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Contribution of the Mevalonate and Methylerythritol Phosphate Pathways to the Biosynthesis of Gibberellins inArabidopsis
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Gibberellins (GAs) are diterpene plant hormones essential for many developmental processes. Although the GA biosynthesis pathway has been well studied, our knowledge on its early stage is still limited. There are two possible routes for the biosynthesis of isoprenoids leading to GAs, the mevalonate (MVA) pathway in the cytosol and the methylerythritol phosphate (MEP) pathway in plastids. To distinguish these possibilities, metabolites from each isoprenoid pathway were selectively labeled with (13)C in Arabidopsis seedlings. Efficient (13)C-labeling was achieved by blocking the endogenous pathway chemically or genetically during the feed of a (13)C-labeled precursor specific to the MVA or MEP pathways. Gas chromatography-mass spectrometry analyses demonstrated that both MVA and MEP pathways can contribute to the biosyntheses of GAs and campesterol, a cytosolic sterol, in Arabidopsis seedlings. While GAs are predominantly synthesized through the MEP pathway, the MVA pathway plays a major role in the biosynthesis of campesterol. Consistent with some crossover between the two pathways, phenotypic defects caused by the block of the MVA and MEP pathways were partially rescued by exogenous application of the MEP and MVA precursors, respectively. We also provide evidence to suggest that the MVA pathway still contributes to GA biosynthesis when this pathway is limiting.
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“In corn, MVA is not the pathway for synthesizing phytosterols; other pathways participate in synthesizing IPP [18,116,143,144].”
From Phytoecdysteroids: Distribution, Structural Diversity, Biosynthesis, Activity, and Crosstalk with Phytohormones (2022) · cites this paper as [143]
Citations
Cites
Biochemistry and molecular biology of plants
Short, T. W. (2001) · Biochemistry and Molecular Biology Education · Cited by 3,833
Biochemistry & molecular biology of plants
(2001) · Choice Reviews Online · doi:10.5860/choice.38-3895 · Cited by 2,980
THE 1-DEOXY-D-XYLULOSE-5-PHOSPHATE PATHWAY OF ISOPRENOID BIOSYNTHESIS IN PLANTS
Lichtenthaler, H. K. (1999) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.50.1.47 · Cited by 1,420
Rohmer, M., & Rohmer, M. (1999) · Natural Product Reports · doi:10.1039/a709175c · Cited by 1,193
Estévez, J. M., Cantero, A., Reindl, A., Reichler, S. A., & León, P. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m100854200 · Cited by 672
Sacchettini, J. C., & Poulter, C. D. (1997) · Science · doi:10.1126/science.277.5333.1788 · Cited by 562
The Arabidopsis GA1 locus encodes the cyclase ent-kaurene synthetase A of gibberellin biosynthesis.
Sun, T., & Kamiya, Y. (1994) · The Plant Cell · doi:10.1105/tpc.6.10.1509 · Cited by 550
Self-citationSilverstone, A. L., Jung, H.-S., Dill, A., Kawaide, H., Kamiya, Y., & Sun, T. (2001) · The Plant Cell · doi:10.1105/tpc.010047 · Cited by 503
Self-citationRohmer, M., Seemann, M., Horbach, S., Bringer-Meyer, S., & Sahm, H. (1996) · Journal of the American Chemical Society · doi:10.1021/ja9538344 · Cited by 484
The deoxyxylulose phosphate pathway of terpenoid biosynthesis in plants and microorganisms
Eisenreich, W., Schwarz, M. K., Cartayrade, A., Arigoni, D., Zenk, M. H., & Bacher, A. (1998) · Chemistry & Biology · doi:10.1016/s1074-5521(98)90002-3 · Cited by 437
Research works printed but not linked: 5
- Hanson, 1969, J. Chem. Soc., 981
- Sun, 1994, Plant Cell, 6, 1509
- Silverstone, 2001, Plant Cell, 13, 1555
- Fujioka, 1997, Plant Cell, 9, 1951
- Choe, 1999, Plant Cell, 11, 207
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Yamaguchi, S. (2008) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.59.032607.092804 · Cited by 2,204
Self-citationThe biosynthesis and nutritional uses of carotenoids
Fraser, P. D. (2003) · Progress in Lipid Research · doi:10.1016/j.plipres.2003.10.002 · Cited by 1,405
Network Analysis of the MVA and MEP Pathways for Isoprenoid Synthesis
Vranová, E., Coman, D., & Gruissem, W. (2013) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-050312-120116 · Cited by 1,168
The role of gibberellin signalling in plant responses to abiotic stress
Colebrook, E. H., Thomas, S. G., Phillips, A. L., & Hedden, P. (2013) · Journal of Experimental Biology · doi:10.1242/jeb.089938 · Cited by 1,085
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Hedden, P., & Thomas, S. G. (2012) · Biochemical Journal · doi:10.1042/bj20120245 · Cited by 938
A Century of Gibberellin Research
Hedden, P., & Sponsel, V. M. (2015) · Journal of Plant Growth Regulation · doi:10.1007/s00344-015-9546-1 · Cited by 613
Yamauchi, Y., Ogawa, M., Kuwahara, A., Hanada, A., Kamiya, Y., & Yamaguchi, S. (2004) · The Plant Cell · doi:10.1105/tpc.018143 · Cited by 579
Self-citationBiogenesis, molecular regulation and function of plant isoprenoids.
Bouvier, F., Rahier, A., & Camara, B. (2005) · Progress in Lipid Research · doi:10.1016/j.plipres.2005.09.003 · Cited by 498
Hemmerlin, A., Hoeffler, J., Meyer, O., Tritsch, D., Kagan, I. A., Grosdemange‐Billiard, C., Rohmer, M., & Bach, T. J. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m302526200 · Cited by 442
The Current Status of Research on Gibberellin Biosynthesis
Hedden, P. (2020) · Plant and Cell Physiology · doi:10.1093/pcp/pcaa092 · Cited by 403
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Wille, A., Zimmermann, P., Vranová, E., Fürholz, A., Laule, O., Bleuler, S., Hennig, L., Prelić, A., von Rohr, P., Thiele, L., et al. (2004) · Genome biology · doi:10.1186/gb-2004-5-11-r92 · Cited by 382
Structure and Dynamics of the Isoprenoid Pathway Network
Vranová, E., Coman, D., & Gruissem, W. (2012) · Molecular Plant · doi:10.1093/mp/sss015 · Cited by 370
A raison d’être for two distinct pathways in the early steps of plant isoprenoid biosynthesis?
Hemmerlin, A., Harwood, J. L., & Bach, T. J. (2011) · Progress in Lipid Research · doi:10.1016/j.plipres.2011.12.001 · Cited by 371
Chemistry of the Retinoid (Visual) Cycle
Kiser, P. D., Golczak, M., & Palczewski, K. (2014) · Chemical Reviews · doi:10.1021/cr400107q · Cited by 353
Tomato as a Source of Carotenoids and Polyphenols Targeted to Cancer Prevention
Martí, R., Roselló, S., & Cebolla‐Cornejo, J. (2016) · Cancers · doi:10.3390/cancers8060058 · Cited by 372
Bömke, C., & Tudzynski, B. (2009) · Phytochemistry · doi:10.1016/j.phytochem.2009.05.020 · Cited by 340
The potential of the mevalonate pathway for enhanced isoprenoid production
Liao, P., Hemmerlin, A., Bach, T. J., & Chye, M. (2016) · Biotechnology Advances · doi:10.1016/j.biotechadv.2016.03.005 · Cited by 336
Enfissi, E. M. A., Fraser, P. D., Lois, L. M., Boronat, A., Schuch, W., & Bramley, P. M. (2004) · Plant Biotechnology Journal · doi:10.1111/j.1467-7652.2004.00091.x · Cited by 329
Carotenoids, versatile components of oxygenic photosynthesis
Domonkos, I., Kis, M., Gombos, Z., & Ughy, B. (2013) · Progress in Lipid Research · doi:10.1016/j.plipres.2013.07.001 · Cited by 310
Phytohormone signaling and crosstalk in regulating drought stress response in plants
Salvi, P., Manna, M., Kaur, H., Thakur, T., Gandass, N., Bhatt, D., & Muthamilarasan, M. (2021) · Plant Cell Reports · doi:10.1007/s00299-021-02683-8 · Cited by 315
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Sun, T. (2008) · The Arabidopsis Book · doi:10.1199/tab.0103 · Cited by 300
Almela, L., Sánchez-Muñoz, B., Fernández-López, J. A., Roca, M. J., & Rabe, V. (2006) · Journal of Chromatography A · doi:10.1016/j.chroma.2006.02.056 · Cited by 271
Glandular trichomes: what comes after expressed sequence tags?
Tissier, A. F. (2012) · The Plant Journal · doi:10.1111/j.1365-313x.2012.04913.x · Cited by 267
Gibberellin biosynthesis and metabolism: A convergent route for plants, fungi and bacteria
Salazar-Cerezo, S., Martínez-Montiel, N., García-Sánchez, J., Pérez-y-Terrón, R., & Martínez-Contreras, R. D. (2018) · Microbiological Research · doi:10.1016/j.micres.2018.01.010 · Cited by 256
Chemistry and Biotechnology of Carotenoids
Namitha, K. K., & Negi, P. S. (2010) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2010.499811 · Cited by 266
Lichtenthaler, H. K. (2007) · Photosynthesis Research · doi:10.1007/s11120-007-9204-y · Cited by 247
Terpene Specialized Metabolism inArabidopsis thaliana
Tholl, D., & Lee, S. (2011) · The Arabidopsis Book · doi:10.1199/tab.0143 · Cited by 253
Rodrı́guez-Concepción, M. (2006) · Phytochemistry Reviews · doi:10.1007/s11101-005-3130-4 · Cited by 244
Rodrı́guez-Concepción, M., Forés, O., Martínez‐García, J. F., González, V. M., Phillips, M. A., Ferrer, A., & Boronat, A. (2003) · The Plant Cell · doi:10.1105/tpc.016204 · Cited by 230
Distinct Isoprenoid Origins of cis- and trans-Zeatin Biosyntheses in Arabidopsis
Kasahara, H., Takei, K., Ueda, N., Hishiyama, S., Yamaya, T., Kamiya, Y., Yamaguchi, S., & Sakakibara, H. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m314195200 · Cited by 232
Self-citationBurlat, V., Oudin, A., Courtois, M., Rideau, M., & St‐Pierre, B. (2004) · The Plant Journal · doi:10.1111/j.1365-313x.2004.02030.x · Cited by 217
Suzuki, M., Kamide, Y., Nagata, N., Seki, H., Ohyama, K., Kato, H., Masuda, K., Sato, S., Kato, T., Tabata, S., et al. (2004) · The Plant Journal · doi:10.1111/j.1365-313x.2004.02003.x · Cited by 203
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Sponsel, V. M., & Hedden, P. (2007) · Springer eBooks · doi:10.1007/978-1-4020-2686-7_4 · Cited by 200
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Hsieh, M., & Goodman, H. M. (2005) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.058735 · Cited by 181
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Flores-Pérez, Ú., Sauret-Gueto, S., Gas‐Pascual, E., Jarvis, P., & Rodrı́guez-Concepción, M. (2008) · The Plant Cell · doi:10.1105/tpc.108.058768 · Cited by 173
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Chow, K. S., Wan, K., Isa, M. N. M., Bahari, A., Tan, S.-H., Harikrishna, K., & Yeang, H.-Y. (2007) · Journal of Experimental Botany · doi:10.1093/jxb/erm093 · Cited by 173
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Towler, M. J., & Weathers, P. J. (2007) · Plant Cell Reports · doi:10.1007/s00299-007-0420-x · Cited by 170
Guevara‐García, A., Román, C. S., Arroyo-Becerra, A., Cortés, M. E., Gutiérrez-Nava, M. D. L. L., & León, P. (2005) · The Plant Cell · doi:10.1105/tpc.104.028860 · Cited by 165
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Xie, Z., Kapteyn, J., & Gang, D. R. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2008.03429.x · Cited by 153
Supply of precursors for carotenoid biosynthesis in plants
Rodrı́guez-Concepción, M. (2010) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2010.06.016 · Cited by 157
Towards efficient terpenoid biosynthesis: manipulating IPP and DMAPP supply
Wang, Q., Quan, S., & Xiao, H. (2019) · Bioresources and Bioprocessing · doi:10.1186/s40643-019-0242-z · Cited by 158
Gutensohn, M., Orlova, I., Nguyen, T. T. H., Davidovich‐Rikanati, R., Ferruzzi, M. G., Sitrit, Y., Lewinsohn, E., Pichersky, E., & Dudareva, N. (2013) · The Plant Journal · doi:10.1111/tpj.12212 · Cited by 146
Córdoba, E., Porta, H., Arroyo-Becerra, A., Roman, C. S., Medina, L., Rodrı́guez-Concepción, M., & León, P. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/erq393 · Cited by 150
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Metabolic routes affecting rubber biosynthesis in Hevea brasiliensis latex
Chow, K.-S., Isa, M. N. M., Bahari, A., Ghazali, A.-K., Alias, H., Mohd.-Zainuddin, Z., Hoh, C.-C., & Wan, K. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/err363 · Cited by 139
Ghirardo, A., Wright, L. P., Bi, Z., Rosenkranz, M., Pulido, P., Rodríguez-Concepción, M., Niinemets, Ü., Brüggemann, N., Gershenzon, J., & Schnitzler, J. (2014) · PLANT PHYSIOLOGY · doi:10.1104/pp.114.236018 · Cited by 139
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Zhu, W., Miao, Q., Sun, D., Yang, G., Wu, C., Huang, J., & Zheng, C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043530 · Cited by 129
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Oudin, A., Mahroug, S., Courdavault, V., Hervouet, N., Zelwer, C., Rodrı́guez-Concepción, M., St‐Pierre, B., & Burlat, V. (2007) · Plant Molecular Biology · doi:10.1007/s11103-007-9190-7 · Cited by 119
Page, J. E., Hause, G., Raschke, M., Gao, W., Schmidt, J., Zenk, M. H., & Kutchan, T. M. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.038133 · Cited by 117
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Kaur, H., Kohli, S. K., Khanna, K., & Bhardwaj, R. (2021) · Physiologia Plantarum · doi:10.1111/ppl.13389 · Cited by 116
Ramos, A., Polle, J. E. W., Tran, D., Cushman, J. C., Jin, E., & Varela, J. C. S. (2011) · ALGAE · doi:10.4490/algae.2011.26.1.003 · Cited by 116
Okada, K., Kasahara, H., Yamaguchi, S., Kawaide, H., Kamiya, Y., Nojiri, H., & Yamane, H. (2008) · Plant and Cell Physiology · doi:10.1093/pcp/pcn032 · Cited by 113
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Yang, D., Du, X., Liang, X., Han, R., Liang, Z., Liu, Y., Liu, F., & Jianjun, Z. (2012) · PLoS ONE · doi:10.1371/journal.pone.0046797 · Cited by 94
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Shih, M.-L., & Morgan, J. A. (2020) · Metabolic Engineering Communications · doi:10.1016/j.mec.2020.e00123 · Cited by 85
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Tarkowská, D., & Strnad, M. (2018) · Planta · doi:10.1007/s00425-018-2878-x · Cited by 87
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Alicandri, E., Paolacci, A. R., Osadolor, S. O., Sorgonà, A., Badiani, M., & Ciaffi, M. (2020) · Journal of Molecular Evolution · doi:10.1007/s00239-020-09930-8 · Cited by 86
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Suzuki, M., Nakagawa, S., Kamide, Y., Kobayashi, K., Ohyama, K., Hashinokuchi, H., Kiuchi, R., Saito, K., Muranaka, T., & Nagata, N. (2009) · Journal of Experimental Botany · doi:10.1093/jxb/erp073 · Cited by 83
Mahroug, S., Burlat, V., & St‐Pierre, B. (2007) · Phytochemistry Reviews · doi:10.1007/s11101-006-9017-1 · Cited by 82
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Jin, H., Song, Z., & Nikolau, B. J. (2012) · The Plant Journal · doi:10.1111/j.1365-313x.2012.04942.x · Cited by 80
Ishiguro, S., Nishimori, Y., Yamada, M., Saito, H., Suzuki, T., Nakagawa, T., Miyake, H., Okada, K., & Nakamura, K. (2010) · Plant and Cell Physiology · doi:10.1093/pcp/pcq068 · Cited by 80
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Upreti, K. K., & Sharma, M. (2016) · Springer eBooks · doi:10.1007/978-81-322-2725-0_2 · Cited by 76
Ohyama, K., Suzuki, M., Masuda, K., Yoshida, S., & Muranaka, T. (2007) · Chemical and Pharmaceutical Bulletin · doi:10.1248/cpb.55.1518 · Cited by 75
Tang, J., Kobayashi, K., Suzuki, M., Matsumoto, S., & Muranaka, T. (2009) · The Plant Journal · doi:10.1111/j.1365-313x.2009.04082.x · Cited by 75
Flores-Pérez, Ú., Pérez-Gil, J., Closa, M., Wright, L. P., Botella‐Pavía, P., Phillips, M. A., Ferrer, A., Gershenzon, J., & Rodrı́guez-Concepción, M. (2009) · Molecular Plant · doi:10.1093/mp/ssp100 · Cited by 74
Xue, L., He, Z., Bi, X., Xu, W. F., Wei, T., Wu, S., & Hu, S. (2019) · BMC Genomics · doi:10.1186/s12864-019-5718-x · Cited by 73
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Suzuki, M., & Muranaka, T. (2006) · Lipids · doi:10.1007/s11745-006-1000-5 · Cited by 71
Otsuka, M., Kenmoku, H., Ogawa, M., Okada, K., Mitsuhashi, W., Sassa, T., Kamiya, Y., Toyomasu, T., & Yamaguchi, S. (2004) · Plant and Cell Physiology · doi:10.1093/pcp/pch149 · Cited by 68
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Metadata
- Authors
- Kasahara, H., Hanada, A., Kuzuyama, T., Takagi, M., Kamiya, Y., & Yamaguchi, S.
- Affiliations
- RIKEN (JP)
- The University of Tokyo (JP)
- Corresponding author
- Yamaguchi, Shinjiro
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 2002-11
- Volume
- 277
- Issue
- 47
- Pages
- 45188-45194
- ISSN
- 0021-9258 (ISSN-L)
- OpenAlex
- W2024426942
- Cited by
- 285
- References
- 45
- Citations by year
- 2026: 12 · 2025: 10 · 2024: 15 · 2023: 6 · 2022: 17 · 2021: 16 · 2020: 13 · 2019: 8 · 2018: 10 · 2017: 10 · 2016: 11 · 2015: 4 · 2014: 10 · 2013: 16 · 2012: 20
- FWCI
- 3.01
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Biological Chemistry (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Plant biochemistry and biosynthesis
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Molecular Biology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Lipid metabolism and biosynthesis
- Keywords
- gibberellin biosynthesis, mevalonate pathway, methylerythritol phosphate pathway, isoprenoid biosynthesis, campesterol, Arabidopsis thaliana, 13C labeling, sterol biosynthesis
- MeSH terms
- Carbon Isotopes, Erythritol, Gibberellins, Lovastatin, Mevalonic Acid, Pentosephosphates, Plant Growth Regulators, Xylulose, Molecular Structure, Arabidopsis, Seedlings
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