Cited by 99Photosynthetic Processes and MechanismsPlant nutrient uptake and metabolismPlant Stress Responses and Tolerance

The DOI matches its Crossref record; 49 of the 49 references it cites were found in a registry or an index.

Characterization of an Arabidopsis thaliana mutant lacking a cytosolic non-phosphorylating glyceraldehyde-3-phosphate dehydrogenase

Open access

Rius, Sebastián P., Casati, Paula, Iglesias, Alberto A., Gomez-Casati, Diego F.·2006·Plant Molecular Biology

DOI 10.1007/s11103-006-0060-5

Open this paper in CoChat — free account

Abstract

Non-phosphorylating glyceraldehyde- 3-phosphate dehydrogenase (NP-GAPDH) is a conserved cytosolic protein found in higher plants. In photosynthetic cells, the enzyme is involved in a shuttle transfer mechanism to export NADPH from the chloroplast to the cytosol. To investigate the role of this enzyme in plant tissues, we characterized a mutant from Arabidopsis thaliana having an insertion at the NP-GAPDH gene locus. The homozygous mutant was determined to be null respect to NP-GAPDH, as it exhibited undetectable levels of both transcription of NP-GAPDH mRNA, protein expression and enzyme activity. Transcriptome analysis demonstrated that the insertion mutant plant shows altered expression of several enzymes involved in carbohydrate metabolism. Significantly, cytosolic phosphorylating (NAD-dependent) glyceraldehyde-3-phosphate dehydrogenase mRNA levels are induced in the mutant, which correlates with an increase in enzyme activity. mRNA levels and enzymatic activity of glucose-6-phosphate dehydrogenase were also elevated, correlating with an increase in NADPH concentration. Moreover, increased ROS levels were measured in the mutant plants. Down-regulation of several glycolytic and photosynthetic genes suggests that NP-GAPDH is important for the efficiency of both metabolic processes. The results presented demonstrate that NP-GAPDH has a relevant role in plant growth and development.

Integrity signals

Registry

Crossref · 10.1007/s11103-006-0060-5

Cites

49 of 49 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

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?

Molecular Cloning: A Laboratory Manual
Sambrook, J., Fritsch, E., & Maniatis, T. (1989) · UCLA - Biblioteca de Ciencias de la Salud · Cited by 133,589
In silico prediction of protein-protein interactions in human macrophages
Souiai, O., Guerfali, F. Z., Miled, S. B., Brun, C., & Benkahla, A. (2014) · BMC Research Notes · doi:10.1186/1756-0500-7-157 · Cited by 10,785
Significance analysis of microarrays applied to the ionizing radiation response
Tusher, V. G., Tibshirani, R., & Chu, G. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.091062498 · Cited by 10,568
A comparison of normalization methods for high density oligonucleotide array data based on variance and bias
Bolstad, B. M., Irizarry, R. A., Åstrand, M., & Speed, T. P. (2003) · Bioinformatics · doi:10.1093/bioinformatics/19.2.185 · Cited by 8,357
Assaying for superoxide dismutase activity: Some large consequences of minor changes in conditions
Beyer, W. F., & Fridovich, I. (1987) · Analytical Biochemistry · doi:10.1016/0003-2697(87)90489-1 · Cited by 2,944
P LANT M ITOCHONDRIA AND O XIDATIVE S TRESS : Electron Transport, NADPH Turnover, and Metabolism of Reactive Oxygen Species
Møller, I. M. (2001) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.52.1.561 · Cited by 1,693
[10] Superoxide dismutase assays
Flohé, L., & Ötting, F. (1984) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(84)05013-8 · Cited by 1,509
Extinction Coefficients of Chlorophyll a and b in N,N -Dimethylformamide and 80% Acetone
Inskeep, W. P., & Bloom, P. R. (1985) · PLANT PHYSIOLOGY · doi:10.1104/pp.77.2.483 · Cited by 1,403
Respiratory metabolism: glycolysis, the TCA cycle and mitochondrial electron transport
Fernie, A. R., Carrari, F., & Sweetlove, L. J. (2004) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2004.03.007 · Cited by 1,403
Formulae for Determination of Chlorophyllous Pigments Extracted with N,N -Dimethylformamide
Moran, R. (1982) · PLANT PHYSIOLOGY · doi:10.1104/pp.69.6.1376 · Cited by 1,250

Show all 49 references

Research works printed but not linked: 1

Bollag DM, Edelstein SJ (1991) Protein concentration determination. In: Bollag DM, Edelstein SJ (eds). Protein methods. Wiley-Liss, New York, pp 50–55

Redox Regulation in Photosynthetic Organisms: Signaling, Acclimation, and Practical Implications
Foyer, C. H., & Noctor, G. (2008) · Antioxidants and Redox Signaling · doi:10.1089/ars.2008.2177 · Cited by 1,474
Beyond Glycolysis: GAPDHs Are Multi-functional Enzymes Involved in Regulation of ROS, Autophagy, and Plant Immune Responses
Henry, E. M., Fung, N., Liu, J., Drakakaki, G., & Coaker, G. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005199 · Cited by 411
Nitric Oxide and ProteinS-Nitrosylation Are Integral to Hydrogen Peroxide-Induced Leaf Cell Death in Rice
Lin, A., Wang, Y., Tang, J., Xue, P., Li, C., Liu, L., Hu, B., Yang, F., Loake, G. J., & Chu, C. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.184531 · Cited by 353
The metabolomics of oxidative stress
Noctor, G., Lelarge‐Trouverie, C., & Mhamdi, A. (2014) · Phytochemistry · doi:10.1016/j.phytochem.2014.09.002 · Cited by 265
Cytosolic Glyceraldehyde-3-Phosphate Dehydrogenases Interact with Phospholipase Dδ to Transduce Hydrogen Peroxide Signals in the Arabidopsis Response to Stress
Guo, L., Devaiah, S. P., Narasimhan, R., Pan, X., Zhang, Y., Zhang, W., & Wang, X. (2012) · The Plant Cell · doi:10.1105/tpc.111.094946 · Cited by 239
Cytoplastic Glyceraldehyde-3-Phosphate Dehydrogenases Interact with ATG3 to Negatively Regulate Autophagy and Immunity in Nicotiana benthamiana
Han, S., Wang, Y., Zheng, X., Jia, Q., Zhao, J., Bai, F., Hong, Y., & Liu, Y. (2015) · The Plant Cell · doi:10.1105/tpc.114.134692 · Cited by 208
Plant cytoplasmic GAPDH: redox post-translational modifications and moonlighting properties
Zaffagnini, M., Fermani, S., Costa, A., Lemaire, S. D., & Trost, P. (2013) · Frontiers in Plant Science · doi:10.3389/fpls.2013.00450 · Cited by 205
Multiple strategies to prevent oxidative stress in Arabidopsis plants lacking the malate valve enzyme NADP-malate dehydrogenase
Hebbelmann, I., Selinski, J., Wehmeyer, C., Goss, T., Voß, I., Mulo, P., Kangasjärvi, S., Aro, E., Oelze, M.-L., Dietz, K., et al. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/err386 · Cited by 154
Glutathionylation of cytosolic glyceraldehyde-3-phosphate dehydrogenase from the model plant Arabidopsis thaliana is reversed by both glutaredoxins and thioredoxins in vitro
Bedhomme, M., Adamo, M., Marchand, C. H., Couturier, J., Rouhier, N., Lemaire, S. D., Zaffagnini, M., & Trost, P. (2012) · Biochemical Journal · doi:10.1042/bj20120505 · Cited by 147
Characterization of Arabidopsis Lines Deficient in GAPC-1, a Cytosolic NAD-Dependent Glyceraldehyde-3-Phosphate Dehydrogenase
Rius, S. P., Casati, P., Iglesias, A. Á., & Gomez‐Casati, D. F. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.128769 · Cited by 136
Self-citation
Cytosolic NADP-dependent isocitrate dehydrogenase contributes to redox homeostasis and the regulation of pathogen responses inArabidopsisleaves
Mhamdi, A., Mauve, C., Gouia, H., Saindrenan, P., Hodges, M., & Noctor, G. (2010) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2010.02133.x · Cited by 133
Redox-shuttling between chloroplast and cytosol: integration of intra-chloroplast and extra-chloroplast metabolism
Taniguchi, M., & Miyake, H. (2012) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2012.01.014 · Cited by 132
Leaf Energy Balance Requires Mitochondrial Respiration and Export of Chloroplast NADPH in the Light
Shameer, S., Ratcliffe, R. G., & Sweetlove, L. J. (2019) · Plant Physiology · doi:10.1104/pp.19.00624 · Cited by 118
Nuclear moonlighting of cytosolic glyceraldehyde-3-phosphate dehydrogenase regulates Arabidopsis response to heat stress
Kim, S., Guo, L., & Wang, X. (2020) · Nature Communications · doi:10.1038/s41467-020-17311-4 · Cited by 114
Phosphoglycerate Kinases Are Co-Regulated to Adjust Metabolism and to Optimize Growth
Rosa‐Téllez, S., Anoman, A. D., Flores‐Tornero, M., Toujani, W., Alseek, S., Fernie, A. R., Nebauer, S. G., Muñoz‐Bertomeu, J., Segura, J., & Ros, R. (2017) · PLANT PHYSIOLOGY · doi:10.1104/pp.17.01227 · Cited by 105
High CO2 primes plant biotic stress defences through redox-linked pathways
Mhamdi, A., & Noctor, G. (2016) · PLANT PHYSIOLOGY · doi:10.1104/pp.16.01129 · Cited by 101
Cytosolic Phosphorylating Glyceraldehyde-3-Phosphate Dehydrogenases Affect Arabidopsis Cellular Metabolism and Promote Seed Oil Accumulation
Guo, L., Ma, F., Wei, F., Fanella, B., Allen, D. K., & Wang, X. (2014) · The Plant Cell · doi:10.1105/tpc.114.126946 · Cited by 94
Genome-wide identification and characterization of Glyceraldehyde-3-phosphate dehydrogenase genes family in wheat (Triticum aestivum)
Zeng, L., Deng, R., Guo, Z., Yang, S., & Deng, X. (2016) · BMC Genomics · doi:10.1186/s12864-016-2527-3 · Cited by 91
Recent Development on Plant Aldehyde Dehydrogenase Enzymes and Their Functions in Plant Development and Stress Signaling
Tola, A. J., Jaballi, A., Germain, H., & Missihoun, T. D. (2020) · Genes · doi:10.3390/genes12010051 · Cited by 90
Analyzing the Function of Catalase and the Ascorbate–Glutathione Pathway in H 2 O 2 Processing: Insights from an Experimentally Constrained Kinetic Model
Tuzet, A., Rahantaniaina, M.-S., & Noctor, G. (2018) · Antioxidants and Redox Signaling · doi:10.1089/ars.2018.7601 · Cited by 87
Feedback regulation of photosynthetic electron transport by NADP(H) redox poise
Hald, S., Nandha, B., Gallois, P., & Johnson, G. N. (2008) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2008.02.007 · Cited by 82
Comparative Proteomics Analysis of the Seedling Root Response of Drought-sensitive and Drought-tolerant Maize Varieties to Drought Stress
Zeng, W., Peng, Y., Zhao, X., Wu, B., Chen, F., Ren, B., Zhuang, Z., Gao, Q., & Ding, Y. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20112793 · Cited by 77
Physiological and transcriptional analyses of developmental stages along sugarcane leaf
Mattiello, L., Riaño‐Pachón, D. M., Martins, M. C. M., da Cruz, L. P., Bassi, D., Marchiori, P. E. R., Ribeiro, R. V., Labate, M. T. V., Labate, C. A., & Menossi, M. (2015) · BMC Plant Biology · doi:10.1186/s12870-015-0694-z · Cited by 71
Receptor protein kinase FERONIA controls leaf starch accumulation by interacting with glyceraldehyde-3-phosphate dehydrogenase
Yang, T., Wang, L., Li, C., Liu, Y., Zhu, S., Qi, Y., Liu, X., Lin, Q., Luan, S., & Yu, F. (2015) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2015.07.132 · Cited by 66
Proteome Analysis of Peroxisomes from Etiolated Arabidopsis Seedlings Identifies a Peroxisomal Protease Involved in β-Oxidation and Development
Quan, S., Yang, P., Cassin-Ross, G., Kaur, N., Switzenberg, R., Aung, K., Li, J., & Hu, J. (2013) · PLANT PHYSIOLOGY · doi:10.1104/pp.113.223453 · Cited by 64
Suppression of the External Mitochondrial NADPH Dehydrogenase, NDB1, in Arabidopsis thaliana Affects Central Metabolism and Vegetative Growth
Wallström, S. V., Florez‐Sarasa, I., Araújo, W. L., Aidemark, M., Fernández, M. F., Fernie, A. R., Ribas‐Carbó, M., & Rasmusson, A. G. (2013) · Molecular Plant · doi:10.1093/mp/sst115 · Cited by 55
Nonphosphorylating Glyceraldehyde-3-Phosphate Dehydrogenase Is Phosphorylated in Wheat Endosperm at Serine-404 by an SNF1-Related Protein Kinase Allosterically Inhibited by Ribose-5-Phosphate
Piattoni, C. V., Bustos, D. M., Guerrero, S. A., & Iglesias, A. Á. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.177261 · Cited by 54
Self-citation
Tyr‐Asp inhibition of glyceraldehyde 3‐phosphate dehydrogenase affects plant redox metabolism
Moreno, J. C., Rojas, B. E., Vicente, R., Górka, M., Matz, T. W., Chodasiewicz, M., Peralta‐Ariza, J. S., Zhang, Y., Alseekh, S., Childs, D., et al. (2021) · The EMBO Journal · doi:10.15252/embj.2020106800 · Cited by 52
Self-citation
The mitochondrial protein frataxin is essential for heme biosynthesis in plants
Maliandi, M. V., Busi, M. V., Turowski, V. R., Leaden, L., Araya, A., & Gomez‐Casati, D. F. (2010) · FEBS Journal · doi:10.1111/j.1742-4658.2010.07968.x · Cited by 49
Self-citation
Plants Utilize a Highly Conserved System for Repair of NADH and NADPH Hydrates
Niehaus, T. D., Richardson, L. G. L., Gidda, S. K., Elbadawi-Sidhu, M., Meissen, J. K., Mullen, R. T., Fiehn, O., & Hanson, A. D. (2014) · PLANT PHYSIOLOGY · doi:10.1104/pp.114.236539 · Cited by 48
The Mitochondrial External NADPH Dehydrogenase Modulates the Leaf NADPH/NADP+ Ratio in Transgenic Nicotiana sylvestris
Liu, Y., Norberg, F. E. B., Szilágyi, A., Paepe, R. D., Åkerlund, H., & Rasmusson, A. G. (2008) · Plant and Cell Physiology · doi:10.1093/pcp/pcn001 · Cited by 48
Maintaining homeostasis by controlled alternatives for energy distribution in plant cells under changing conditions of supply and demand
Scheibe, R. (2018) · Photosynthesis Research · doi:10.1007/s11120-018-0583-z · Cited by 47
Functional Characterization of the Plastidic Phosphate Translocator Gene Family from the Thermo-Acidophilic Red Alga Galdieria sulphuraria Reveals Specific Adaptations of Primary Carbon Partitioning in Green Plants and Red Algae
Linka, M., Jamaï, A., & Weber, A. P. M. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.129478 · Cited by 47
A Redox-Mediated Modulation of Stem Bolting in Transgenic Nicotiana sylvestris Differentially Expressing the External Mitochondrial NADPH Dehydrogenase
Liu, Y., Nunes‐Nesi, A., Wallström, S. V., Lager, I., Michalecka, A. M., Norberg, F. E. B., Widell, S., Fredlund, K. M., Fernie, A. R., & Rasmusson, A. G. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.136242 · Cited by 47
Involvement of mitochondria in the control of plant cell NAD(P)H reduction levels
Rasmusson, A. G., & Wallström, S. V. (2010) · Biochemical Society Transactions · doi:10.1042/bst0380661 · Cited by 44
A Differential Redox Regulation of the Pathways Metabolizing Glyceraldehyde-3-Phosphate Tunes the Production of Reducing Power in the Cytosol of Plant Cells
Piattoni, C. V., Guerrero, S. A., & Iglesias, A. Á. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms14048073 · Cited by 42
Self-citation
Biosynthesis of NAD and Its Manipulation in Plants☆
Noctor, G., Hager, J., & Li, S. (2011) · Advances in botanical research · doi:10.1016/b978-0-12-386479-6.00002-0 · Cited by 40
A light switch based on protein S-nitrosylation fine-tunes photosynthetic light-harvesting in the microalga Chlamydomonas reinhardtii
Berger, H., de Mia, M., Morisse, S., Marchand, C., Lemaire, S. D., Wobbe, L., & Kruse, O. (2016) · PLANT PHYSIOLOGY · doi:10.1104/pp.15.01878 · Cited by 40
Molecular identification of GAPDHs in cassava highlights the antagonism of MeGAPCs and MeATG8s in plant disease resistance against cassava bacterial blight
Zeng, H., Xie, Y., Liu, G., Lin, D., He, C., & Shi, H. (2018) · Plant Molecular Biology · doi:10.1007/s11103-018-0733-x · Cited by 39
Effect of Mitochondrial Dysfunction on Carbon Metabolism and Gene Expression in Flower Tissues of Arabidopsis thaliana
Busi, M. V., Lobato, M. E. G., Rius, S. P., Turowski, V. R., Casati, P., Zabaleta, E. J., Gomez‐Casati, D. F., & Araya, A. (2010) · Molecular Plant · doi:10.1093/mp/ssq065 · Cited by 39
Self-citation
Reconstruction of Oryza sativa indica Genome Scale Metabolic Model and Its Responses to Varying RuBisCO Activity, Light Intensity, and Enzymatic Cost Conditions
Chatterjee, A., Huma, B., Shaw, R., & Kundu, S. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.02060 · Cited by 33
Analysis of knockout mutants suggests that Arabidopsis NADP-MALIC ENZYME2 does not play an essential role in responses to oxidative stress of intracellular or extracellular origin
Li, S., Mhamdi, A., Clement, C., Jolivet, Y., & Noctor, G. (2013) · Journal of Experimental Botany · doi:10.1093/jxb/ert194 · Cited by 33
How volatile isoprenoids improve plant thermotolerance
Zuo, Z., Weraduwage, S. M., Huang, T., & Sharkey, T. D. (2025) · Trends in Plant Science · doi:10.1016/j.tplants.2025.05.004 · Cited by 32
Genome-scale in silico modeling and analysis for designing synthetic terpenoid-producing microbial cell factories
Chung, B. K.-S., Lakshmanan, M., Klement, M., Mohanty, B., & Lee, D. (2012) · Chemical Engineering Science · doi:10.1016/j.ces.2012.09.006 · Cited by 29
Differential blockage of photosynthetic electron flow in young and mature leaves of Arabidopsis thaliana by exogenous proline
Sperdouli, I., & Moustakas, M. (2015) · Photosynthetica · doi:10.1007/s11099-015-0116-3 · Cited by 29
Cytosolic GAPDH: a key mediator in redox signal transduction in plants
Yang, S. S., & Zhai, Q. H. (2017) · Biologia Plantarum · doi:10.1007/s10535-017-0706-y · Cited by 28
Analysis of the roles of the Arabidopsis peroxisomal isocitrate dehydrogenase in leaf metabolism and oxidative stress
Mhamdi, A., & Noctor, G. (2014) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2014.07.002 · Cited by 27
Comparative Transcriptome Analysis of Primary Roots of Brassica napus Seedlings with Extremely Different Primary Root Lengths Using RNA Sequencing
Dun, X., Tao, Z., Wang, J., Wang, X., Liu, G., & Wang, H. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.01238 · Cited by 26
A cytosolic oxidation–reduction cycle in plant leaves
Wieloch, T. (2021) · Journal of Experimental Botany · doi:10.1093/jxb/erab128 · Cited by 24
A phloem-limited fijivirus induces the formation of neoplastic phloem tissues that house virus multiplication in the host plant
Shen, J., Chen, X., Chen, J., & Sun, L. (2016) · Scientific Reports · doi:10.1038/srep29848 · Cited by 24
The Cryptic Plastid of Euglena longa Defines a New Type of Nonphotosynthetic Plastid Organelle
Füssy, Z., Záhonová, K., Tomčala, A., Krajčovič, J., Yurchenko, V., Oborník, M., & Eliáš, M. (2020) · mSphere · doi:10.1128/msphere.00675-20 · Cited by 23
Overexpression of cytoplasmicSolanum tuberosumGlyceraldehyde 3-phosphate dehydrogenase (GAPDH) gene improves PSII efficiency and alleviates salinity stress inArabidopsis.
Kappachery, S., Sasi, S., Alyammahi, O., Alyassi, A., Venkatesh, J., & Gururani, M. A. (2021) · Journal of Plant Interactions · doi:10.1080/17429145.2021.1962420 · Cited by 22
Beyond glycolysis: multifunctional roles of glyceraldehyde-3-phosphate dehydrogenases in plants
Cao, Y., Hong, J., Wang, H., Lin, M., Cai, Y., Liao, L., Li, X., & Han, Y. (2025) · Horticulture Research · doi:10.1093/hr/uhaf070 · Cited by 21
From algae to vascular plants: The multistep evolutionary trajectory of the ALDH superfamily towards functional promiscuity and the emergence of structural characteristics
Stiti, N., Giarola, V., & Bartels, D. (2021) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2021.104376 · Cited by 20
Seasonal below‐ground metabolism in switchgrass
Palmer, N. A., Saathoff, A. J., Scully, E. D., Tobias, C. M., Twigg, P., Madhavan, S., Schmer, M. R., Cahoon, R. E., Sattler, S. E., Edmé, S. J., et al. (2017) · The Plant Journal · doi:10.1111/tpj.13742 · Cited by 20
Chapter 8 Use of Transgenic Plants to Uncover Strategies for Maintenance of Redox Homeostasis During Photosynthesis
HANKE, G. T., Holtgrefe, S., König, N., Strodtkötter, I., Voß, I., & Scheibe, R. (2009) · Advances in botanical research · doi:10.1016/s0065-2296(10)52008-1 · Cited by 20
The isoprene‐responsive phosphoproteome provides new insights into the putative signalling pathways and novel roles of isoprene
Weraduwage, S. M., Whitten, D. A., Kulke, M., Sahu, A., Vermaas, J. V., & Sharkey, T. D. (2023) · Plant Cell & Environment · doi:10.1111/pce.14776 · Cited by 19
Proteogenic Dipeptides Are Characterized by Diel Fluctuations and Target of Rapamycin Complex-Signaling Dependency in the Model Plant Arabidopsis thaliana
Calderan‐Rodrigues, M. J., Luzarowski, M., Monte‐Bello, C. C., Minen, R. I., Zühlke, B. M., Nikoloski, Z., Skirycz, A., & Caldana, C. (2021) · Frontiers in Plant Science · doi:10.3389/fpls.2021.758933 · Cited by 15
The ALDH 21 gene found in lower plants and some vascular plants codes for a NADP +‐dependent succinic semialdehyde dehydrogenase
Kopečná, M., Vigouroux, A., Vilím, J., Končitíková, R., Briozzo, P., Hájková, E., Jašková, L., von Schwartzenberg, K., Šebela, M., Moréra, S., et al. (2017) · The Plant Journal · doi:10.1111/tpj.13648 · Cited by 15
Co-expression network and comparative transcriptome analysis for fiber initiation and elongation reveal genetic differences in two lines from upland cotton CCRI70 RIL population
Jiang, X., Fan, L., Li, P., Zou, X., Zhang, Z., Fan, S., Gōng, J., Yuán, Y., & Shāng, H. (2021) · PeerJ · doi:10.7717/peerj.11812 · Cited by 14
Reprogramming the translatome during daily light transitions as affected by cytosolic glyceraldehyde-3-phosphate dehydrogenases GAPC1/C2
Wegener, M., Persicke, M., & Dietz, K. (2023) · Journal of Experimental Botany · doi:10.1093/jxb/erad509 · Cited by 13
Quantitative proteomics suggests changes in the carbohydrate metabolism of maize in response to larvae of the belowground herbivore Holotrichia parallela
Pan, Y., Zhao, S., Wang, Z., Wang, X. Q., Zhang, X., Lee, Y., & Xi, J. (2020) · PeerJ · doi:10.7717/peerj.9819 · Cited by 13
Characteristics and functions of glyceraldehyde 3-phosphate dehydrogenase S-nitrosylation during controlled aging of elm and Arabidopsis seeds
Zeng, M., He, Y., Gao, X., Wang, Y., Deng, S., Ye, T., Wang, X., & Xue, H. (2021) · Journal of Experimental Botany · doi:10.1093/jxb/erab322 · Cited by 11
Evidence for dual targeting control of Arabidopsis 6-phosphogluconate dehydrogenase isoforms by N-terminal phosphorylation
Doering, L. N., Gerling, N., Linnenbrügger, L., Lansing, H., Baune, M., Fischer, K., & von Schaewen, A. (2024) · Journal of Experimental Botany · doi:10.1093/jxb/erae077 · Cited by 9
Hydrogen peroxide in plants
Mhamdi, A. (2022) · Advances in botanical research · doi:10.1016/bs.abr.2022.11.002 · Cited by 9
A Specific Protective Mechanism Against Chloroplast Photo‐Reactive Oxygen Species in Phosphate‐Starved Rice Plants
Xu, Z. (2023) · Advanced Biology · doi:10.1002/adbi.202300106 · Cited by 9
Compartment-specific energy requirements of photosynthetic carbon metabolism in Camelina sativa leaves
Wieloch, T., & Sharkey, T. D. (2022) · Planta · doi:10.1007/s00425-022-03884-5 · Cited by 9
Heterologous expression of non-phosphorylating glyceraldehyde-3-phosphate dehydrogenase from Triticum aestivum and Arabidopsis thaliana
Piattoni, C. V., Rius, S. P., Gomez‐Casati, D. F., Guerrero, S. A., & Iglesias, A. Á. (2010) · Biochimie · doi:10.1016/j.biochi.2010.03.017 · Cited by 9
Self-citation
Identification and expression profiling of GAPDH family genes involved in response to Sclerotinia sclerotiorum infection and phytohormones in Brassica napus
Xu, J., Wang, R., Zhang, X., Zhuang, W., Zhang, Y., Lin, J., Zhan, P., Chen, S., Lu, H., Wang, A., et al. (2024) · Frontiers in Plant Science · doi:10.3389/fpls.2024.1360024 · Cited by 8
Mechanisms of salt tolerance: insights into photosystem function and carbon metabolism in tomato seedlings
Li, X., Han, Y., Cong, Y., Wang, L., Shi, Y., Liu, H., & Liu, H. (2025) · Plant and Soil · doi:10.1007/s11104-025-07810-y · Cited by 7
Proline Biostimulation Enhances Freezing Stress Tolerance in Citrus Through Coordinated Regulation of Photosynthetic Stability, Antioxidant Defense, and Carbohydrate Metabolism
Aucique‐Pérez, C. E., Iqbal, S., Balal, R. M., Chater, J. M., & Shahid, M. A. (2026) · Journal of the American Society for Horticultural Science · doi:10.21273/jashs05536-25 · Cited by 7
Molecular cloning and functional characterization of a glyceraldehyde-3-phosphate dehydrogenase gene from Spartina alterniflora reveals its involvement in salt stress response
Yuan, H., Cai, L., Wang, P., Sun, B., Xu, S., Xia, B., & Wang, R. (2019) · Acta Physiologiae Plantarum · doi:10.1007/s11738-019-2916-8 · Cited by 7
Evidence that tolerance of Eutrema salsugineum to low phosphate conditions is hard-wired by constitutive metabolic and root-associated adaptations
Velasco, V. M. E., Irani, S., Axakova, A., da Silva, R., Summers, P. S., & Weretilnyk, E. A. (2019) · Planta · doi:10.1007/s00425-019-03314-z · Cited by 7
The distinctive level of interaction between carbon and nitrogen metabolisms in the leaves of submerged macrophytes plays a key role in ammonium detoxification
Muthui, S. W., Li, W., Ochieng, W. A., Linda, E. L., Otieno, D. O., Waswa, E. N., Liu, F., & Xian, L. (2024) · Aquatic Toxicology · doi:10.1016/j.aquatox.2024.106840 · Cited by 6
An unusual effect of NADP+ on the thermostability of the nonphosphorylating glyceraldehyde-3-phosphate dehydrogenase from Streptococcus mutans
Arutyunov, D., Schmalhausen, E. V., Orlov, V. N., Rahuel-Clermont, S., Nagradova, N. K., Branlant, G., & Muronetz, V. I. (2013) · Biochemistry and Cell Biology · doi:10.1139/bcb-2012-0104 · Cited by 6
Comparative proteomic analysis of differentially expressed proteins related to phloem and xylem development in rubber tree (Hevea brasiliensis)
Prasongsansuk, P., Thiangtrongjit, T., Nirapathpongporn, K., Viboonjun, U., Kongsawadworakul, P., Reamtong, O., & Narangajavana, J. (2020) · Trees · doi:10.1007/s00468-020-02019-1 · Cited by 6
Mapping the castor bean endosperm proteome revealed a metabolic interaction between plastid, mitochondria, and peroxisomes to optimize seedling growth
Wrobel, T. J., Brilhaus, D., Stefanski, A., Stühler, K., Weber, A. P. M., & Linka, N. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2023.1182105 · Cited by 6
Comparative proteomic analysis of durum wheat shoots from modern and ancient cultivars
Rocco, M., Tartaglia, M., Izzo, F. P., Varricchio, E., Arena, S., Scaloni, A., & Marra, M. (2018) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2018.12.010 · Cited by 6
Roles of Reactive Carbonyl Species (RCS) in Plant Response to Abiotic Stress
Sonmez, M. C., YİRMİBEŞOĞLU, S. S. S., Ozgur, R., Uzilday, B., & Türkan, İ. (2024) · Methods in molecular biology · doi:10.1007/978-1-0716-3826-2_7 · Cited by 5
Analysis of SI-Related BoGAPDH Family Genes and Response of BoGAPC to SI Signal in Brassica oleracea L.
Xie, Q., Zhang, H., Deng-Ke, H. U., Liu, Q., Zuo, T., Zhang, Y., Liu, Y., Zhou, S., & Zhu, L. (2021) · Genes · doi:10.3390/genes12111719 · Cited by 5
Overexpression of Cytosolic Glyceraldehyde-3-Phosphate Dehydrogenase 1 Gene Improves Nitrogen Absorption and Utilization in Potato
Liu, J., Song, J., Zhuang, X., Lu, Y., Wang, Q., Yang, S., Lu, L., Wang, X., & Li, L. (2023) · Horticulturae · doi:10.3390/horticulturae9101105 · Cited by 5
The Multifaceted Connections Between Photosynthesis and Respiratory Metabolism
da Fonseca‐Pereira, P., Batista‐Silva, W., Nunes‐Nesi, A., Zsögön, A., & Araújo, W. L. (2020) · Springer eBooks · doi:10.1007/978-981-15-5228-1_3 · Cited by 3
Cold adaptation of harmful dinoflagellate facilitates their poleward colonization: Insights into extracellular polymeric substances and intracellular bio-macromolecules dynamics through in-situ FTIR imaging
Guo, H., Song, L., Wang, X., Huang, J., Zhang, X., Zhang, Y., Zhu, W., Song, W., Chen, H., Bo, J., et al. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.143054 · Cited by 2
The cryptic plastid of Euglena longa defines a new type of non-photosynthetic plastid organellesPreprint
Füssy, Z., Záhonová, K., Tomčala, A., Krajčovič, J., Yurchenko, V., Oborník, M., & Eliáš, M. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/765255 · Cited by 2
The best of both worlds: photosynthesis and Solanaceae biodiversity seeking a sustainable food and cosmetic industry
Aguirre-Bottger, C., & Zolla, G. (2024) · Frontiers in Plant Science · doi:10.3389/fpls.2024.1362814 · Cited by 1
Phototropin links blue-light perception with starch accumulation in Chlamydomonas
Yuan, Y. (2022) · theses.fr (ABES) · doi:10.70675/136e01c4z847dz4510z87dfz8ab59dfed96e · Cited by 1
Non-Phosphorylating And Phosphorylating Oxidoreductase Glyceraldehyde-3-Phosphate Dehydrogenase As Part Of A Structure-Based Design In Glycolysis As The Glycolytic Protein G3PD.Preprint
Brenneman, M. R. (2015) · viXra · doi:10.13140/rg.2.1.5122.5048
Premio Mullor. Metabolismo energético y del poder reductor en células autótrofas y heterótrofas
Piattoni, C. V. (2014) · FABICIB · doi:10.14409/fabicib.v17i0.4318
Author to whom all correspondence should be sent
Gomez‐Casati, D. F. (2008)
Self-citation
Comparative analysis of differential gene expression in the culms of sorghum
Ndimande, G. S. (2007) · SUNScholar (Stellenbosch University)
Faculty Opinions recommendation of Nuclear moonlighting of cytosolic glyceraldehyde-3-phosphate dehydrogenase regulates Arabidopsis response to heat stress.
Leister, D., & Kleine, T. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.738312265.793578695
Rising carbon dioxide and nitrogen assimilation impacts the wound-induced hormone response in Arabidopsis thaliana
Tang, L. (2023) · eScholarship@McGill (McGill) · doi:10.82308/4522
REDUCE, REUSE, RECYCLE: EVALUATING THE CONTRIBUTION OF EUTREMA SALSUGINEUM BYPASSES FOR GLYCOLYTIC SUBSTRATE LEVEL PHOSPHORYLATION IN RESPONSE TO LOW PHOSPHATE CONDITIONS
MacLean, M. (2024) · MacSphere (McMaster University) · doi:10.71548/3767
Insight into GABA shunt-associated aldehyde dehydrogenases (ALDH) and stress responses of ALDH superfamily in moss and barleyPreprint
Kopečný, D. J., Bělíček, J., Kopečná, M., Vigouroux, A., Končitíková, R., von Schwartzenberg, K., Supíková, K., Zeljkovıć, S. Ć., Valárik, M., Müller, K., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.13.699213
Antioxidant systems and protein phosphatases in metabolic and signaling responses to oxidative stress
Li, S. (2013) · theses.fr (ABES) · doi:10.70675/ec951085z45bbz421cza81bz05a1bed3d4c9
The Role of nitric oxide in the remodeling of the photosynthetic apparatus under abiotic stress in Chlamydomonas reinhardtii
de Mia, M. (2017) · theses.fr (ABES) · doi:10.70675/518b3c0cz29dfz4585z9afezb5cf881ec110
Functional analysis of catalase mutants and their application to the analysis of NADPH-linked pathways in oxidative signaling in Arabidopsis thaliana
Yang, Z. (2018) · theses.fr (ABES) · doi:10.70675/254c9ffbz7842z4148zbeddz06e38bc460a7
Vers une meilleure compréhension des systèmes antioxydants chez la plante face aux contraintes environnementales : approches expérimentales et modélisation mécaniste
Rahantaniaina, M.-S. (2018) · theses.fr (ABES) · doi:10.70675/e192e680z7502z4434za752z9bb65e3fc85a
Spatiotemporal Dynamics of Cytosolic NADPH in Living Arabidopsis thaliana
Lu, D., Liu, J., Lim, S., Zhong, J. Y., & Lim, B. L. (2026) · Plant Cell & Environment · doi:10.1111/pce.70806

Authors: Rius, S. P., Casati, P., Iglesias, A. A., & Gomez-Casati, D. F.
Affiliations: Consejo Nacional de Investigaciones Científicas y Técnicas (AR)
National University of Rosario (AR)
ORCID: Rius, Sebastián P.
Casati, Paula
Venue: Plant Molecular Biology
Publisher: Springer Science and Business Media LLC
Published: 2006-08
Volume: 61
Issue: 6
Pages: 945-957
ISSN: 0167-4412 (ISSN-L)
1573-5028
DOI: 10.1007/s11103-006-0060-5
OpenAlex: W2075280488
Cited by: 94
References: 49
Citations by year: 2026: 2 · 2025: 4 · 2024: 5 · 2023: 5 · 2022: 2 · 2021: 8 · 2020: 7 · 2019: 5 · 2018: 6 · 2017: 6 · 2016: 5 · 2015: 6 · 2014: 5 · 2013: 6 · 2012: 4
FWCI: 1.22
Type: journal article
Language: en
Open access: green
hdl.handle.net
Licence: cc-by-nc-sa
www.springer.com/tdm (tdm)
Locations: Plant Molecular Biology (publishedVersion)
PubMed (publishedVersion)
CONICET Digital (CONICET) (submittedVersion, cc-by-nc-sa)
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Photosynthetic Processes and Mechanisms
Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant nutrient uptake and metabolism
Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Stress Responses and Tolerance
Keywords: Arabidopsis thaliana mutants, insertion mutants, carbohydrate metabolism, glucose-6-phosphate dehydrogenase, reactive oxygen species, glycolysis, photosynthesis, plant growth and development
MeSH terms: Carbon Dioxide, Chlorophyll, Cytosol, Glycolysis, Microscopy, Fluorescence, Mutation, NADP, Phenotype, Photosynthesis, RNA, Messenger, Superoxides, Gene Expression Regulation, Enzymologic, Mutagenesis, Insertional, Arabidopsis, Reactive Oxygen Species, Gene Expression Regulation, Plant, Gene Expression Regulation, Developmental, Plant Leaves, Reverse Transcriptase Polymerase Chain Reaction, Oligonucleotide Array Sequence Analysis, Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating), Glyceraldehyde 3-Phosphate Dehydrogenase (NADP+)

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

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.

Characterization of an Arabidopsis thaliana mutant lacking a cytosolic non-phosphorylating glyceraldehyde-3-phosphate dehydrogenase

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks

Data sources