The DOI matches its Crossref record; 19 of the 19 references it cites were found in a registry or an index.
A Mitochondrial Pyruvate Carrier Required for Pyruvate Uptake in Yeast, Drosophila , and Humans
Open accessAbstract
Letting Pyruvate In: Transport of pyruvate is an important event in metabolism whereby the pyruvate formed in glycolysis is transported into mitochondria to feed into the tricarboxylic acid cycle (see the Perspective by Murphy and Divakaruni ). Two groups have now identified proteins that are components of the mitochondrial pyruvate transporter. Bricker et al. (p. 96 , published online 24 May) found that the proteins mitochondrial pyruvate carrier 1 and 2 (MPC1 and MPC2) are required for full pyruvate transport in yeast and Drosophila cells and that humans with mutations in MPC1 have metabolic defects consistent with loss of the transporter. Herzig et al. (p. 93 , published online 24 May) identified the same proteins as components of the carrier in yeast. Furthermore, expression of the mouse proteins in bacteria conferred increased transport of pyruvate into bacterial cells.
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.
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?
The cited source says what the claim attributes to it.
In the citing paper
“Pyruvate, the end product of glycolysis, is imported into mitochondria through the mitochondrial pyruvate carrier (MPC) (Bricker et al., 2012; Herzig et al., 2012).”
From Inhibition of the mitochondrial pyruvate carrier in astrocytes reduces amyloid and tau accumulation in the 3xTgAD mouse model of Alzheimer's disease (2024) · cites this paper as Bricker et al., 2012
In the citing paper
“In normoxia, pyruvate is generated via glycolysis and transported across the IMM through the Mitochondrial Pyruvate Carrier (MPC).15,16 Pyruvate is further catabolized inside mitochondria through the TCA cycle.”
From The multifaceted contributions of mitochondria to cellular metabolism (2018) · cites this paper as [16]
In the citing paper
“Pharmacological inhibition of MPC represses mitochondrial pyruvate uptake, shifting reliance to glycolysis for ATP production.”
From The multifaceted contributions of mitochondria to cellular metabolism (2018) · cites this paper as [16]
In the citing paper
“Two recent studies revealed strong evidence that the genes, renamed MPC1 and MPC2, encode the multimeric mitochondrial pyruvate carrier (MPC) complex embedded in the mitochondrial inner mitochondrial membrane (Bricker et al., 2012; Herzig et al., 2012).”
From Regulation of Substrate Utilization by the Mitochondrial Pyruvate Carrier (2014) · cites this paper as Bricker et al., 2012
In the citing paper
“These results are consistent with the severe growth defect previously observed in yeast with deletions in both mpc1 and mitochondrial malic enzyme growing on glucose (Bricker et al., 2012), highlighting the remarkably conserved nature of metabolism across species.”
From Regulation of Substrate Utilization by the Mitochondrial Pyruvate Carrier (2014) · cites this paper as Bricker et al., 2012
In the citing paper
“Our analyses also more explicitly delineate the roles of MPC1 and MPC2 as components of the mitochondrial pyruvate transporter.”
From Regulation of Substrate Utilization by the Mitochondrial Pyruvate Carrier (2014) · cites this paper as Bricker et al., 2012
In the citing paper
“Consistent with this change, Bricker et al. (Bricker et al., 2012) and Herzig et al. (Herzig et al., 2012) both observed growth defects in medium lacking leucine or valine in their characterizations of yeast with Mpc deletions.”
From Regulation of Substrate Utilization by the Mitochondrial Pyruvate Carrier (2014) · cites this paper as Bricker et al., 2012
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
Hallmarks of Cancer: The Next Generation
Hanahan, D., & Weinberg, R. A. (2011) · Cell · doi:10.1016/j.cell.2011.02.013 · Cited by 66,590
Mechanisms linking obesity to insulin resistance and type 2 diabetes
Kahn, S. E., Hull, R. L., & Utzschneider, K. M. (2006) · Nature · doi:10.1038/nature05482 · Cited by 5,448
A Mitochondrial Protein Compendium Elucidates Complex I Disease Biology
Pagliarini, D. J., Calvo, S. E., Chang, B., Sheth, S. A., Vafai, S. B., Ong, S.-E., Walford, G. A., Sugiana, C., Boneh, A., Chen, W. K., et al. (2008) · Cell · doi:10.1016/j.cell.2008.06.016 · Cited by 1,994
The proteome of Saccharomyces cerevisiae mitochondria
Sickmann, A., Reinders, J., Wagner, Y., Joppich, C., Zahedi, R. P., Meyer, H. E., Schönfisch, B., Perschil, I., Chacińska, A., Guiard, B., et al. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2135385100 · Cited by 895
Identification and Functional Expression of the Mitochondrial Pyruvate Carrier
Herzig, S., Raemy, E., Montessuit, S., Veuthey, J.-L., Zamboni, N., Westermann, B., Kunji, E. R. S., & Martinou, J.-C. (2012) · Science · doi:10.1126/science.1218530 · Cited by 747
The mitochondrial pyruvate carrier. Kinetics and specificity for substrates and inhibitors
Halestrap, A. P. (1975) · Biochemical Journal · doi:10.1042/bj1480085 · Cited by 543
Halestrap, A. P., & Denton, R. M. (1974) · Biochemical Journal · doi:10.1042/bj1380313 · Cited by 383
Regulation of the activity of the pyruvate dehydrogenase complex
Harris, R. A., Bowker-Kinley, M. M., Huang, B., & Wu, P. (2002) · Advances in Enzyme Regulation · doi:10.1016/s0065-2571(01)00061-9 · Cited by 313
Identification of the Mitochondrial NAD+ Transporter in Saccharomyces cerevisiae
Todisco, S., Agrimi, G., Castegna, A., & Palmieri, F. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m510425200 · Cited by 228
Halestrap, A. P. (1978) · Biochemical Journal · doi:10.1042/bj1720377 · Cited by 179
Flagged first, then by citations
Cited by
Sorted by citations
Items 301–400 of 844
Paradoxical neuronal hyperexcitability in a mouse model of mitochondrial pyruvate import deficiency
De La Rossa, A., Laporte, M. H., Astori, S., Marissal, T., Montessuit, S., Sheshadri, P., Ramos-Fernández, E., Mendez, P., Khani, A., Quairiaux, C., et al. (2022) · eLife · doi:10.7554/elife.72595 · Cited by 38
Self-citationIdentification and application of keto acids transporters in Yarrowia lipolytica
Guo, H., Liu, P., Madzak, C., Du, G., Zhou, J., & Chen, J. (2015) · Scientific Reports · doi:10.1038/srep08138 · Cited by 39
Choi, J., Koh, E., Lee, Y. S., Lee, H., Kang, H.-G., Yoon, Y. E., Han, W. K., Choi, K. H., & Kim, K. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.04.117 · Cited by 39
Stem Cell Metabolism in Cancer and Healthy Tissues: Pyruvate in the Limelight
Corbet, C. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00958 · Cited by 39
Treating Hepatic Steatosis and Fibrosis by Modulating Mitochondrial Pyruvate Metabolism
McCommis, K. S., & Finck, B. N. (2019) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2018.09.017 · Cited by 39
Timper, K., Paeger, L., Sánchez-Lasheras, C., Varela, L., Jaïs, A., Nolte, H., Vogt, M. C., Hausen, A. C., Heilinger, C., Evers, N., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.09.034 · Cited by 41
Self-citationPendleton, A. L., Antolic, A. T., Kelly, A. C., Davis, M. A., Camacho, L. E., Doubleday, K., Anderson, M. J., Langlais, P. R., Lynch, R. M., & Limesand, S. W. (2020) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00057.2020 · Cited by 39
Mitoribosomal defects aggravate liver cancer via aberrant glycolytic flux and T cell exhaustion
Song, B.-S., Moon, J. S., Tian, J., Lee, H. Y., Sim, B. C., Kim, S., Kang, S., Kim, J. T., Nga, H. T., Benfeitas, R., et al. (2022) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2021-004337 · Cited by 43
Huang, Q., Lou, T., Lü, J., Wang, M., Chen, X., Xue, L., Tang, X., Qi, W., Zhang, Z., Su, H., et al. (2022) · Journal of Ginseng Research · doi:10.1016/j.jgr.2022.02.002 · Cited by 38
Membrane transporters in cell physiology, cancer metabolism and drug response
Alam, S., Doherty, E., Ortega-Prieto, P., Arizanova, J., & Fets, L. (2023) · Disease Models & Mechanisms · doi:10.1242/dmm.050404 · Cited by 44
Tailoring strain construction strategies for muconic acid production in S. cerevisiae and E. coli
Averesch, N. J. H., & Krömer, J. O. (2014) · Metabolic Engineering Communications · doi:10.1016/j.meteno.2014.09.001 · Cited by 38
E4F1-mediated control of pyruvate dehydrogenase activity is essential for skin homeostasis
Goguet-Rubio, P., Seyran, B., Gayte, L., Bernex, F., Sutter, A., Delpech, H., Linares, L. K., Riscal, R., Repond, C., Rodier, G., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1602751113 · Cited by 38
Key features of inhibitor binding to the human mitochondrial pyruvate carrier hetero-dimer
Tavoulari, S., Schirris, T. J. J., Mavridou, V., Thangaratnarajah, C., King, M. S., Jones, D. T. D., Ding, S., Fearnley, I. M., & Kunji, E. R. S. (2022) · Molecular Metabolism · doi:10.1016/j.molmet.2022.101469 · Cited by 38
Wei, P., Bott, A. J., Cluntun, A. A., Morgan, J. T., Cunningham, C. N., Schell, J. C., Ouyang, Y., Ficarro, S. B., Marto, J. A., Danial, N. N., et al. (2022) · Science Advances · doi:10.1126/sciadv.abq0117 · Cited by 39
Self-citationShen, J., Li, C., Wang, M., He, L., Lin, M.-Y., Chen, D.-H., & Zhang, W. (2017) · BMC Plant Biology · doi:10.1186/s12870-017-1175-3 · Cited by 38
Cardiac Metabolism in Perspective
Taegtmeyer, H., Lam, T., & Davogustto, G. (2016) · Comprehensive physiology · doi:10.1002/cphy.c150056 · Cited by 40
Giafaglione, J. M., Crowell, P. D., Delcourt, A. M. L., Hashimoto, T., Ha, S. M., Atmakuri, A., Nunley, N. M., Dang, R. M. A., Tian, M., Diaz, J. A., et al. (2023) · Nature Cell Biology · doi:10.1038/s41556-023-01274-x · Cited by 40
Rauckhorst, A. J., Sheldon, R. D., Pape, D. J., Ahmed, A., Falls-Hubert, K. C., Merrill, R. A., Brown, R. F., Deshmukh, K., Vallim, T., Deja, S., et al. (2024) · Cell Metabolism · doi:10.1016/j.cmet.2024.10.013 · Cited by 40
Self-citationMetabolic control at the cytosol–mitochondria interface in different growth phases of CHO cells
Wahrheit, J., Niklas, J., & Heinzle, E. (2014) · Metabolic Engineering · doi:10.1016/j.ymben.2014.02.001 · Cited by 38
Boeckx, J., Hertog, M., Geeraerd, A. H., & Nicolaï, B. M. (2018) · Postharvest Biology and Technology · doi:10.1016/j.postharvbio.2018.11.017 · Cited by 37
The mitochondrial ADP/ATP carrier exists and functions as a monomer
Kunji, E. R. S., & Ruprecht, J. J. (2020) · Biochemical Society Transactions · doi:10.1042/bst20190933 · Cited by 40
Zhu, K. Y., Zhao, B., Zhang, Y., Kong, J., Rong, L., Liu, S., Wang, Y., Zhang, C., Xiao, D., Foo, J. L., et al. (2022) · ACS Sustainable Chemistry & Engineering · doi:10.1021/acssuschemeng.2c03063 · Cited by 37
Sepsis-induced changes in pyruvate metabolism: insights and potential therapeutic approaches
Nuyttens, L., Vandewalle, J., & Libert, C. (2024) · EMBO Molecular Medicine · doi:10.1038/s44321-024-00155-6 · Cited by 36
MPC1 is essential for PGC-1α-induced mitochondrial respiration and biogenesis
Koh, E., Kim, Y. K., Shin, D., & Kim, K. (2018) · Biochemical Journal · doi:10.1042/bcj20170967 · Cited by 36
Tang, X., Chen, Q., Li, Y., Wang, Y., Zou, H., Fu, W., Niu, Q., Pan, Q., Jiang, P., Xu, X., et al. (2018) · Laboratory Investigation · doi:10.1038/s41374-018-0138-0 · Cited by 36
Park, S.-H., & Hahn, J. (2019) · Scientific Reports · doi:10.1038/s41598-019-40631-5 · Cited by 36
Mitochondrial pyruvate carrier inhibitors improve metabolic parameters in diet-induced obese mice
Hodges, W. T., Jarasvaraparn, C., Ferguson, D., Griffett, K., Gill, L. E., Chen, Y., Ilagan, M. X. G., Hegazy, L., Elgendy, B., Cho, K., et al. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.101554 · Cited by 38
Self-citationTranscriptome Analysis on Key Metabolic Pathways in Rhodotorula mucilaginosa Under Pb(II) Stress
Chen, T., Shi, Y., Peng, C., Tang, L., Chen, Y., Wang, T., Wang, Z., Wang, S., & Li, Z. (2022) · Applied and Environmental Microbiology · doi:10.1128/aem.02215-21 · Cited by 36
Self-citationPioglitazone inhibits mitochondrial pyruvate metabolism and glucose production in hepatocytes
Shannon, C. E., Daniele, G., Galindo, C., Abdul-Ghani, M. A., DeFronzo, R. A., & Norton, L. (2016) · FEBS Journal · doi:10.1111/febs.13992 · Cited by 36
Daverio, Z., Balcerczyk, A., Rautureau, G. J. P., & Panthu, B. (2023) · Cancers · doi:10.3390/cancers15051417 · Cited by 35
Li, Y., He, Y., Zheng, Q., Zhang, J., Pan, X., Zhang, X., Yuan, H., Wang, G., Liu, X., Zhou, X.-L., et al. (2024) · Cell stem cell · doi:10.1016/j.stem.2024.09.015 · Cited by 35
MPC1 deletion is associated with poor prognosis and temozolomide resistance in glioblastoma
Chai, Y., Wang, C., Liu, W., Fan, Y., & Zhang, Y. (2019) · Journal of Neuro-Oncology · doi:10.1007/s11060-019-03226-8 · Cited by 35
Pei, J., Zhang, J., & Cong, Q. (2022) · Bioinformatics · doi:10.1093/bioinformatics/btac527 · Cited by 35
Bölsterli, B. K., Boltshauser, E., Palmieri, L., Spenger, J., Brunner‐Krainz, M., Distelmaier, F., Freisinger, P., Geis, T., Gropman, A. L., Häberle, J., et al. (2022) · Nutrients · doi:10.3390/nu14173605 · Cited by 35
Pyruvate transporter BnaBASS2 impacts seed oil accumulation in Brassica napus
Tang, S., Guo, N., Tang, Q., Peng, F., Liu, Y., Xia, H., Lu, S., & Guo, L. (2022) · Plant Biotechnology Journal · doi:10.1111/pbi.13922 · Cited by 35
Robertson, G. L., Riffle, S., Patel, M., Bodnya, C., Marshall, A. G., Beasley, H. K., Lopez, E. G., Shao, J., Vue, Z., Hinton, A. O., Jr., et al. (2023) · Journal of Cell Science · doi:10.1242/jcs.260370 · Cited by 37
SIRT3 Is a Critical Regulator of Mitochondrial Function of Fibroblasts in Pulmonary Hypertension
Li, M., Plecitá‐Hlavatá, L., Dobrinskikh, E., McKeon, B. A., Gandjeva, A., Riddle, S. R., Laux, A., Prasad, R. R., Kumar, S., Tuder, R. M., et al. (2023) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2022-0360oc · Cited by 35
Seo, S., Kim, J., Lee, J.-W., Nam, O., Chang, K. S., & Jin, E. (2020) · Biotechnology for Biofuels · doi:10.1186/s13068-020-01760-6 · Cited by 34
Quantitative Assessment of Blood Lactate in Shock: Measure of Hypoxia or Beneficial Energy Source
Levitt, D. G., Levitt, J. E., & Levitt, M. D. (2020) · BioMed Research International · doi:10.1155/2020/2608318 · Cited by 38
Development of Novel Mitochondrial Pyruvate Carrier Inhibitors to Treat Hair Loss
Liu, X., Flores, A., Situ, L., Gu, W., Ding, H., Christofk, H. R., Lowry, W. E., & Jung, M. E. (2021) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.0c01570 · Cited by 34
Ablation of mitochondrial DNA results in widespread remodeling of the mitochondrial complexome
Guerrero‐Castillo, S., van Strien, J., Brandt, U., & Arnold, S. (2021) · The EMBO Journal · doi:10.15252/embj.2021108648 · Cited by 34
MPC1 deficiency accelerates lung adenocarcinoma progression through the STAT3 pathway
Zou, H., Chen, Q., Zhang, A., Wang, S., Wu, H., Yuan, Y., Wang, S., Yu, J. H., Luo, M., Wen, X., et al. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-1324-8 · Cited by 34
Ketone bodies for the starving heart
Schulze, P. C., & Wu, J. M. F. (2020) · Nature Metabolism · doi:10.1038/s42255-020-00310-6 · Cited by 34
Mitochondrial pyruvate transport regulates presynaptic metabolism and neurotransmission
Tiwari, A., Myeong, J., Hashemiaghdam, A., Zhang, H., Niu, X., Laramie, M. A., Stunault, M. I., Sponagel, J., Patti, G. J., Shriver, L. P., et al. (2024) · Science Advances · doi:10.1126/sciadv.adp7423 · Cited by 33
Structure of mitochondrial pyruvate carrier and its inhibition mechanism
Zheng, H., Zhang, J., Xu, Y., Fine, E. J., Suomivuori, C., Dror, R. O., & Feng, L. (2025) · Nature · doi:10.1038/s41586-025-08667-y · Cited by 34
Low-frequency stimulation regulates metabolic gene expression in paralyzed muscle
Petrie, M. A., Suneja, M., & Shields, R. K. (2015) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00628.2014 · Cited by 33
Llinares, E., Barry, A. O., & André, B. (2015) · Scientific Reports · doi:10.1038/srep16665 · Cited by 33
Soriano‐Baguet, L., Grusdat, M., Kurniawan, H., Benzarti, M., Binsfeld, C., Ewen, A., Longworth, J., Bonetti, L., Guerra, L., Franchina, D. G., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112153 · Cited by 33
A Mitochondrial Mystery, Solved
Divakaruni, A. S., & Murphy, A. N. (2012) · Science · doi:10.1126/science.1225601 · Cited by 33
Sandoval, I. T., Delacruz, R. G. C., Miller, B. N., Hill, S., Olson, K. A., Gabriel, A. E., Boyd, K. A., Satterfield, C., Remmen, H. V., Rutter, J. P., et al. (2017) · eLife · doi:10.7554/elife.22706 · Cited by 32
Self-citationMetabolic perturbations after pediatric TBI: It's not just about glucose
Bowman, C. E., Scafidi, J., & Scafidi, S. (2019) · Experimental Neurology · doi:10.1016/j.expneurol.2019.03.018 · Cited by 32
Metabolic Roles of Plant Mitochondrial Carriers
Fernie, A. R., Cavalcanti, J. H. F., & Nunes‐Nesi, A. (2020) · Biomolecules · doi:10.3390/biom10071013 · Cited by 36
Xue, C., Li, G., Bao, Z., Zhou, Z., & Lan-juan, L. (2021) · Cancer Cell International · doi:10.1186/s12935-021-01996-8 · Cited by 32
Development of an industrial yeast strain for efficient production of 2,3-butanediol
Huo, G., Foulquié-Moreno, M. R., & Thevelein, J. M. (2022) · Microbial Cell Factories · doi:10.1186/s12934-022-01924-z · Cited by 32
Yiew, N. K. H., Vazquez, J. H., Martino, M. R., Kennon‐McGill, S., Price, J. R., Allard, F. D., Yee, E. U., Layman, A. J., James, L. P., McCommis, K. S., et al. (2023) · Molecular Metabolism · doi:10.1016/j.molmet.2023.101808 · Cited by 32
The role of membrane transport in metabolic engineering of plant primary metabolism
Weber, A. P. M., & Bräutigam, A. (2012) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2012.09.010 · Cited by 32
Reduced Histone Expression or a Defect in Chromatin Assembly Induces Respiration
Galdieri, L. C., Zhang, T., Rogerson, D., & Vančura, A. (2016) · Molecular and Cellular Biology · doi:10.1128/mcb.00770-15 · Cited by 32
Magrì, A., Rosa, M. C. D., Orlandi, I., Guarino, F., Reina, S., Guarnaccia, M., Morello, G., Spampinato, A. G., Cavallaro, S., Messina, A. A., et al. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03342-8 · Cited by 32
Farsani, S. S. M., & Verma, V. (2023) · Frontiers in Oncology · doi:10.3389/fonc.2023.1175532 · Cited by 33
Li, A. M., & Ye, J. (2023) · Annual Review of Cancer Biology · doi:10.1146/annurev-cancerbio-062822-120857 · Cited by 31
Targeting mitochondrial transporters and metabolic reprogramming for disease treatment
Anselme, M., He, H., Lai, C., Luo, W., & Zhong, S. (2025) · Journal of Translational Medicine · doi:10.1186/s12967-025-06976-4 · Cited by 33
Lin, D., Zhang, L., Huang, C., & Shao, W. (2026) · iScience · doi:10.1016/j.isci.2026.115024 · Cited by 35
Immune Cell Metabolism in Systemic Lupus Erythematosus
Choi, S., Titov, A. A., Sivakumar, R., Li, W., & Morel, L. M. (2016) · Current Rheumatology Reports · doi:10.1007/s11926-016-0615-7 · Cited by 32
Metabo-Devo: A metabolic perspective of development
Gándara, L., & Wappner, P. (2018) · Mechanisms of Development · doi:10.1016/j.mod.2018.02.004 · Cited by 31
Oonthonpan, L., Rauckhorst, A. J., Gray, L. R., Boutron, A., & Taylor, E. B. (2019) · JCI Insight · doi:10.1172/jci.insight.126132 · Cited by 31
Self-citationToleco, M. R., Naake, T., Zhang, Y., Heazlewood, J. L., & Fernie, A. R. (2020) · Plants · doi:10.3390/plants9010117 · Cited by 33
Pasqua, T., Rocca, C., Giglio, A., & Angelone, T. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm10040721 · Cited by 31
Eriau, E., Paillet, J., Kroemer, G., & Pol, J. G. (2021) · Cancers · doi:10.3390/cancers13061260 · Cited by 31
Orlandi, I., Pellegrino-Coppola, D., Vai, M., & Dipartimento di Biotecnologie e Bioscienze, U. D. M.-B. (2014) · Microbial Cell · doi:10.15698/mic2014.12.178 · Cited by 32
Lee, C. P., Wirtz, M., & Hell, R. (2013) · Plant and Cell Physiology · doi:10.1093/pcp/pct155 · Cited by 31
Mitochondrial target of thiazolidinediones
Colca, J. R., McDonald, W. G., & Kletzien, R. F. (2014) · Diabetes Obesity and Metabolism · doi:10.1111/dom.12308 · Cited by 32
Multilayered control of peroxisomal activity upon salt stress in S accharomyces cerevisiae
Manzanares‐Estreder, S., Bardisa, J. E., Alarcón, B., Pascual‐Ahuir, A., & Proft, M. (2017) · Molecular Microbiology · doi:10.1111/mmi.13669 · Cited by 31
Methionine supplementation stimulates mitochondrial respiration
Tripodi, F., Castoldi, A., Nicastro, R., Reghellin, V., Lombardi, L., Airoldi, C., Falletta, E., Maffioli, E., Scarcia, P., Palmieri, L., et al. (2018) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2018.09.007 · Cited by 31
Jones, A. E., Li, S., Acevedo, A., Veliova, M., Shirihai, O. S., Stiles, L., & Divakaruni, A. S. (2020) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00235.2020 · Cited by 33
Mitochondrial localization and moderated activity are key to murine erythroid enucleation
Liang, R. H.-S., Menon, V., Qiu, J., Arif, T., Renuse, S., Miao, L., Nowak, R. B., Hartmann, B., Tzavaras, N., Benson, D. L., et al. (2021) · Blood Advances · doi:10.1182/bloodadvances.2021004259 · Cited by 36
Mitochondria in Cancer Energy Metabolism: Culprits or Bystanders?
Kim, A. (2015) · Toxicological Research · doi:10.5487/tr.2015.31.4.323 · Cited by 30
Park, S.-H., Kim, S., & Hahn, J. (2016) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-016-7636-z · Cited by 30
Siripoksup, P., Cao, G., Cluntun, A. A., Maschek, J. A., Pearce, Q., Brothwell, M. J., Jeong, M.-Y., Eshima, H., Ferrara, P. J., Opurum, P. C., et al. (2024) · Journal of Clinical Investigation · doi:10.1172/jci167371 · Cited by 29
Self-citationPetrie, M. A., Suneja, M., Faidley, E. A., & Shields, R. K. (2014) · PLoS ONE · doi:10.1371/journal.pone.0115791 · Cited by 29
Werner, C., Doenst, T., & Schwarzer, M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-802394-5.00004-2 · Cited by 29
Glucose metabolism during in vitro maturation of mouse oocytes: An study using RNA interference
Xie, H., Zhu, S., Zhang, J., Wen, J., Yuan, H., Pan, L., Luo, M., & Tan, J. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.26484 · Cited by 29
Zhou, C., & Fang, J. (2018) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2018.1425671 · Cited by 29
Mitochondrial Metabolism and Aging in Yeast
Baccolo, G., Stamerra, G., Pellegrino-Coppola, D., Orlandi, I., & Vai, M. (2018) · International review of cytology · doi:10.1016/bs.ircmb.2018.05.001 · Cited by 33
Maternal Lipid Metabolism Directs Fetal Liver Programming following Nutrient Stress
Bowman, C. E., Alpergin, E. S. S., Cavagnini, K. S., Smith, D. M., Scafidi, S., & Wolfgang, M. J. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.09.053 · Cited by 29
Mapping mitochondrial respiratory chain deficiencies by respirometry: Beyond the Mito Stress Test
Jaber, S. M., Yadava, N., & Polster, B. M. (2020) · Experimental Neurology · doi:10.1016/j.expneurol.2020.113282 · Cited by 29
Systems Biochemistry Approaches to Defining Mitochondrial Protein Function
Sung, A. Y., Floyd, B. J., & Pagliarini, D. J. (2020) · Cell Metabolism · doi:10.1016/j.cmet.2020.03.011 · Cited by 29
Enhanced Production of Ethyl Lactate in Saccharomyces cerevisiae by Genetic Modification
Ren, J.-Y., Liu, G., Chen, Y., Jiang, S., Ma, Y.-R., Zheng, P., Guo, X.-W., & Xiao, D. (2020) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.0c03967 · Cited by 29
Self-citationBi, G., Bian, Y., Liang, J., Yin, J., Li, R., Zhao, M., Huang, Y., Lu, T., Zhan, C., Fan, H. X., et al. (2021) · Journal of Translational Medicine · doi:10.1186/s12967-021-02889-0 · Cited by 29
Rohatgi, N., Aly, H., Marshall, C. A., McDonald, W. G., Kletzien, R. F., Colca, J. R., & McDaniel, M. L. (2013) · PLoS ONE · doi:10.1371/journal.pone.0062012 · Cited by 30
Proton Transport Chains in Glucose Metabolism: Mind the Proton
Roosterman, D., Meyerhof, W., & Cottrell, G. S. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00404 · Cited by 29
Power2: The power of yeast genetics applied to the powerhouse of the cell
Rutter, J. P., & Hughes, A. L. (2015) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2014.12.002 · Cited by 30
Self-citationNon-bioenergetic roles of mitochondrial GPD2 promote tumor progression
Oh, S., Jo, S., Bajzíková, M., Kim, H. S., Dao, T. T. P., Rohlena, J., Kim, J., Neužil, J., & Park, S. (2022) · Theranostics · doi:10.7150/thno.75973 · Cited by 29
Exogenous pyruvate facilitates cancer cell adaptation to hypoxia by serving as an oxygen surrogate
Yin, C., He, D., Chen, S., Tan, X., & Sang, N. (2016) · Oncotarget · doi:10.18632/oncotarget.10202 · Cited by 28
Fatty acid oxidation alleviates the energy deficiency caused by the loss of MPC1 in MPC1+/− mice
Zou, S., Lang, T., Zhang, B., Huang, K., Gong, L., Luo, H., Xu, W., & He, X. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2017.11.134 · Cited by 28
Petrie, M. A., Sharma, A., Taylor, E. B., Suneja, M., & Shields, R. K. (2019) · Physiological Genomics · doi:10.1152/physiolgenomics.00064.2019 · Cited by 31
Self-citationmiR-26a is Involved in Glycometabolism and Affects Boar Sperm Viability by Targeting PDHX
Wang, W., Liang, K., Chang, Y., Ran, M., Zhang, Y., Ali, M. A., Dai, D., Qazi, I. H., Zhang, M., Zhou, G., et al. (2020) · Cells · doi:10.3390/cells9010146 · Cited by 29
13C MRS and LC–MS Flux Analysis of Tumor Intermediary Metabolism
Shestov, A. A., Lee, S., Nath, K., Guo, L., NELSON, D. S., Roman, J. C., Leeper, D. B., Wasik, M. A., Blair, I. A., & Glickson, J. D. (2016) · Frontiers in Oncology · doi:10.3389/fonc.2016.00135 · Cited by 28
Wang, D., Wang, Q., Yan, G., Qiao, Y., Zhu, B., Liu, B., & Tang, C. (2018) · Molecular Medicine Reports · doi:10.3892/mmr.2018.9079 · Cited by 28
Late-onset caloric restriction alters skeletal muscle metabolism by modulating pyruvate metabolism
Chen, C.-N. (., Lin, S.-Y., Liao, Y.-H., Li, Z.-J., & Wong, A. M.-K. (2015) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00508.2014 · Cited by 27
Fibroblast-to-cardiomyocyte lactate shuttle modulates hypertensive cardiac remodelling
Wei, T., Guo, Y., Huang, C., Sun, M., Zhou, B., Gao, J., & Shen, W. (2023) · Cell & Bioscience · doi:10.1186/s13578-023-01098-0 · Cited by 27
Metadata
- Authors
- Bricker, D. K., Taylor, E. B., Schell, J. C., Orsak, T., Boutron, A., Chen, Y.-C., Cox, J. E., Cardon, C. M., Van Vranken, J. G., Dephoure, N., Redin, C., Boudina, S., Gygi, S. P., Brivet, M., Thummel, C. S., & Rutter, J.
- Affiliations
- University of Utah (US)
- Assistance Publique – Hôpitaux de Paris (FR)
- Department of Biochemistry, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.
- Harvard University (US)
- Institut de génétique et de biologie moléculaire et cellulaire (FR)
- Corresponding author
- Bricker, Daniel K.
- Taylor, Eric B.
- Schell, John C.
- Orsak, Thomas
- Rutter, Jared
- ORCID
- Venue
- Science
- Published
- 2012-07-06
- Volume
- 337
- Issue
- 6090
- Pages
- 96-100
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC3690818
- OpenAlex
- W2019750161
- Cited by
- 843
- References
- 19
- Citations by year
- 2026: 36 · 2025: 60 · 2024: 68 · 2023: 77 · 2022: 70 · 2021: 81 · 2020: 76 · 2019: 58 · 2018: 57 · 2017: 48 · 2016: 52 · 2015: 46 · 2014: 57 · 2013: 38 · 2012: 17
- FWCI
- 20.33
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- HAL (submittedVersion)
- Funders
- National Institutes of Health (2r01dk071962-05a1)
- National Heart, Lung, and Blood Institute (P30HL101310)
- National Institute of General Medical Sciences (R01GM083746, R01GM087346, T32GM007464, R01GM094232)
- National Institute of Diabetes and Digestive and Kidney Diseases (P30DK072437, RC1DK086426, R01 DK-071962, R24DK092784)
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (K99AR059190)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Metabolism and Genetic Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- mitochondrial pyruvate carrier, MPC1, MPC2, pyruvate uptake, pyruvate oxidation, TCA cycle, inner mitochondrial membrane, lactic acidosis, carbon metabolism, yeast, Drosophila, human
- MeSH terms
- Amino Acid Sequence, Amino Acids, Animals, Biological Transport, Citric Acid Cycle, Drosophila melanogaster, Humans, Mitochondria, Molecular Sequence Data, Oxidation-Reduction, Saccharomyces cerevisiae, Point Mutation, Pyruvic Acid, Mitochondrial Proteins, Anion Transport Proteins, Monocarboxylic Acid Transporters, Saccharomyces cerevisiae Proteins, Drosophila Proteins, Mitochondrial Membrane Transport Proteins, Carbohydrate Metabolism, Mitochondrial Membranes, Metabolomics
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