol. Sci. https://doi.org/10.3390/ijms21155284 (2020).
Google Scholar
Yao, X. et al. Effect of shade on leaf photosynthetic capacity, light-intercepting, electron transfer and energy distribution of soybeans. Plant Growth Regul. 83, 409–416. https://doi.org/10.1007/s10725-017-0307-y (2017).
Google Scholar
Wu, Y., Gong, W. & Yang, W. Shade inhibits leaf size by controlling cell proliferation and enlargement in soybean. Sci. Rep. 7, 9259. https://doi.org/10.1038/s41598-017-10026-5 (2017).
Google Scholar
Zhao, D., Hao, Z. & Tao, J. Effects of shade on plant growth and flower quality in the herbaceous peony (Paeonia lactiflora Pall.). Plant Physiol. Biochem. 61, 187–196. https://doi.org/10.1016/j.plaphy.2012.10.005 (2012).
Google Scholar
Tamaki, I. et al. Evaluation of a field experiment for the conservation of a Magnolia stellata stand using clear-cutting. Landscape Ecol. Eng. 14, 269–276. https://doi.org/10.1007/s11355-018-0348-z (2018).
Google Scholar
Jian, W. et al. Photosynthesis and chlorophyll fluorescence reaction to different shade stresses of weak light sensitive maize. Pak. J. Bot. 49, 1681–1688 (2017).
Quail, P. H. The phytochrome family dissection of functional roles and signalling pathways among family members. Philos. Trans. R. Soc. B 353, 1399–1403 (1998).
Google Scholar
Yang, F. et al. Effect of interactions between light intensity and red-to- far-red ratio on the photosynthesis of soybean leaves under shade condition. Environ. Exp. Bot. 150, 79–87. https://doi.org/10.1016/j.envexpbot.2018.03.008 (2018).
Google Scholar
Luesse, D. R., DeBlasio, S. L. & Hangarter, R. P. Integration of Phot1, Phot2, and PhyB signalling in light-induced chloroplast movements. J. Exp. Bot. 61, 4387–4397. https://doi.org/10.1093/jxb/erq242 (2010).
Google Scholar
Dinakar, C., Vishwakarma, A., Raghavendra, A. S. & Padmasree, K. Alternative oxidase pathway optimizes photosynthesis during osmotic and temperature stress by regulating cellular ROS, malate valve and antioxidative systems. Front. Plant Sci. 7, 68. https://doi.org/10.3389/fpls.2016.00068 (2016).
Google Scholar
Ruban, A. V. Light harvesting control in plants. FEBS Lett. 592, 3030–3039. https://doi.org/10.1002/1873-3468.13111 (2018).
Google Scholar
Wang, J. et al. Photosynthesis and chlorophyll fluorescence reaction to different shade stresses of weak light sensitive maize. Pak. J. Bo. 49, 1681–1688 (2017).
Yamori, W., Shikanai, T. & Makino, A. Photosystem I cyclic electron flow via chloroplast NADH dehydrogenase-like complex performs a physiological role for photosynthesis at low light. Sci. Rep. 5, 13908. https://doi.org/10.1038/srep13908 (2015).
Google Scholar
Ng, J. & Mueller-Cajar, O. Rubisco activase remodels plant Rubisco via the large subunit N-terminus. bioRxiv https://doi.org/10.1101/2020.06.14.151407 (2020).
Google Scholar
Zhang, Y., Liu, N., Wang, W., Sun, J. & Zhu, L. Photosynthesis and related metabolic mechanism of promoted rice (Oryza sativa L.) growth by TiO2 nanoparticles. Front. Environ. Sci. Eng. https://doi.org/10.1007/s11783-020-1282-5 (2020).
Google Scholar
Suzuki, Y. & Makino, A. Translational downregulation of RBCL is operative in the coordinated expression of Rubisco genes in senescent leaves in rice. J. Exp. Bot. 64, 1145–1152. https://doi.org/10.1093/jxb/ers398 (2013).
Google Scholar
Sun, J. et al. Low light stress down-regulated rubisco gene expression and photosynthetic capacity during cucumber (Cucumis sativus L.) leaf development. J. Integr. Agric. 13, 997–1007. https://doi.org/10.1016/s2095-3119(13)60670-x (2014).
Google Scholar
Wu, H. Y., Liu, L. A., Shi, L., Zhang, W. F. & Jiang, C. D. Photosynthetic acclimation during low-light-induced leaf senescence in post-anthesis maize plants. Photosynth. Res. 150, 313–326. https://doi.org/10.1007/s11120-021-00851-1 (2021).
Google Scholar
Zou, D., Gao, K. & Chen, W. Photosynthetic carbon acquisition in Sargassum henslowianum (Fucales, Phaeophyta), with special reference to the comparison between the vegetative and reproductive tissues. Photosynth. Res. 107, 159–168. https://doi.org/10.1007/s11120-010-9612-2 (2011).
Google Scholar
Wu, Z.-F. et al. Effects of low light stress on rubisco activity and the ultrastructure of chloroplast in functional leaves of peanut. Chin. J. Plant Ecol. 38, 740–748. https://doi.org/10.3724/SP.J.1258.2014.00069 (2014).
Google Scholar
Valladares, F. et al. The greater seedling high-light tolerance of Quercus robur over Fagus sylvatica is linked to a greater physiological plasticity. Trees 16, 395–403. https://doi.org/10.1007/s00468-002-0184-4 (2002).
Google Scholar
Rojas-Gonzalez, J. A. et al. Disruption of both chloroplastic and cytosolic FBPase genes results in a dwarf phenotype and important starch and metabolite changes in Arabidopsis thaliana. J. Exp. Bot. 66, 2673–2689. https://doi.org/10.1093/jxb/erv062 (2015).
Google Scholar
Lowe, H., Hobmeier, K., Moos, M., Kremling, A. & Pfluger-Grau, K. Photoautotrophic production of polyhydroxyalkanoates in a synthetic mixed culture of Synechococcus elongatus cscB and Pseudomonas putida cscAB. Biotechnol. Biofuels 10, 190. https://doi.org/10.1186/s13068-017-0875-0 (2017).
Google Scholar
Wang, B. et al. Photosynthesis, sucrose metabolism, and starch accumulation in two NILs of winter wheat. Photosynth. Res. 126, 363–373. https://doi.org/10.1007/s11120-015-0126-9 (2015).
Google Scholar
Myers, J. A. & Kitajima, K. Carbohydrate storage enhances seedling shade and stress tolerance in a neotropical forest. J. Ecol. 95, 383–395. https://doi.org/10.1111/j.1365-2745.2006.01207.x (2007).
Google Scholar
Lestari, D. P. & Nichols, J. D. Seedlings of subtropical rainforest species from similar successional guild show different photosynthetic and morphological responses to varying light levels. Tree Physiol. 37, 186–198. https://doi.org/10.1093/treephys/tpw088 (2017).
Google Scholar
Wu, M., Li, Z. & Wang, J. Transcriptional analyses reveal the molecular mechanism governing shade tolerance in the invasive plant Solidago canadensis. Ecol. Evol. 10, 4391–4406. https://doi.org/10.1002/ece3.6206 (2020).
Google Scholar
Miao, Z. Q. et al. HOMEOBOX PROTEIN52 mediates the crosstalk between ethylene and auxin signaling during primary root elongation by modulating auxin transport-related gene expression. Plant Cell 30, 2761–2778. https://doi.org/10.1105/tpc.18.00584 (2018).
Google Scholar
Liu, B. et al. A domestication-associated gene, CsLH, encodes a phytochrome B protein that regulates hypocotyl elongation in cucumber. Mol. Hortic. https://doi.org/10.1186/s43897-021-00005-w (2021).
Google Scholar
Sun, W. et al. Mediator subunit MED25 physically interacts with phytochrome interacting factor4 to regulate shade-induced hypocotyl elongation in tomato. Plant Physiol. 184, 1549–1562. https://doi.org/10.1104/pp.20.00587 (2020).
Google Scholar
Bawa, G. et al. Gibberellins and auxin regulate soybean hypocotyl elongation under low light and high-temperature interaction. Physiol. Plant 170, 345–356. https://doi.org/10.1111/ppl.13158 (2020).
Google Scholar
Potter, T. I., Rood, S. B. & Zanewich, K. P. Light intensity, gibberellin content and the resolution of shoot growth in Brassica. Planta 207, 505–511 (1999).
Google Scholar
Ballare, C. L., Scopel, A. L. & San, R. A. Foraging for light photosensory ecology and agricultural implications. Plant Cell Environ. 20, 820–825 (1997).
Google Scholar
Hope, E., Gracie, A., Carins-Murphy, M. R., Hudson, C. & Baxter, L. Opium poppy capsule growth and alkaloid production is constrained by shade during early floral development. Ann. Appl. Biol. 176, 296–307 (2020).
Google Scholar
Lu, D. et al. Light deficiency inhibits growth by affecting photosynthesis efficiency as well as JA and ethylene signaling in endangered plant Magnolia sinostellata. Plants https://doi.org/10.3390/plants10112261 (2021).
Google Scholar
Lin, W., Guo, X., Pan, X. & Li, Z. Chlorophyll composition, chlorophyll fluorescence, and grain yield change in esl mutant rice. Int. J. Mol. Sci. https://doi.org/10.3390/ijms19102945 (2018).
Google Scholar
Sano, S. et al. Stress responses of shade-treated tea leaves to high light exposure after removal of shading. Plants (Basel) https://doi.org/10.3390/plants9030302 (2020).
Google Scholar
Liu, D. L. et al. Genetic map construction and QTL analysis of leaf-related traits in soybean under monoculture and relay intercropping. Sci. Rep. 9, 2716. https://doi.org/10.1038/s41598-019-39110-8 (2019).
Google Scholar
Sekhar, S. et al. Comparative transcriptome profiling of low light tolerant and sensitive rice varieties induced by low light stress at active tillering stage. Sci. Rep. 9, 5753. https://doi.org/10.1038/s41598-019-42170-5 (2019).
Google Scholar
Wegener, F., Beyschlag, W. & Werner, C. High intraspecific ability to adjust both carbon uptake and allocation under light and nutrient reduction in Halimium halimifolium L. Front. Plant Sci. 6, 609. https://doi.org/10.3389/fpls.2015.00609 (2015).
Google Scholar
Liu, B. et al. A HY5-COL3-COL13 regulatory chain for controlling hypocotyl elongation in Arabidopsis. Plant Cell Environ. 44, 130–142. https://doi.org/10.1111/pce.13899 (2021).
Google Scholar
Cookson, S. J. & Granier, C. A dynamic analysis of the shade-induced plasticity in Arabidopsis thaliana rosette leaf development reveals new components of the shade-adaptative response. Ann. Bot. 97, 443–452. https://doi.org/10.1093/aob/mcj047 (2006).
Google Scholar
Zhong, X. M., Shi, Z. S., Li, F. H. & Huang, H. J. Photosynthesis and chlorophyll fluorescence of infertile and fertile stalks of paired near-isogenic lines in maize (Zea mays L.) under shade conditions. Photosynthetica 52, 597–603. https://doi.org/10.1007/s11099-014-0071-4 (2014).
Google Scholar
Kittiwongwattana, C. Differential effects of synthetic media on long-term growth, starch accumulation and transcription of ADP-glucosepyrophosphorylase subunit genes in Landoltia punctata. Sci. Rep. 9, 15310. https://doi.org/10.1038/s41598-019-51677-w (2019).
Google Scholar
Sagadevan, G. M. et al. Physiological and molecular insights into drought tolerance. Afr. J. Biotechnol. 1, 28–38 (2002).
Google Scholar
Xiaotao, D. et al. Effects of cytokinin on photosynthetic gas exchange, chlorophyll fluorescence parameters, antioxidative system and carbohydrate accumulation in cucumber (Cucumis sativus L.) under low light. Acta Physiologiae Plant. 35, 1427–1438. https://doi.org/10.1007/s11738-012-1182-9 (2012).
Google Scholar
Sofo, A., Dichio, B., Montanaro, G. & Xiloyannis, C. Photosynthetic performance and light response of two olive cultivars under different water and light regimes. Photosynthetica 47, 602–608 (2009).
Google Scholar
Zhou, Y., Zhu, J., Shao, L. & Guo, M. Current advances in acteoside biosynthesis pathway elucidation and biosynthesis. Fitoterapia 142, 104495. https://doi.org/10.1016/j.fitote.2020.104495 (2020).
Google Scholar
Huang, P. et al. Overexpression of L-type lectin-like protein kinase 1 confers pathogen resistance and regulates salinity response in Arabidopsis thaliana. Plant Sci. 203–204, 98–106. https://doi.org/10.1016/j.plantsci.2012.12.019 (2013).
Google Scholar
Vorontsov, I. I. et al. Crystal structure of an apo form of Shigella flexneri ArsH protein with an NADPH-dependent FMN reductase activity. Protein Sci. 16, 2483–2490. https://doi.org/10.1110/ps.073029607 (2007).
Google Scholar
Guo, M. et al. Proteomic and phosphoproteomic analyses of NaCl stress-responsive proteins in Arabidopsis roots. J. Plant Interact. 9, 396–401. https://doi.org/10.1080/17429145.2013.845262 (2013).
Google Scholar
Smith, C. et al. Alterations in the mitochondrial alternative NAD(P)H Dehydrogenase NDB4 lead to changes in mitochondrial electron transport chain composition, plant growth and response to oxidative stress. Plant Cell Physiol. 52, 1222–1237. https://doi.org/10.1093/pcp/pcr073 (2011).
Google Scholar
Johnson, K. L., Jones, B. J., Bacic, A. & Schultz, C. J. The fasciclin-like arabinogalactan proteins of Arabidopsis. A multigene family of putative cell adhesion molecules. Plant Physiol. 133, 1911–1925. https://doi.org/10.1104/pp.103.031237 (2003).
Google Scholar
Merz, D. et al. T-DNA alleles of the receptor kinase THESEUS1 with opposing effects on cell wall integrity signaling. J. Exp. Bot. 68, 4583–4593. https://doi.org/10.1093/jxb/erx263 (2017).
Google Scholar
Figueiredo, J., Silva, M. S. & Figueiredo, A. Subtilisin-like proteases in plant defence: The past, the present and beyond. Mol. Plant Pathol. 19, 1017–1028. https://doi.org/10.1111/mpp.12567 (2018).
Google Scholar
Sintupachee, S., Promden, W., Ngamrojanavanich, N., Sitthithaworn, W. & De-Eknamkul, W. Functional expression of a putative geraniol 8-hydroxylase by reconstitution of bacterially expressed plant CYP76F45 and NADPH-cytochrome P450 reductase CPR I from Croton stellatopilosus Ohba. Phytochemistry 118, 204–215. https://doi.org/10.1016/j.phytochem.2015.08.005 (2015).
Google Scholar
Chen, Y. et al. Enzymatic reaction-related protein degradation and proteinaceous amino acid metabolism during the black tea (Camellia sinensis) manufacturing process. Foods https://doi.org/10.3390/foods9010066 (2020).
Smidansky, E. D. et al. Expression of a modified ADP-glucose pyrophosphorylase large subunit in wheat seeds stimulates photosynthesis and carbon metabolism. Planta 225, 965–976. https://doi.org/10.1007/s00425-006-0400-3 (2007).
Google Scholar
Mathur, S., Jain, L. & Jajoo, A. Photosynthetic efficiency in sun and shade plants. Photosynthetica https://doi.org/10.1007/s11099-018-0767-y (2018).
Google Scholar
Huang, W., Zhang, S. B. & Liu, T. Moderate photoinhibition of photosystem II significantly affects linear electron flow in the shade-demanding plant panax notoginseng. Front. Plant Sci. 9, 637. https://doi.org/10.3389/fpls.2018.00637 (2018).
Google Scholar
Li, Q. et al. Quantitative trait locus (QTLs) mapping for quality traits of wheat based on high density genetic map combined with bulked segregant analysis RNA-seq (BSR-Seq) indicates that the basic 7S globulin gene is related to falling number. Front. Plant Sci. 11, 600788. https://doi.org/10.3389/fpls.2020.600788 (2020).
Google Scholar
Hashempour, A., Ghasemnezhad, M., Sohani, M. M., Ghazvini, R. F. & Abedi, A. Effects of freezing stress on the expression of fatty acid desaturase (FAD2, FAD6 and FAD7) and beta-glucosidase (BGLC) genes in tolerant and sensitive olive cultivars. Russ. J. Plant Physiol. 66, 214–222. https://doi.org/10.1134/s1021443719020079 (2019).
Google Scholar
Limami, M. A., Sun, L.-Y., Douat, C., Helgeson, J. & Tepfer, D. Natural genetic transformation by__Agrobacterium rhizogenes. Plant Physiol. 118, 543–550 (1998).
Google Scholar
Devlin, P. F., Yanovsky, M. J. & Kay, S. A. A genomic analysis of the shade avoidance response in Arabidopsis. Plant Physiol. 133, 1617–1629. https://doi.org/10.1104/pp.103.034397 (2003).
Google Scholar
Lorenzo, C. D. et al. Shade delays flowering in Medicago sativa. Plant J. 99, 7–22. https://doi.org/10.1111/tpj.14333 (2019).
Google Scholar
Rezazadeh, A., Harkess, R. & Telmadarrehei, T. The effect of light intensity and temperature on flowering and morphology of potted red firespike. Horticulturae https://doi.org/10.3390/horticulturae4040036 (2018).
Google Scholar
Guo, C. et al. OsSIDP366, a DUF1644 gene, positively regulates responses to drought and salt stresses in rice. J. Integr. Plant Biol. 58, 492–502. https://doi.org/10.1111/jipb.12376 (2016).
Google Scholar
Kapolas, G. et al. APRF1 promotes flowering under long days in Arabidopsis thaliana. Plant Sci. 253, 141–153. https://doi.org/10.1016/j.plantsci.2016.09.015 (2016).
Google Scholar
Walla, A. et al. An Acyl-CoA N-Acyltransferase regulates meristem phase change and plant architecture in barley. Plant Physiol. 183, 1088–1109. https://doi.org/10.1104/pp.20.00087 (2020).
Google Scholar
Goto, M. K. A. S. KEGG: Kyoto encyclopedia of genes and genomes. Nucleic Acids Res. 28, 27–30 (2000).
Google Scholar
Source: Ecology - nature.com
