The DOI matches its Crossref record; 62 of the 62 references it cites were found in a registry or an index.
S-nitrosothiols regulate nitric oxide production and storage in plants through the nitrogen assimilation pathway
Open accessAbstract
Nitrogen assimilation plays a vital role in plant metabolism. Assimilation of nitrate, the primary source of nitrogen in soil, is linked to the generation of the redox signal nitric oxide (NO). An important mechanism by which NO regulates plant development and stress responses is through S-nitrosylation, that is, covalent attachment of NO to cysteine residues to form S-nitrosothiols (SNO). Despite the importance of nitrogen assimilation and NO signalling, it remains largely unknown how these pathways are interconnected. Here we show that SNO signalling suppresses both nitrate uptake and reduction by transporters and reductases, respectively, to fine tune nitrate homeostasis. Moreover, NO derived from nitrate assimilation suppresses the redox enzyme S-nitrosoglutathione Reductase 1 (GSNOR1) by S-nitrosylation, preventing scavenging of S-nitrosoglutathione, a major cellular bio-reservoir of NO. Hence, our data demonstrates that (S)NO controls its own generation and scavenging by modulating nitrate assimilation and GSNOR1 activity. Assimilation of nitrate by plant roots leads to the generation of the signalling molecule, nitric oxide. Here Frungillo et al.show that nitric oxide fine-tunes nitrate homeostasis by feedback regulating nitrate transporters and reductases, while also promoting its own storage.
Overview
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
Cites
Statistics
Verification
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.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
Livak, K. J., & Schmittgen, T. D. (2001) · Methods · doi:10.1006/meth.2001.1262 · Cited by 180,860
A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures
Murashige, T., & Skoog, F. (1962) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1962.tb08052.x · Cited by 67,392
Mutation of the mouse klotho gene leads to a syndrome resembling ageing
Kuro-o, M., Matsumura, Y., Aizawa, H., Kawaguchi, H., Suga, T., Utsugi, T., Ohyama, Y., Kurabayashi, M., Kaname, T., Kume, E., et al. (1997) · Nature · doi:10.1038/36285 · Cited by 3,837
Rapid colorimetric determination of nitrate in plant tissue by nitration of salicylic acid
Cataldo, D. A., Maroon, M., Schrader, L. E., & Youngs, V. L. (1975) · Communications in Soil Science and Plant Analysis · doi:10.1080/00103627509366547 · Cited by 3,344
Czechowski, T., Stitt, M., Altmann, T., Udvardi, M. K., & Scheible, W.-R. (2005) · Plant Physiology · doi:10.1104/pp.105.063743 · Cited by 3,203
Biochemistry of nitric oxide and its redox-activated forms
Stamler, J. S., Singel, D. J., & Loscalzo, J. (1992) · Science · doi:10.1126/science.1281928 · Cited by 2,744
Gateway‐compatible vectors for plant functional genomics and proteomics
Earley, K. W., Haag, J. R., Pontes, O., Opper, K., Juehne, T., Song, K., & Pikaard, C. S. (2006) · The Plant Journal · doi:10.1111/j.1365-313x.2005.02617.x · Cited by 1,790
CHL1 Functions as a Nitrate Sensor in Plants
Ho, C.-H., Lin, S.-H., Hu, H.-C., & Tsay, Y.-F. (2009) · Cell · doi:10.1016/j.cell.2009.07.004 · Cited by 1,329
Nitrate: nutrient and signal for plant growth.
Crawford, N. M. (1995) · The Plant Cell · doi:10.1105/tpc.7.7.859 · Cited by 1,010
A metabolic enzyme for S-nitrosothiol conserved from bacteria to humans
Liu, L., Hausladen, A., Zeng, M., Que, L., Heitman, J., & Stamler, J. S. (2001) · Nature · doi:10.1038/35068596 · Cited by 913
Regulation of nitric oxide (NO) production by plant nitrate reductase in vivo and in vitro
Rockel, P., Strube, F., Rockel, A., Wildt, J., & Kaiser, W. M. (2002) · Journal of Experimental Botany · doi:10.1093/jexbot/53.366.103 · Cited by 797
S-nitrosylation of NADPH oxidase regulates cell death in plant immunity
Yun, B.-W., Feechan, A., Yin, M., Saidi, N. B. B., Le Bihan, T., Yu, M., Moore, J. W., Kang, J.-G., Kwon, E., Spoel, S. H., et al. (2011) · Nature · doi:10.1038/nature10427 · Cited by 719
Self-citationDesikan, R., Griffiths, R., Hancock, J., & Neill, S. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.252461999 · Cited by 710
Uptake, allocation and signaling of nitrate
Wang, Y.-Y., Hsu, P.-K., & Tsay, Y.-F. (2012) · Trends in Plant Science · doi:10.1016/j.tplants.2012.04.006 · Cited by 703
Nitrate transporters and peptide transporters
Tsay, Y.-F., Chiu, C.-C., Tsai, C.-B., Ho, C.-H., & Hsu, P.-K. (2007) · FEBS Letters · doi:10.1016/j.febslet.2007.04.047 · Cited by 577
A central role for S-nitrosothiols in plant disease resistance
Feechan, A., Kwon, E., Yun, B.-W., Wang, Y., Pallas, J. A., & Loake, G. J. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0501456102 · Cited by 573
Self-citationNitric Oxide Represses the Arabidopsis Floral Transition
He, Y., Tang, R.-H., Hao, Y., Stevens, R. D., Cook, C. W., Ahn, S. M., Jing, L., Yang, Z., Chen, L., Guo, F., et al. (2004) · Science · doi:10.1126/science.1098837 · Cited by 565
Liu, K.-H., Huang, C.-Y., & Tsay, Y.-F. (1999) · The Plant Cell · doi:10.1105/tpc.11.5.865 · Cited by 536
Nitric oxide in plants: an assessment of the current state of knowledge
Mur, L. A. J., Mandon, J., Persijn, S., Cristescu, S. M., Moshkov, I. E., Novikova, G. V., Hall, M. A., Harren, F. J. M., Hebelstrup, K. H., & Gupta, K. J. (2013) · AoB Plants · doi:10.1093/aobpla/pls052 · Cited by 481
Planchet, E., Jagadis Gupta, K., Sonoda, M., & Kaiser, W. M. (2005) · The Plant Journal · doi:10.1111/j.1365-313x.2005.02335.x · Cited by 439
Nitric Oxide Functions as a Signal in Salt Resistance in the Calluses from Two Ecotypes of Reed
Zhao, L., Zhang, F., Guo, J., Yang, Y., Li, B., & Zhang, L. (2004) · Plant Physiology · doi:10.1104/pp.103.030023 · Cited by 435
Molecular basis of nitrate uptake by the plant nitrate transporter NRT1.1
Parker, J. L., & Newstead, S. (2014) · Nature · doi:10.1038/nature13116 · Cited by 408
An alternative pathway for nitric oxide production in plants: new features of an old enzyme
Yamasaki, H., Sakihama, Y., & Takahashi, S. (1999) · Trends in Plant Science · doi:10.1016/s1360-1385(99)01393-x · Cited by 387
Lee, U., Wie, C., Fernandez, B. O., Feelisch, M., & Vierling, E. (2008) · The Plant Cell · doi:10.1105/tpc.107.052647 · Cited by 372
Kaiser, W. M., & Huber, S. C. (2001) · Journal of Experimental Botany · doi:10.1093/jexbot/52.363.1981 · Cited by 371
From the soil to the seeds: the long journey of nitrate in plants
Dechorgnat, J., Nguyen, C. T., Armengaud, P., Jossier, M., Diatloff, E., Filleur, S., & Daniel‐Vedele, F. (2010) · Journal of Experimental Botany · doi:10.1093/jxb/erq409 · Cited by 369
Dissection of the AtNRT2.1:AtNRT2.2 Inducible High-Affinity Nitrate Transporter Gene Cluster
Li, W., Wang, Y., Okamoto, M., Crawford, N. M., Siddiqi, M. Y., & Glass, A. D. M. (2007) · Plant Physiology · doi:10.1104/pp.106.091223 · Cited by 366
Wilkinson, J. Q., & Crawford, N. M. (1993) · Molecular and General Genetics MGG · doi:10.1007/bf00281630 · Cited by 339
Crystal structure of the plant dual-affinity nitrate transporter NRT1.1
Sun, J., Bankston, J. R., Payandeh, J., Hinds, T. R., Zagotta, W. N., & Zheng, N. (2014) · Nature · doi:10.1038/nature13074 · Cited by 334
Wang, P., Du, Y., Li, Y., Ren, D., & Song, C.-P. (2010) · The Plant Cell · doi:10.1105/tpc.109.072959 · Cited by 312
Fernández-Marcos, M., Sanz, L., Lewis, D. R., Muday, G. K., & Lorenzo, O. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1108644108 · Cited by 303
Detection of protein S-nitrosylation with the biotin-switch technique
Forrester, M. T., Foster, M. W., Benhar, M., & Stamler, J. S. (2009) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2008.09.034 · Cited by 298
Nitric Oxide and Peroxynitrite Interactions with Mitochondria
Radi, R., Cassina, A., & Hodara, R. (2002) · Biological Chemistry · doi:10.1515/bc.2002.044 · Cited by 293
S-Nitrosoglutathione is a substrate for rat alcohol dehydrogenase class III isoenzyme
JENSEN, D. E., BELKA, G. K., & BOIS, G. C. D. (1998) · Biochemical Journal · doi:10.1042/bj3310659 · Cited by 282
Streatfield, S. J., Weber, A., Kinsman, E. A., Häusler, R. E., Li, J., Post-Beittenmiller, D., Kaiser, W. M., Pyke, K. A., Flügge, U.-I., & Chory, J. (1999) · The Plant Cell · doi:10.1105/tpc.11.9.1609 · Cited by 258
Moorhead, G., Douglas, P., Morrice, N., Scarabel, M., Aitken, A., & MacKintosh, C. (1996) · Current Biology · doi:10.1016/s0960-9822(02)70677-5 · Cited by 253
Muños, S., Cazettes, C., Fizames, C., Gaymard, F., Tillard, P., Lepetit, M., Lejay, L., & Gojon, A. (2004) · The Plant Cell · doi:10.1105/tpc.104.024380 · Cited by 235
Modolo, L. V., Augusto, O., Almeida, I. M. G., Magalhaes, J. R., & Salgado, I. (2005) · FEBS Letters · doi:10.1016/j.febslet.2005.05.078 · Cited by 229
Self-citationBent, A. F. (2000) · Plant Physiology · doi:10.1104/pp.124.4.1540 · Cited by 210
Nitric oxide evolution and perception
Neill, S., Bright, J., Desikan, R., Hancock, J., Harrison, J., & Wilson, I. (2007) · Journal of Experimental Botany · doi:10.1093/jxb/erm218 · Cited by 208
The redox switch: dynamic regulation of protein function by cysteine modifications
Spadaro, D., Yun, B., Spoel, S. H., Chu, C., Wang, Y., & Loake, G. J. (2010) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2009.01307.x · Cited by 205
Self-citationRustérucci, C., Espunya, M. C., Díaz, M., Chabannes, M., & Martínez, M. C. (2007) · Plant Physiology · doi:10.1104/pp.106.091686 · Cited by 203
Chen, R., Sun, S., Wang, C., Li, Y., Liang, Y., An, F., Li, C., Dong, H., Yang, X., Zhang, J., et al. (2009) · Cell Research · doi:10.1038/cr.2009.117 · Cited by 187
Redox-based protein modifications: the missing link in plant immune signalling
Spoel, S. H., & Loake, G. J. (2011) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2011.03.007 · Cited by 186
Self-citationNitric oxide-based protein modification: formation and site-specificity of protein S-nitrosylation
Kovacs, I., & Lindermayr, C. (2013) · Frontiers in Plant Science · doi:10.3389/fpls.2013.00137 · Cited by 174
AtGSNOR1 function is required for multiple developmental programs in Arabidopsis
Kwon, E., Feechan, A., Yun, B.-W., Hwang, B.-H., Pallas, J. A., Kang, J.-G., & Loake, G. J. (2012) · Planta · doi:10.1007/s00425-012-1697-8 · Cited by 171
Self-citationModolo, L. V., Augusto, O., Almeida, I. M. G., Pinto-Maglio, C. A. F., Oliveira, H. C., Seligman, K., & Salgado, I. (2006) · Plant Science · doi:10.1016/j.plantsci.2006.02.010 · Cited by 147
Self-citationGupta, K. J., Brotman, Y., Segu, S., Zeier, T. E., Zeier, J., Persijn, S. T., Cristescu, S. M., Harren, F. J. M., Bauwe, H., Fernie, A. R., et al. (2012) · Journal of Experimental Botany · doi:10.1093/jxb/ers348 · Cited by 145
Seligman, K., Saviani, E. E., Oliveira, H. C., Pinto-Maglio, C. A. F., & Salgado, I. (2008) · Plant and Cell Physiology · doi:10.1093/pcp/pcn089 · Cited by 139
Self-citationNitrogen-efficient rice cultivars can reduce nitrate pollution
Hakeem, K. R., Ahmad, A., Iqbal, M., Gücel, S., & Öztürk, M. (2011) · Environmental Science and Pollution Research · doi:10.1007/s11356-010-0434-8 · Cited by 122
A protein microarray-based analysis of S -nitrosylation
Foster, M. W., Forrester, M. T., & Stamler, J. S. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0900729106 · Cited by 114
Enzymology and ecology of the nitrogen cycle
Martínez‐Espinosa, R. M., Cole, J. A., Richardson, D. J., & Watmough, N. J. (2011) · Biochemical Society Transactions · doi:10.1042/bst0390175 · Cited by 106
Crystal structure of a nitrate/nitrite exchanger
Zheng, H., Wisedchaisri, G., & Gonen, T. (2013) · Nature · doi:10.1038/nature12139 · Cited by 99
Structural basis of denitrification
Einsle, O., & Kroneck, P. M. H. (2004) · Biological Chemistry · doi:10.1515/bc.2004.115 · Cited by 98
Yamamoto-Katou, A., Katou, S., Yoshioka, H., Doke, N., & Kawakita, K. (2006) · Plant and Cell Physiology · doi:10.1093/pcp/pcj044 · Cited by 96
Kubienová, L., Kopečný, D., Tylichová, M., Briozzo, P., Skopalová, J., Šebela, M., Navrátil, M., Tâche, R., Luhová, L., Barroso, J. B., et al. (2012) · Biochimie · doi:10.1016/j.biochi.2012.12.009 · Cited by 83
Vitor, S. C., Duarte, G. T., Saviani, E. E., Vincentz, M., Oliveira, H. C., & Salgado, I. (2013) · Planta · doi:10.1007/s00425-013-1906-0 · Cited by 71
Self-citationSalgado, I., Martínez, M. C., Oliveira, H. C., & Frungillo, L. (2013) · Revista Brasileira de Botânica · doi:10.1007/s40415-013-0013-6 · Cited by 55
Self-citationFrungillo, L., de Oliveira, J. F. P., Saviani, E. E., Oliveira, H. C., Martínez, M. C., & Salgado, I. (2012) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2012.11.011 · Cited by 50
Self-citationSkelly, M. J., & Loake, G. J. (2013) · Antioxidants and Redox Signaling · doi:10.1089/ars.2013.5429 · Cited by 34
Self-citationStriking a balance: does nitrate uptake and metabolism regulate both NO generation and scavenging?
Mur, L. A. J., Hebelstrup, K. H., & Gupta, K. J. (2013) · Frontiers in Plant Science · doi:10.3389/fpls.2013.00288 · Cited by 22
Filho, P. R. D. S., Vitor, S. C., Frungillo, L., Saviani, E. E., Oliveira, H. C., & Salgado, I. (2012) · Plant and Cell Physiology · doi:10.1093/pcp/pcs104 · Cited by 21
Self-citation
Cited by
Nitrate Reductase Regulates Plant Nitric Oxide Homeostasis
Chamizo-Ampudia, A., Sanz-Luque, E., Llamas, A., Galvan, A., & Fernandez, E. (2017) · Trends in Plant Science · doi:10.1016/j.tplants.2016.12.001 · Cited by 437
Cassia, R., Nocioni, M., Correa-Aragunde, N., & Lamattina, L. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2018.00273 · Cited by 322
Farnese, F. S., Menezes-Silva, P. E., Gusman, G. S., & Oliveira, J. A. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.00471 · Cited by 316
Metadata
- Authors
- Frungillo, L., Skelly, M. J., Loake, G. J., Spoel, S. H., & Salgado, I.
- Venue
- Nature Communications
- Published
- 2014-11-11
- Volume
- 5
- Issue
- 1
- Pages
- 5401-5401
- ISSN
- 2041-1723 (ISSN-L)
- OpenAlex
- W2150122265
- Cited by
- 256
- References
- 62
- FWCI
- 18.74
- Type
- journal article
- Language
- en
- Open access
- bronze
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.