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Compartmentalization of Mammalian Folate-Mediated One-Carbon Metabolism
Abstract
The recognition that mitochondria participate in folate-mediated one-carbon metabolism grew out of pioneering work beginning in the 1950s from the laboratories of D.M. Greenberg, C.G. Mackenzie, and G. Kikuchi. These studies revealed mitochondria as the site of oxidation of one-carbon donors such as serine, glycine, sarcosine, and dimethylglycine. Subsequent work from these laboratories and others demonstrated the participation of folate coenzymes and folate-dependent enzymes in these mitochondrial processes. Biochemical and molecular genetic approaches in the 1980s and 1990s identified many of the enzymes involved and revealed an interdependence of cytoplasmic and mitochondrial one-carbon metabolism. These studies led to the development of a model of eukaryotic one-carbon metabolism that comprises parallel cytosolic and mitochondrial pathways, connected by one-carbon donors such as serine, glycine, and formate. Sequencing of the human and other mammalian genomes has facilitated identification of the enzymes that participate in this intercompartmental one-carbon metabolism, and animal models are beginning to clarify the roles of the cytoplasmic and mitochondrial isozymes of these enzymes. Identifying the mitochondrial transporters for the one-carbon donors and elucidating how flux through these pathways is controlled are two areas ripe for exploration.
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“The co-factor tetrahydrofolate (THF) is the carrier that mediates 1C transfer reactions for de novo nucleotide synthesis.66,67”
From The multifaceted contributions of mitochondria to cellular metabolism (2018) · cites this paper as [67]
Citations
Cites
The Metabolic and Molecular Bases of Inherited Disease
Scriver, R. C. (1995) · Medical Entomology and Zoology · Cited by 12,101
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
The Wellcome Trust Case Control Consortium, Management Committee, Burton, P. R., Clayton, D. G., Cardon, L. R., Craddock, N., Deloukas, P., Duncanson, A., Kwiatkowski, D. P., McCarthy, M. I., et al. (2007) · Nature · doi:10.1038/nature05911 · Cited by 9,442
The metabolic and molecular bases of inherited disease
Chen, Y.-T. (2001) · Medical Entomology and Zoology · Cited by 6,928
Genomewide Association Analysis of Coronary Artery Disease
Samani, N. J., Erdmann, J., Hall, A. S., Hengstenberg, C., Mangino, M., Mayer, B., Dixon, R. J., Meitinger, T., Braund, P., Wichmann, H.-E., et al. (2007) · New England Journal of Medicine · doi:10.1056/nejmoa072366 · Cited by 2,044
Structure of mitochondrial ADP/ATP carrier in complex with carboxyatractyloside
Pebay‐Peyroula, E., Dahout-Gonzalez, C., Kahn, R., Trézéguet, V., Lauquin, G. J. ‐., & Brandolin, G. (2003) · Nature · doi:10.1038/nature02056 · Cited by 998
The mitochondrial transporter family (SLC25): physiological and pathological implications
Palmieri, F. (2004) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-003-1099-7 · Cited by 764
Wojtczak, L., & Kaniuga, Z. (1966) · Nature · doi:10.1038/2111239a0 · Cited by 691
Chapter 1 Folate‐Mediated One‐Carbon Metabolism
Fox, J. T., & Stover, P. J. (2008) · Vitamins & Hormones · doi:10.1016/s0083-6729(08)00401-9 · Cited by 402
Glycine cleavage system: reaction mechanism, physiological significance, and hyperglycinemia
Kikuchi, G., Motokawa, Y., Yoshida, T., & Hiraga, K. (2008) · Proceedings of the Japan Academy Series B · doi:10.2183/pjab.84.246 · Cited by 381
GENETICS OF SOMATIC MAMMALIAN CELLS
Puck, T. T., & Fisher, H. W. (1956) · The Journal of Experimental Medicine · doi:10.1084/jem.104.3.427 · Cited by 375
Research works printed but not linked: 7
- Barlowe CK, 1988, Biofactors, 1, 171
- Garrow TA, 2001, Homocysteine in Health and Disease, 145
- Kao FT, 1975, Genetics, 79, 343
- Sheid B, 1968, Cancer Res., 28, 2512
- Trippett TM, 2001, Cancer Res., 61, 1941
- Veech RL, 1987, Pyridine Nucleotide Coenzymes. Chemical, Biochemical, and Medical Aspects, Part B, 79
- Wang FK, 1967, Biochem. Z., 346, 458
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BackgroundLiu, J.-J., Liu, S., Gurung, R. L., Lee, J., Zheng, H., Ang, K., Chan, C., Lee, L. S., Han, S. H. Y., Kovalik, J., et al. (2025) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgaf281 · Cited by 3
Jung, A. Y., Botma, A., Lute, C., Blom, H. J., Ueland, P. M., Kvalheim, G., Midttun, Ø., Nagengast, F. M., Steegenga, W. T., & Kampman, E. (2012) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201200069 · Cited by 4
Do, S. K., Choi, S. H., Lee, S. Y., Choi, J. E., Kang, H., Hong, M. J., Kim, J. H., Baek, S. A., Lee, J. H., Lee, W. K., et al. (2020) · Oncology · doi:10.1159/000509658 · Cited by 4
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BackgroundZhang, M., Wang, L., Pei, P., Bao, Y., Guo, J., Wang, L., Chang, S., Xie, X., Cheng, H., Li, Q., et al. (2018) · Analytical Methods · doi:10.1039/c7ay02434g · Cited by 4
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BackgroundBuchler, L. R., Blomgren, L., Bürer, C., Zanotelli, V. R., & Froese, D. S. (2024) · Biochimie · doi:10.1016/j.biochi.2024.11.010 · Cited by 2
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Gao, J., Zou, J., Li, J., Zhang, Y., Qiao, L., Wang, F., Bao, Y., Hu, J., Zhang, T., Xie, Q., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/591768 · Cited by 2
Pavlova, N. N., & Thompson, C. B. (2016) · Wiley eBooks · doi:10.1002/9781119000822.hfcm015 · Cited by 2
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Zhang, D., Ji, A., Yu, R., Jiang, P., Sun, F., & Feng, N. (2025) · 3 Biotech · doi:10.1007/s13205-025-04626-6 · Cited by 1
“In nature, vitamin B 12 is synthesized by microorganisms through de novo synthesis pathways or salvage synthesis pathways, while higher animals and plants cannot synthesize it by themselves.”
The History and Nosology of the Glycine Disorders: A Framework for Clinicians
Selvanathan, A., Hertzog, A., Coughlin, C. R., Swanson, M. A., & Hove, J. L. K. V. (2026) · Journal of Inherited Metabolic Disease · doi:10.1002/jimd.70138 · Cited by 2
Elshoura, Y., Herz, M., Gad, M. Z., & Hanafi, R. S. (2026) · Analytical Chemistry · doi:10.1021/acs.analchem.5c05647 · Cited by 1
Swanson, M. A., Jiang, H., Kolora, L. D., Molino, R., Reisdorph, R. M., Michel, C. R., Doenges, K., Leung, K., Lin, X., Wong, F., et al. (2026) · Journal of Inherited Metabolic Disease · doi:10.1002/jimd.70137 · Cited by 1
“10-Formyltetrahydrofolate is oxidized to carbon dioxide via 10- formyl-tetrahydrofolate dehydrogenase (Aldh1l1 and Aldh1l2) while reducing NADP to NADPH [44, 45], contributing substantially to the reduced NADPH pool in mitochondria [54].”
Shu, Q., Luo, H., Zhong, L., Mo, J., Wei, X., Zhu, Z., Chen, X., She, H., He, F., & Zhu, J. (2026) · Scientific Reports · doi:10.1038/s41598-026-37362-9 · Cited by 1
“Its typical role includes mediating folate-dependent mitochondrial OCM and contributing to the synthesis of formyl methionyl transfer RNA required for protein synthesis initiation 42,43 .”
Long-term metabolic and developmental effects of in vitro embryo technologies in female cattle
Gimeno, I., Berdasco, M., Pato, M. L., Salvetti, P., Carrocera, S., Goyache, F., García, A., Vicente, F., & Gómez, E. (2026) · Journal of Dairy Science · doi:10.3168/jds.2025-26902 · Cited by 1
The Role of One‐Carbon Metabolism in Cancer and Its Therapeutic Significance
Jiang, Y., Zhou, G., Zhang, Q., & Zhou, S. (2026) · MedComm – Oncology · doi:10.1002/mog2.70062 · Cited by 1
Hypoxia-driven microRNA-27b underlies pathologic cardiac endoreplication in heart disease
Mirtschink, P., Yuan, T., Bischof, C., Pham, M. D., Zhu, C., Ware, A. P., Mao, Y., Wu, M., Rogg, E.-M., Bottermann, K., et al. (2026) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-026-02656-x · Cited by 1
“12,35,36 To test this we measured formate and mitochondrial ATP and ADP levels in genetic Hif1 α and miR27b gain-and loss-of-function settings (Fig.”
Mitochondria: from powerhouses of cells to hubs in antitumor immunity
Li, X., Shi, Y., Zhao, Y., Zhu, G., & Jin, L. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1852236 · Cited by 2
Tomé‐Carneiro, J., Cepeda-Vidal, T., Valdés, A., Colás‐Ruiz, N. R., Cruz, E. F., Álvarez, M. B., Matía-Martín, P., & Martínez, J. A. (2026) · European Journal of Nutrition · doi:10.1007/s00394-026-04047-y · Cited by 1
Mathematical modeling of folate-related processes in human placenta
Dotsenko, V. A., & Obolenskaya, M. Y. (2014) · Biopolymers and Cell · doi:10.7124/bc.00088e · Cited by 1
“The most active FDPs are in the cytosol, less active ones – in mitochondria and nucleus [8].”
BackgroundMaternal Nutrition and Cognition
Taylor, R., Smith, R., Collins, C. E., & Hure, A. J. (2017) · Springer eBooks · doi:10.1007/978-3-319-60289-9_3 · Cited by 1
OGT-mediated O-GlcNAcylation on GLDC promotes metastasis in cervical cancer
Cai, P., Jin, X., Zhu, H., Zhu, S., Wang, L., & Jin, J. (2018) · Oncotarget · doi:10.18632/oncotarget.24094 · Cited by 1
“In turn, CH2-THF drives de novo thymidine synthesis and pyrimidine biosynthesis, thus regulating nucleotide synthesis during cell proliferation [8].”
BackgroundMitochondrial dysfunction in kidney diseases
Galvan, D. L., & Perico, L. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819621-2.00005-x · Cited by 1
Cancer Metastasis - Molecular Mechanism and Clinical Therapy
Tutar, Y., & Tutar, L. (2022) · IntechOpen eBooks · doi:10.5772/intechopen.100926 · Cited by 2
Bridging the Gap between tRNA Modifications and the Respiratory Chain
Steiner, R. E., & Ibba, M. (2018) · Biochemistry · doi:10.1021/acs.biochem.8b00377 · Cited by 1
Relationship Between Malignant Brain Tumors and Values of Homocysteine, Folic Acid and Vitamin B12
Djurovic, Z., Mutavdžin, S., Drobnjaković, M., Djurovic, M., Cvrkota, I., & Jovanovic, V. (2019) · EABR. Experimental and Applied Biomedical Research · doi:10.2478/sjecr-2018-0045 · Cited by 1
“Metabolic reactions involving folic acid are called one-carbon metabolic reactions (4).”
BackgroundOccurrence and natural enhancement of folate in oats and barley
Edelmann, M. (2014) · Työväentutkimus Vuosikirja · Cited by 1
DJ1 at the interface between neuro-degeneration and cancer
Meiser, J., Vázquez, A., & Hiller, K. (2017) · Oncotarget · doi:10.18632/oncotarget.14889 · Cited by 1
Assessment of antibiotic resistance in soil and its link to different land use types and intensities
Willms, I. M. (2020) · doi:10.53846/goediss-8102 · Cited by 1
Ravanel, S., & Rébeillé, F. (2012) · Phytonutrients · doi:10.1002/9781118253649.ch6 · Cited by 1
Heyden, K. E., Fiddler, J. L., Xiu, Y., Malysheva, O., Handzlik, M. K., Phinney, W. N., Stiles, L., Stabler, S. P., Metallo, C. M., Caudill, M. A., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.08.29.505750 · Cited by 1
“3B) and was consistent with previous literature (15, 16).”
ResultA serine-folate metabolic unit controls resistance and tolerance of infectionPreprint
Grimes, K., Beckwith, E. J., Pearson, W. H., Jacobson, J., Chaudhari, S., Aughey, G., Larrouy-Maumus, G. J., Southall, T. D., & Dionne, M. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.11.25.517956 · Cited by 1
Morrow, G. P. (2012) · Memorial University Research Repository (Memorial University)
Anderson, D. D., Woeller, C. F., Chiang, E. I., Shane, B., & Stover, P. J. (2012)
Metadata
- Authors
- Tibbetts, A. S., & Appling, D. R.
- Affiliations
- The University of Texas at Austin (US)
- ORCID
- Appling, Dean R.
- Venue
- Annual Review of Nutrition
- Publisher
- Annual Reviews
- Published
- 2010-07-01
- Volume
- 30
- Issue
- 1
- Pages
- 57-81
- ISSN
- 0199-9885 (ISSN-L)
- 1545-4312
- OpenAlex
- W2145912883
- Cited by
- 692
- References
- 157
- Citations by year
- 2026: 42 · 2025: 40 · 2024: 40 · 2023: 53 · 2022: 70 · 2021: 55 · 2020: 61 · 2019: 61 · 2018: 55 · 2017: 33 · 2016: 51 · 2015: 26 · 2014: 33 · 2013: 28 · 2012: 27
- FWCI
- 3.02
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annual Review of Nutrition (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Nursing › Nutrition and Dietetics › Folate and B Vitamins Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Metabolism and Genetic Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Biochemical and Molecular Research
- Keywords
- mitochondrial metabolism, glycine oxidation, folate coenzymes, folate-dependent enzymes, serine, glycine, formate, isozymes, metabolic flux control
- MeSH terms
- Animals, Cell Nucleus, Cytoplasm, Folic Acid, Humans, Mammals, Mitochondria, One-Carbon Group Transferases
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