Cited by 420Light effects on plantsSkin Protection and AgingPlant Gene Expression Analysis

The DOI matches its Crossref record; 41 of the 41 references it cites were found in a registry or an index.

Flavonoids Can Protect Maize DNA from the Induction of Ultraviolet Radiation Damage

Open access

Stapleton, A. E., Walbot, V.·1994·Plant Physiology

Open this paper in CoChat — free account Open PDF

Abstract

Diverse flavonoid compounds are widely distributed in angiosperm families. Flavonoids absorb radiation in the ultraviolet (UV) region of the spectrum, and it has been proposed that these compounds function as UV filters. We demonstrate that the DNA in Zea mays plants that contain flavonoids (primarily anthocyanins) is protected from the induction of damage caused by UV radiation relative to the DNA in plants that are genetically deficient in these compounds. DNA damage was measured with a sensitive and simple assay using individual monoclonal antibodies, one specific for cyclobutane pyrimidine dimer damage and the other specific for pyrimidine(6,4)pyrimidone damage.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Integrity signals

Registry

Crossref · 10.1104/pp.105.3.881

Cites

41 of 41 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Molecular Cloning: A Laboratory Manual
Sambrook, J., Fritsch, E., & Maniatis, T. (1989) · UCLA - Biblioteca de Ciencias de la Salud · Cited by 133,589
Randomization Tests
Edgington, E. S., Edgington, E., & Onghena, P. (1964) · Springer eBooks · doi:10.1002/0471667196.ess2169 · Cited by 2,052
Arabidopsis Flavonoid Mutants Are Hypersensitive to UV-B Irradiation.
Li, J., Ou-Lee, T.-M., Raivo, R. A. B. A., Amundson, R., & Last, R. L. (1993) · The Plant Cell · doi:10.1105/tpc.5.2.171 · Cited by 938
DNA REPAIR ENZYMES
Sancar, A., & Sancar, G. B. (1988) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.57.070188.000333 · Cited by 815
UV‐B EFFECTS ON TERRESTRIAL PLANTS
Tevini, M., & Teramura, A. H. (1989) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1989.tb05552.x · Cited by 614
Internal filters: Prospects for UV‐acclimation in higher plants
Caldwell, M. M., Robberecht, R., & Flint, S. D. (1983) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1983.tb04206.x · Cited by 605
THE BIOLOGY OF THE (6–4) PHOTOPRODUCT
MITCHELL, D. L., & NAIRN, R. S. (1989) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1989.tb05578.x · Cited by 592
Effects of Ultraviolet-B Irradiance on Soybean
Mirecki, R. M., & Teramura, A. H. (1984) · PLANT PHYSIOLOGY · doi:10.1104/pp.74.3.475 · Cited by 488
ERYTHEMA AND MELANOGENESIS ACTION SPECTRA OF NORMAL HUMAN SKIN *
Parrish, J. A., Jaenicke, K. F., & Anderson, R. R. (1982) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1982.tb04362.x · Cited by 464
Arabidopsis Flavonoid Mutants Are Hypersensitive to UV-B Irradiation
Li, J., Ou-Lee, T.-M., Raba, R. M., Amundson, R. G., & Last, R. L. (1993) · The Plant Cell · doi:10.2307/3869583 · Cited by 450

Show all 41 references

Research works printed but not linked: 1

Rivin CJ, Zimmer EA, Walbot V (1982) Isolation of DNA. and DNA recombinants from maize. In WF Sheridan, ed, Maize fo;: Biological 445-450 5 0 451-457 1985-1992 47-78 17-29 Downloaded from https://academic.oup.com/plphys/article/105/3/881/6068122 by guest on 22 October 2023

Sorted by citations

Advances in flavonoid research since 1992
Harborne, J. B., & Williams, C. A. (2000) · Phytochemistry · doi:10.1016/s0031-9422(00)00235-1 · Cited by 3,956
Environmental Significance of Anthocyanins in Plant Stress Responses
Chalker‐Scott, L. (1999) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1999.tb01944.x · Cited by 1,631
Molecular Mechanisms of Ultraviolet Radiation‐Induced DNA Damage and Repair
Rastogi, R. P., Richa, Kumar, A., Tyagi, M. B., & Sinha, R. P. (2010) · Journal of Nucleic Acids · doi:10.4061/2010/592980 · Cited by 1,329
“To avoid the deleterious effects of UVR, plants have acquired two main protective strategies; shielding by flavonoids and phenolic compounds [168, 169] and DNA repair by photoreactivation.”
Background
Citrus flavonoids: Molecular structure, biological activity and nutritional properties: A review
Tripoli, E., Guardia, M. L., Giammanco, S., Majo, D. D., & Giammanco, M. (2007) · Food Chemistry · doi:10.1016/j.foodchem.2006.11.054 · Cited by 1,180
Anthocyanins in vegetative tissues: a proposed unified function in photoprotection
Steyn, W. J., Wand, S. J. E., Holcroft, D. M., & Jacobs, G. (2002) · New Phytologist · doi:10.1046/j.1469-8137.2002.00482.x · Cited by 949
Nature′s Swiss Army Knife: The Diverse Protective Roles of Anthocyanins in Leaves
Gould, K. S. (2004) · BioMed Research International · doi:10.1155/s1110724304406147 · Cited by 927
Uses and Properties ofCitrusFlavonoids
Benavente-García, O., Castillo, J., Marín, F. R., Ortuño, A. M., & del Rı́o, J. A. (1997) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf970373s · Cited by 867
Signal Transduction in Responses to UV-B Radiation
Jenkins, G. I. (2009) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.59.032607.092953 · Cited by 723
Arabidopsis Mutants Lacking Phenolic Sunscreens Exhibit Enhanced Ultraviolet-B Injury and Oxidative Damage
Landry, L., Chapple, C. C. S., & Last, R. L. (1995) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.4.1159 · Cited by 613
Effects of ultraviolet radiation on plant cells
Hollósy, F. (2002) · Micron · doi:10.1016/s0968-4328(01)00011-7 · Cited by 574
Plant Secondary Metabolites Produced in Response to Abiotic Stresses Has Potential Application in Pharmaceutical Product Development
Yeshi, K., Crayn, D., Ritmejerytė, E., & Wangchuk, P. (2022) · Molecules · doi:10.3390/molecules27010313 · Cited by 488
DNA DAMAGE AND REPAIR IN PLANTS
Britt, A. B. (1996) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.47.1.75 · Cited by 486
Flavonoid biosynthesis: ‘new’ functions for an ‘old’ pathway
Shirley, B. W. (1996) · Trends in Plant Science · doi:10.1016/s1360-1385(96)80312-8 · Cited by 457
Elevated UV-B radiation reduces genome stability in plants
Ries, G., Heller, W. E., Puchta, H., Sandermann, H., Seidlitz, H. K., & Höhn, B. (2000) · Nature · doi:10.1038/35017595 · Cited by 408
Functional Significance and Induction by Solar Radiation of Ultraviolet-Absorbing Sunscreens in Field-Grown Soybean Crops
Mazza, C. A. D. S., Boccalandro, H. E., Giordano, C. V., Battista, D., Scopel, A. L., & Ballaré, C. L. (2000) · PLANT PHYSIOLOGY · doi:10.1104/pp.122.1.117 · Cited by 356
Recent advances on the roles of flavonoids as plant protective molecules after UV and high light exposure
Ferreyra, M. L. F., Serra, P., & Casati, P. (2021) · Physiologia Plantarum · doi:10.1111/ppl.13543 · Cited by 354
Transcriptome Profiling of Sulfur-Responsive Genes in Arabidopsis Reveals Global Effects of Sulfur Nutrition on Multiple Metabolic Pathways
Maruyama, A., Inoue, E., Watanabe‐Takahashi, A., Yamaya, T., & Takahashi, H. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.102.019802 · Cited by 308
The Effects of Ultraviolet-B Radiation on Plants: A Molecular Perspective
Jordan, B. R. (1996) · Advances in botanical research · doi:10.1016/s0065-2296(08)60057-9 · Cited by 291
Activation of flavonoid biosynthesis by solar radiation in bilberry ( Vaccinium myrtillus L.) leaves
Hohtola, A., Jaakola, L., Riihinen, K., & K�renlampi, S. O. (2004) · Planta · doi:10.1007/s00425-003-1161-x · Cited by 286
DNA repair mechanisms in plants: crucial sensors and effectors for the maintenance of genome integrity
Bray, C. M., & West, C. E. (2005) · New Phytologist · doi:10.1111/j.1469-8137.2005.01548.x · Cited by 287
The apple WD40 protein MdTTG1 interacts with bHLH but not MYB proteins to regulate anthocyanin accumulation
An, X., Tian, Y., Chen, K., Wang, X., & Hao, Y. (2012) · Journal of Plant Physiology · doi:10.1016/j.jplph.2012.01.015 · Cited by 271
Improving the Content of Essential Amino Acids in Crop Plants: Goals and Opportunities
Ufaz, S., & Galili, G. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.118091 · Cited by 268
Mutations in the pale aleurone color1 Regulatory Gene of the Zea mays Anthocyanin Pathway Have Distinct Phenotypes Relative to the Functionally Similar TRANSPARENT TESTA GLABRA1 Gene in Arabidopsis thaliana [W]
Carey, C. C., Strahle, J. T., Selinger, D. A., & Chandler, V. L. (2004) · The Plant Cell · doi:10.1105/tpc.018796 · Cited by 267
Anthocyanins in cereals
Escribano-Bailón, M. T., Santos‐Buelga, C., & Rivas-Gonzalo, J. C. (2004) · Journal of Chromatography A · doi:10.1016/j.chroma.2004.08.152 · Cited by 266
Flavonoid Functions in Plants
Gould, K. S., & Lister, C. E. (2005) · CRC Press eBooks · doi:10.1201/9781420039443.ch8 · Cited by 263
UV-B Promotes Rapid Nuclear Translocation of the Arabidopsis UV-B–Specific Signaling Component UVR8 and Activates Its Function in the Nucleus
Kaiserli, E., & Jenkins, G. I. (2007) · The Plant Cell · doi:10.1105/tpc.107.053330 · Cited by 259
Impact of clock-associated Arabidopsis pseudo-response regulators in metabolic coordination
Fukushima, A., Kusano, M., Nakamichi, N., Kobayashi, M., Hayashi, N., Sakakibara, H., Mizuno, T., & Saito, K. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0900952106 · Cited by 249
Gene Expression Profiling in Response to Ultraviolet Radiation in Maize Genotypes with Varying Flavonoid Content
Casati, P., & Walbot, V. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.022871 · Cited by 249
Self-citation
Flavonoids of Leguminous Plants: Structure, Biological Activity, and Biosynthesis
Aoki, T., Akashi, T., & Ayabe, S. (2000) · Journal of Plant Research · doi:10.1007/pl00013958 · Cited by 246
Analysis of Flavanone 3-Hydroxylase in Arabidopsis Seedlings (Coordinate Regulation with Chalcone Synthase and Chalcone Isomerase)
Pelletier, M. K., & Shirley, B. W. (1996) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.1.339 · Cited by 243
Identification of Nuclear Genes Encoding Chloroplast-Localized Proteins Required for Embryo Development in Arabidopsis
Bryant, N., Lloyd, J. P., Sweeney, C., Myouga, F., & Meinke, D. W. (2010) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.168120 · Cited by 237
Photomorphogenic responses to ultraviolet‐B light
Jenkins, G. I. (2017) · Plant Cell & Environment · doi:10.1111/pce.12934 · Cited by 236
Effect of Postharvest Ultraviolet Irradiation on Resveratrol and Other Phenolics of Cv. Napoleon Table Grapes
Cantos‐Villar, E., García‐Viguera, C., de Pascual‐Teresa, S., & Tomás-Barberán, F. A. (2000) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf0002948 · Cited by 235
Expression Profiling of the Maize Flavonoid Pathway Genes Controlled by Estradiol-Inducible Transcription Factors CRC and P
Bruce, W., Folkerts, O., Garnaat, C., Crasta, O. R., Roth, B., & Bowen, B. (2000) · The Plant Cell · doi:10.1105/tpc.12.1.65 · Cited by 214
A Null Mutation in the First Enzyme of Flavonoid Biosynthesis Does Not Affect Male Fertility in Arabidopsis
Burbulis, I. E., Iacobucci, M., & Shirley, B. W. (1996) · The Plant Cell · doi:10.1105/tpc.8.6.1013 · Cited by 204
Citrus paradisi and Citrus sinensis flavonoids: Their influence in the defence mechanism against Penicillium digitatum
Ortuño, A. M., Báidez, A. G., Gómez, P., Arcas, M. C., Porras, I., Garcı́a-Lidón, A., & del Rı́o, J. A. (2005) · Food Chemistry · doi:10.1016/j.foodchem.2005.06.017 · Cited by 203
Kinetic Properties and Ammonium-dependent Regulation of Cytosolic Isoenzymes of Glutamine Synthetase in Arabidopsis
Ishiyama, K., Inoue, E., Watanabe‐Takahashi, A., Obara, M., Yamaya, T., & Takahashi, H. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m313710200 · Cited by 198
From ozone depletion to agriculture: understanding the role of UV radiation in sustainable crop production
Wargent, J. J., & Jordan, B. R. (2013) · New Phytologist · doi:10.1111/nph.12132 · Cited by 203
Solar Ultraviolet-B Radiation Affects Seedling Emergence, DNA Integrity, Plant Morphology, Growth Rate, and Attractiveness to Herbivore Insects in Datura ferox
Ballaré, C. L., Scopel, A. L., Stapleton, A. E., & Yanovsky, M. J. (1996) · PLANT PHYSIOLOGY · doi:10.1104/pp.112.1.161 · Cited by 196
Self-citation
Effect of Solar Ultraviolet-B Radiation during Springtime Ozone Depletion on Photosynthesis and Biomass Production of Antarctic Vascular Plants
Xiong, F. S., & Day, T. A. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.125.2.738 · Cited by 193
Phenolics as Antioxidants
Grace, S. C. (2005) · Wiley eBooks · doi:10.1002/9780470988565.ch6 · Cited by 192
Contribution of phenolic compounds to the UV-B screening capacity of developing barley primary leaves in relation to DNA damage and repair under elevated UV-B levels
Schmitz-Hoerner, R., & Weissenböck, G. (2003) · Phytochemistry · doi:10.1016/s0031-9422(03)00203-6 · Cited by 189
Anthocyanin-DNA copigmentation complex: mutual protection against oxidative damage
Sarma, A. D., & Sharma, R. P. (1999) · Phytochemistry · doi:10.1016/s0031-9422(99)00427-6 · Cited by 187
An Arabidopsis photolyase mutant is hypersensitive to ultraviolet-B radiation
Landry, L. G., Stapleton, A. E., Lim, J. E., Hoffman, P. D., Hays, J. B., Walbot, V., & Last, R. L. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.1.328 · Cited by 183
Self-citation
An increase in the luteolin : Apigenin ratio in Marchantia polymorpha on UV-B enhancement
Markham, K. R., Ryan, K. G., Bloor, S. J., & Mitchell, K. A. (1998) · Phytochemistry · doi:10.1016/s0031-9422(97)00875-3 · Cited by 173
A flavonoid mutant of barley (Hordeum vulgare L.) exhibits increased sensitivity to UV‐B radiation in the primary leaf
Reuber, S., Bornman, J. F., & Weissenböck, G. (1996) · Plant Cell & Environment · doi:10.1111/j.1365-3040.1996.tb00393.x · Cited by 168
Rapid transcriptome responses of maize (Zea mays) to UV-B in irradiated and shielded tissues
Casati, P., & Walbot, V. (2004) · Genome biology · doi:10.1186/gb-2004-5-3-r16 · Cited by 166
Self-citation
A WD40 Repeat Protein fromMedicago truncatulaIs Necessary for Tissue-Specific Anthocyanin and Proanthocyanidin Biosynthesis But Not for Trichome Development
Pang, Y., Wenger, J. P., Saathoff, K., Peel, G. J., Wen, J., Huhman, D. V., Allen, S. N., Tang, Y., Cheng, X., Tadege, M., et al. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.144022 · Cited by 164
Mitogen-activated protein kinase phosphatase is required for genotoxic stress relief inArabidopsisPreprint
Ulm, R., Revenkova, E., Sansebastiano, G. P. D., Bechtold, N., & Paszkowski, J. (2001) · Genes & Development · doi:10.1101/gad.192601 · Cited by 154
UVR8 in Arabidopsis thaliana regulates multiple aspects of cellular differentiation during leaf development in response to ultraviolet B radiation
Wargent, J. J., Gegas, V. C., Jenkins, G. I., Doonan, J. H., & PAUL, N. D. (2009) · New Phytologist · doi:10.1111/j.1469-8137.2009.02855.x · Cited by 150
Sinapate esters provide greater UV‐B attenuation than flavonoids in Arabidopsis thaliana (Brassicaceae)
Sheahan, J. J. (1996) · American Journal of Botany · doi:10.1002/j.1537-2197.1996.tb12757.x · Cited by 148
Effects of Epidermal Cell Shape and Pigmentation on Optical Properties of Antirrhinum Petals at Visible and Ultraviolet Wavelengths
Gorton, H. L., & Vogelmann, T. C. (1996) · PLANT PHYSIOLOGY · doi:10.1104/pp.112.3.879 · Cited by 145
Plant physiological responses to UV-B radiation
Zlatev, Z. S., Lidon, F. C., & Kaimakanova, M. (2012) · Emirates Journal of Food and Agriculture · doi:10.9755/ejfa.v24i6.14669 · Cited by 144
GLOBAL PATTERNS OF LEAF DEFENSES IN OAK SPECIES
Pearse, I. S., & Hipp, A. L. (2012) · Evolution · doi:10.1111/j.1558-5646.2012.01591.x · Cited by 142
Plant L10 Ribosomal Proteins Have Different Roles during Development and Translation under Ultraviolet-B Stress
Ferreyra, M. L. F., Pezza, A., Biarc, J., Burlingame, A. L., & Casati, P. (2010) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.157057 · Cited by 139
The importance of non-photosynthetic pigments and cinnamic acid derivatives in photoprotection
Edreva, A. M. (2004) · Agriculture Ecosystems & Environment · doi:10.1016/j.agee.2004.10.002 · Cited by 145
Recent Progress in Deciphering the Biosynthesis of Aspartate-Derived Amino Acids in Plants
Jander, G., & Joshi, V. (2009) · Molecular Plant · doi:10.1093/mp/ssp104 · Cited by 139
Ecosystem Consequences of Enhanced Solar Ultraviolet Radiation: Secondary Plant Metabolites as Mediators of Multiple Trophic Interactions in Terrestrial Plant Communities¶
Bassman, J. H. (2004) · Photochemistry and Photobiology · doi:10.1562/si-03-24.1 · Cited by 144
Antisense Inhibition of Threonine Synthase Leads to High Methionine Content in Transgenic Potato Plants
Zeh, M., Casazza, A. P., Kreft, O., Roessner, U., Bieberich, K., Willmitzer, L., Hoefgen, R., & Hesse, H. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.010438 · Cited by 133
The N-Terminal Region of Arabidopsis Cystathionine γ-Synthase Plays an Important Regulatory Role in Methionine Metabolism
Hacham, Y., Avraham, T., & Amir, R. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.010819 · Cited by 133
Influence of PAR and UV-A in Determining Plant Sensitivity and Photomorphogenic Responses to UV-B Radiation¶ †
Krizek, D. T. (2004) · Photochemistry and Photobiology · doi:10.1562/2004-01-27-ir.1 · Cited by 141
Expression of Arabidopsis MYB transcription factor, AtMYB111, in tobacco requires light to modulate flavonol content
Pandey, A. K., Misra, P., Bhambhani, S., Bhatia, C., & Trivedi, P. K. (2014) · Scientific Reports · doi:10.1038/srep05018 · Cited by 132
Repair of UV damage in plants by nucleotide excision repair: Arabidopsis UVH1 DNA repair gene is a homolog of Saccharomyces cerevisiae Rad1
Liu, Z., Hossain, G. S., Islas-Osuna, M. A., Mitchell, D. L., & Mount, D. W. (2000) · The Plant Journal · doi:10.1046/j.1365-313x.2000.00707.x · Cited by 128
Environmentally induced changes in antioxidant phenolic compounds levels in wild plants
Bautista, I., Boşcaiu, M., Lidón, A., Llinares, J. V., Lull, C., Donat-Torres, M. P., García-Berlanga, O. M., & Vicente, Ó. (2015) · Acta Physiologiae Plantarum · doi:10.1007/s11738-015-2025-2 · Cited by 126
Interaction of the Arabidopsis UV-B-Specific Signaling Component UVR8 with Chromatin
Cloix, C., & Jenkins, G. I. (2007) · Molecular Plant · doi:10.1093/mp/ssm012 · Cited by 124
Mutation in the Threonine Synthase Gene Results in an Over-Accumulation of Soluble Methionine in Arabidopsis
Bartlem, D. G., Lambein, I., Okamoto, T., Itaya, A., Uda, Y., Kijima, F., Tamaki, Y., Nambara, E., & Naito, S. (2000) · PLANT PHYSIOLOGY · doi:10.1104/pp.123.1.101 · Cited by 123
When plants produce not enough or at all: metabolic engineering of flavonoids in microbial hosts
Trantas, E., Koffas, M. A. G., Xu, P., & Ververidis, F. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.00007 · Cited by 119
Perturbation of Arabidopsis Amino Acid Metabolism Causes Incompatibility with the Adapted Biotrophic Pathogen Hyaloperonospora arabidopsidis
Stuttmann, J., Hubberten, H., Rietz, S., Kaur, J., Muskett, P. R., Guérois, R., Bednarek, P., Hoefgen, R., & Parker, J. E. (2011) · The Plant Cell · doi:10.1105/tpc.111.087684 · Cited by 116
Drought and UV Radiation Stress Tolerance in Rice Is Improved by Overaccumulation of Non-Enzymatic Antioxidant Flavonoids
Jan, R., Khan, M. A., Asaf, S., Lubna, Waqas, M., Park, J., Asif, S., Kim, N., Lee, I., & Kim, K. (2022) · Antioxidants · doi:10.3390/antiox11050917 · Cited by 114
Differential accumulation of maysin and rhamnosylisoorientin in leaves of high‐altitude landraces of maize after UV‐B exposure
Casati, P., & Walbot, V. (2005) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2005.01329.x · Cited by 113
Self-citation
The effects of long‐term elevated UV‐B on the growth and phenolics of field‐grown silver birch (Betula pendula)
Tegelberg, R., Julkunen‐Tiitto, R., & Aphalo, P. J. (2001) · Global Change Biology · doi:10.1046/j.1354-1013.2001.00453.x · Cited by 110
DNA repair in higher plants; photoreactivation is the major DNA repair pathway in non-proliferating cells while excision repair (nucleotide excision repair and base excision repair) is active in proliferating cells
Kimura, S. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh591 · Cited by 103
Histone Acetylation and Chromatin Remodeling Are Required for UV-B–Dependent Transcriptional Activation of Regulated Genes in Maize
Casati, P., Campi, M., Feixia Chu, C., Suzuki, N., Maltby, D. A., Guan, S., Burlingame, A. L., & Walbot, V. (2008) · The Plant Cell · doi:10.1105/tpc.107.056457 · Cited by 107
Self-citation
Selective sorting of ancestral introgression in maize and teosinte along an elevational cline
Calfee, E., Gates, D. J., Lorant, A., Perkins, M. T., Coop, G., & Ross‐Ibarra, J. (2021) · PLoS Genetics · doi:10.1371/journal.pgen.1009810 · Cited by 102
A WD-repeat-containing putative regulatory protein in anthocyanin biosynthesis in Perilla frutescens
Sompornpailin, K., Makita, Y., Yamazaki, M., & Saito, K. (2002) · Plant Molecular Biology · doi:10.1023/a:1019850921627 · Cited by 104
Silencing CHALCONE SYNTHASE in Maize Impedes the Incorporation of Tricin into Lignin and Increases Lignin Content
Eloy, N. B., Voorend, W., Lan, W., Saleme, M. D. L. S., Cesarino, I., Vanholme, R., Smith, R. A., Goeminne, G., Pallidis, A., Morreel, K., et al. (2016) · PLANT PHYSIOLOGY · doi:10.1104/pp.16.01108 · Cited by 103
Constitutive Overexpression of Cystathionine γ-Synthase in Arabidopsis Leads to Accumulation of Soluble Methionine andS-Methylmethionine
Kim, J., Lee, M., Chalam, R., Martin, M. N., Leustek, T., & Boerjan, W. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.101801 · Cited by 102
Phenylpropanoid compounds in primary leaf tissues of rye (Secale cereale). Light response of their metabolism and the possible role in UV‐B protection
Reuber, S., Bornman, J. F., & Weissenböck, G. (1996) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1996.tb00492.x · Cited by 99
Anthocyanins from Maize (Zea mays) and Reed Canarygrass (Phalaris arundinacea)
Fossen, T., Slimestad, R., & Andersen, Ø. M. (2001) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf001399d · Cited by 98
Sensitivity of Rice to Ultraviolet-B Radiation
Hidema, J., & Kumagai, T. (2006) · Annals of Botany · doi:10.1093/aob/mcl044 · Cited by 97
Mutants of Arabidopsis as Tools to Understand the Regulation of Phenylpropanoid Pathway and UVB Protection Mechanisms
Bharti, A. K., & Khurana, J. P. (1997) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1997.tb01923.x · Cited by 96
Analysis of Leaf Proteome after UV-B Irradiation in Maize Lines Differing in Sensitivity
Casati, P., Zhang, X., Burlingame, A. L., & Walbot, V. (2005) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m500173-mcp200 · Cited by 95
Self-citation
Arabidopsis Methionineγ-Lyase Is Regulated According to Isoleucine Biosynthesis Needs But Plays a Subordinate Role to Threonine Deaminase
Joshi, V., & Jander, G. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.138651 · Cited by 94
UV irradiation Alters the Levels of Flavonoids Involved in the Defence Mechanism of Citrus aurantium Fruits against Penicillium digitatum
Arcas, M. C., Botía, J. M., Ortuño, A. M., & del Rı́o, J. A. (2000) · European Journal of Plant Pathology · doi:10.1023/a:1008704102446 · Cited by 94
UV‐B component of sunlight causes measurable damage in field‐grown maize (Zea mays L.): developmental and cellular heterogeneity of damage and repair
Stapleton, A. E., Thornber, C., & Walbot, V. (1997) · Plant Cell & Environment · doi:10.1046/j.1365-3040.1997.d01-81.x · Cited by 90
Self-citation
Occurrence of tannins in leaves of beech trees (Fagus sylvatica) along an ecological gradient, detected by histochemical and ultrastructural analyses
Bussotti, F., Gravano, E., Grossoni, P., & Tani, C. (1998) · New Phytologist · doi:10.1046/j.1469-8137.1998.00121.x · Cited by 93
Genome‐wide analysis of high‐altitude maize and gene knockdown stocks implicates chromatin remodeling proteins in response to UV‐B
Casati, P., Stapleton, A. E., Blum, J. E., & Walbot, V. (2006) · The Plant Journal · doi:10.1111/j.1365-313x.2006.02721.x · Cited by 92
Self-citation
A REVIEW ON SWEET ORANGE (CITRUS SINENSIS L Osbeck): HEALTH, DISEASES AND MANAGEMENT
Etebu, E., Nwauzoma, A. B., & Norte, A. (2014) · Cited by 92
Purification and Identification of Flavonoids from the Yellow Green Cocoon Shell (Sasamayu) of the Silkworm, Bombyx mori
Kurioka, A., & YAMAZAKI, M. (2002) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.66.1396 · Cited by 92
Regulation of enzymes involved in anthocyanin biosynthesis in carrot cell cultures in response to treatment with ultraviolet light and fungal elicitors
Gläßgen, W. E., Rose, A., Madlung, J., Koch, W., Gleitz, J., & Seitz, H. U. (1998) · Planta · doi:10.1007/s004250050283 · Cited by 92
Functional Characterization of a Methionine -Lyase in Arabidopsis and its Implication in an Alternative to the Reverse Trans-sulfuration Pathway
Goyer, A., Collakova, E., Shachar‐Hill, Y., & Hanson, A. D. (2006) · Plant and Cell Physiology · doi:10.1093/pcp/pcl055 · Cited by 91
Effects of ozone depletion and increased UV‐B on terrestrial ecosystems
Björn, L. O. (1996) · International Journal of Environmental Studies · doi:10.1080/00207239608711082 · Cited by 91
Retracted: Nitric oxide enhances plant ultraviolet‐B protection up‐regulating gene expression of the phenylpropanoid biosynthetic pathway
Tossi, V. E., AMENTA, M., Lamattina, L., & Cassia, R. (2011) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2011.02289.x · Cited by 90
Retracted
Functional Analysis of Cystathionine γ-Synthase in Genetically Engineered Potato Plants
Kreft, O., Hoefgen, R., & Hesse, H. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.102.015933 · Cited by 90
Insertional Inactivation of the Methionine S-Methyltransferase Gene Eliminates the S-Methylmethionine Cycle and Increases the Methylation Ratio
Kocsis, M. G., Ranocha, P., Gage, D. A., Simon, E. S., Rhodes, D., Peel, G. J., Mellema, S., Saito, K., Awazuhara, M., Li, C., et al. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.102.018846 · Cited by 89
Plant Responses to UV Radiation and Links to Pathogen Resistance
Kunz, B. A., Cahill, D. M., Mohr, P. G., Osmond-McLeod, M. J., & Vonarx, E. J. (2006) · International review of cytology · doi:10.1016/s0074-7696(06)55001-6 · Cited by 91
Development in the Floating World: Defenses of Eggs and Embryos Against Damage from UV Radiation
Epel, D. D., HEMELA, K., Shick, M., & Patton, C. W. (1999) · American Zoologist · doi:10.1093/icb/39.2.271 · Cited by 88
Short term UV-B radiation-mediated transcriptional responses and altered secondary metabolism of in vitro propagated plantlets of Artemisia annua L.
Pandey, N., & Rai, S. P. (2013) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-013-0413-0 · Cited by 87
Polyphenols: Major regulators of key components of DNA damage response in cancer
Majidinia, M., Bishayee, A., & Yousefi, B. (2019) · DNA repair · doi:10.1016/j.dnarep.2019.102679 · Cited by 87
Flavonoids as nutraceuticals: Structural related antioxidant properties and their role on ascorbic acid preservation
Marín, F. R., Fernández, M. J. F., Pérez‐Álvarez, J. Á., Martinez-Sánchez, F., & del Rı́o, J. A. (2002) · Studies in natural products chemistry · doi:10.1016/s1572-5995(02)80018-7 · Cited by 85

Authors: Stapleton, A. E., & Walbot, V.
Affiliations: Stanford University (US)
ORCID: Stapleton, A. E.
Walbot, V.
Venue: Plant Physiology
Publisher: Oxford University Press (OUP)
Published: 1994-07-01
Volume: 105
Issue: 3
Pages: 881-889
ISSN: 0032-0889 (ISSN-L)
1532-2548
DOI: 10.1104/pp.105.3.881
PMC: PMC160736
OpenAlex: W2120833079
Cited by: 420
References: 41
Citations by year: 2026: 1 · 2025: 13 · 2024: 8 · 2023: 8 · 2022: 11 · 2021: 11 · 2020: 9 · 2019: 10 · 2018: 9 · 2017: 14 · 2016: 14 · 2015: 15 · 2014: 9 · 2013: 10 · 2012: 18
FWCI: 16.84
Type: journal article
Language: en
Open access: bronze
doi.org
Licence: aspb.org/publications/aspb-journals/open-articles (vor, 365 d)
Locations: PLANT PHYSIOLOGY (publishedVersion)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
Funders: National Institutes of Health (1f32es005545-01)
National Institute of Environmental Health Sciences (F32 ES05545)
Topics: Life Sciences › Agricultural and Biological Sciences › Plant Science › Light effects on plants
Health Sciences › Medicine › Dermatology › Skin Protection and Aging
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Plant Gene Expression Analysis
Keywords: flavonoids, anthocyanins, maize, ultraviolet radiation, DNA damage, UV protection, cyclobutane pyrimidine dimers, monoclonal antibodies, UV filters
MeSH terms: Anthocyanins, Zea mays, DNA, DNA Damage, Dose-Response Relationship, Radiation, Flavonoids, Kinetics, Ultraviolet Rays

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Flavonoids Can Protect Maize DNA from the Induction of Ultraviolet Radiation Damage

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks