MitoCarta2.0: an updated inventory of mammalian mitochondrial proteins
Open accessAbstract
Mitochondria are complex organelles that house essential pathways involved in energy metabolism, ion homeostasis, signalling and apoptosis. To understand mitochondrial pathways in health and disease, it is crucial to have an accurate inventory of the organelle's protein components. In 2008, we made substantial progress toward this goal by performing in-depth mass spectrometry of mitochondria from 14 organs, epitope tagging/microscopy and Bayesian integration to assemble MitoCarta (www.broadinstitute.org/pubs/MitoCarta): an inventory of genes encoding mitochondrial-localized proteins and their expression across 14 mouse tissues. Using the same strategy we have now reconstructed this inventory separately for human and for mouse based on (i) improved gene transcript models, (ii) updated literature curation, including results from proteomic analyses of mitochondrial sub-compartments, (iii) improved homology mapping and (iv) updated versions of all seven original data sets. The updated human MitoCarta2.0 consists of 1158 human genes, including 918 genes in the original inventory as well as 240 additional genes. The updated mouse MitoCarta2.0 consists of 1158 genes, including 967 genes in the original inventory plus 191 additional genes. The improved MitoCarta 2.0 inventory provides a molecular framework for system-level analysis of mammalian mitochondria.
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According to the MitoCarta 2.0 database, 654 proteins were specific to or associated with mitochondria.
“According to the MitoCarta 2.0 database [72], 654 proteins were specific to or associated with mitochondria.”
From Neuronal Apolipoprotein E4 Expression Results in Proteome-Wide Alterations and Compromises Bioenergetic Capacity by Disrupting Mitochondrial Function (2019) · cites this paper as [72]
The Introduction and “Human and Mouse MitoCarta2.0” section state that the MitoCarta2.0 inventory contains 1,158 human genes and 1,158 mouse genes encoding mitochondrial proteins, not 654. No page number is available in our copy. (LLM, conf=0.90)
Checked by a reasoning model — may be wrong.
Experimental — accuracy not yet measuredOnly 13 proteins among approximately 1200 proteins of the mitochondrial proteome are encoded by mitochondrial DNA and synthesized inside the organelle.
“However, only 13 proteins among the approximately 1200 proteins from the mitochondrial proteome, are encoded by mitochondrial DNA (mtDNA) and synthesized inside the organelle [34].”
From The connection between the dynamic remodeling of the mitochondrial network and the regulation of muscle mass (2021) · cites this paper as [34]
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BLAST+: architecture and applications
Camacho, C., Coulouris, G., Avagyan, V., Ma, N., Papadopoulos, J., Bealer, K., & Madden, T. L. (2009) · BMC Bioinformatics · doi:10.1186/1471-2105-10-421 · Cited by 22,074 · see citing works
Tissue-based map of the human proteome
Uhlén, M., Fagerberg, L., Hallström, B. M., Lindskog, C., Oksvold, P., Mardinoglu, A., Sivertsson, Å., Kampf, C., Sjöstedt, E., Asplund, A., et al. (2015) · Science · doi:10.1126/science.1260419 · Cited by 15,286 · see citing works
Pfam: the protein families database
Finn, R. D., Bateman, A., Clements, J., Coggill, P., Eberhardt, R. Y., Eddy, S. R., Heger, A., Hetherington, K., Holm, L., Mistry, J., et al. (2014) · Nucleic Acids Research · doi:10.1093/nar/gkt1223 · Cited by 6,148 · see citing works
UniProt: a hub for protein information
The UniProt Consortium (2015) · Nucleic Acids Research · doi:10.1093/nar/gku989 · Cited by 5,106 · see citing works
Predicting subcellular localization of proteins based on their N-terminal amino acid sequence.
Emanuelsson, O., Nielsen, H., Brunak, S., & von Heijne, G. (2000) · Journal of Molecular Biology · doi:10.1006/jmbi.2000.3903 · Cited by 4,419 · see citing works
A gene atlas of the mouse and human protein-encoding transcriptomes
Su, A. I., Wiltshire, T., Batalov, S., Lapp, H., Ching, K. A., Block, D., Zhang, J., Soden, R., Hayakawa, M., Kreiman, G., et al. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0400782101 · Cited by 3,475 · see citing works
Entrez Gene: gene-centered information at NCBI
Maglott, D. R., Ostell, J., Pruitt, K. D., & Tatusova, T. A. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq1237 · Cited by 2,117 · see citing works
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 · see citing works
Self-citationIntegrative genomics identifies MCU as an essential component of the mitochondrial calcium uniporter
Baughman, J. M., Perocchi, F., Girgis, H. S., Plovanich, M. E., Belcher-Timme, C. A., Sancak, Y., Bao, X., Strittmatter, L., Goldberger, O., Bogorad, R., et al. (2011) · Nature · doi:10.1038/nature10234 · Cited by 1,926 · see citing works
Self-citationThe genome sequence of Rickettsia prowazekii and the origin of mitochondria
Andersson, S. G. E., Zomorodipour, A., Andersson, J. O., Sicheritz-Pontén, T., Alsmark, U. C. M., Podowski, R. M., Näslund, A. K., Eriksson, A.-S., Winkler, H. H., & Kurland, C. G. (1998) · Nature · doi:10.1038/24094 · Cited by 1,697 · see citing works
Proteomic Mapping of Mitochondria in Living Cells via Spatially Restricted Enzymatic Tagging
Martell, J. D., Ting, A. Y., Rhee, H., Zou, P., Udeshi, N. D., Mootha, V. K., & Carr, S. A. (2012) · DSpace@MIT (Massachusetts Institute of Technology) · Cited by 1,330 · see citing works
Self-citationNCBI Reference Sequences (RefSeq): current status, new features and genome annotation policy
Pruitt, K. D., Tatusova, T., Brown, G. R., & Maglott, D. R. (2012) · Nucleic Acids Research · doi:10.1093/nar/gkr1079 · Cited by 1,149 · cited 1× · see citing works
“0 database is based on human and mouse RefSeq proteins (release 63) (16) that are mapped to NCBI Gene loci (ftp.”
BackgroundThe Universal Protein Resource (UniProt): an expanding universe of protein information
Wu, C. H. (2005) · Nucleic Acids Research · doi:10.1093/nar/gkj161 · Cited by 1,116 · see citing works
Finn, R. D., Clements, J., Arndt, W. D., Miller, B. L., Wheeler, T. J., Schreiber, F., Bateman, A. G., & Eddy, S. R. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv397 · Cited by 911 · see citing works
MICU1 encodes a mitochondrial EF hand protein required for Ca2+ uptake
Perocchi, F., Gohil, V. M., Girgis, H. S., Bao, X. R., McCombs, J. E., Palmer, A. E., & Mootha, V. K. (2010) · Nature · doi:10.1038/nature09358 · Cited by 881 · see citing works
Self-citationGene: a gene-centered information resource at NCBI
Brown, G., Hem, V., Katz, K., Ovetsky, M., Wallin, C., Ermolaeva, O. D., Tolstoy, I., Tatusova, T. A., Pruitt, K. D., Maglott, D. R., et al. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku1055 · Cited by 706 · see citing works
Mootha, V. K., Handschin, C., Arlow, D., Xie, X., St. Pierre, J., Sihag, S., Yang, W., Altshuler, D., Puigserver, P., Patterson, N., et al. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0401401101 · Cited by 688 · see citing works
Self-citationCOMPARTMENTS: unification and visualization of protein subcellular localization evidence
Binder, J. X., Pletscher-Frankild, S., Tsafou, K., Stolte, C., O’Donoghue, S. I., Schneider, R., & Jensen, L. J. (2014) · Database · doi:10.1093/database/bau012 · Cited by 649 · see citing works
Entrez Gene: gene-centered information at NCBI
Maglott, D., Ostell, J., Pruitt, K. D., & Tatusova, T. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkl993 · Cited by 633 · see citing works
The Mitochondrial Proteome and Human Disease
Calvo, S. E., & Mootha, V. K. (2010) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-082509-141720 · Cited by 590 · see citing works
Self-citationmtDNA Variation and Analysis Using Mitomap and Mitomaster
Lott, M. T., Leipzig, J. N., Derbeneva, O. A., Xie, H. M., Chalkia, D., Sarmady, M., Procaccio, V., & Wallace, D. C. (2013) · Current Protocols in Bioinformatics · doi:10.1002/0471250953.bi0123s44 · Cited by 557 · see citing works
MITOMAP: a human mitochondrial genome database
Kogelnik, A. M. (1996) · Nucleic Acids Research · doi:10.1093/nar/24.1.177 · Cited by 524 · see citing works
Hung, V., Zou, P., Rhee, H.-W., Udeshi, N. D., Cracan, V., Svinkina, T., Carr, S. A., Mootha, V. K., & Ting, A. Y. (2014) · Molecular Cell · doi:10.1016/j.molcel.2014.06.003 · Cited by 517 · see citing works
Self-citationMinimum birth prevalence of mitochondrial respiratory chain disorders in children
Skladal, D. (2003) · Brain · doi:10.1093/brain/awg170 · Cited by 487 · see citing works
Molecular Diagnosis of Infantile Mitochondrial Disease with Targeted Next-Generation Sequencing
Calvo, S. E., Compton, A. G., Hershman, S. G., Lim, S. C., Lieber, D. S., Tucker, E. J., Laskowski, A., Garone, C., Liu, S., Jaffe, D. B., et al. (2012) · Science Translational Medicine · doi:10.1126/scitranslmed.3003310 · Cited by 476 · see citing works
Self-citationExpression analysis of G Protein-Coupled Receptors in mouse macrophages
Lattin, J. E., Schroder, K., Su, A. I., Walker, J. R., Zhang, J., Wiltshire, T., Saijo, K., Glass, C. K., Hume, D. A., Kellie, S., et al. (2008) · Immunome Research · doi:10.1186/1745-7580-4-5 · Cited by 439 · see citing works
Calvo, S. E., Tucker, E. J., Compton, A. G., Kirby, D. M., Crawford, G., Burtt, N. P., Rivas, M. A., Guiducci, C., Bruno, D. L., Goldberger, O., et al. (2010) · Nature Genetics · doi:10.1038/ng.659 · Cited by 362 · see citing works
Self-citationSystematic identification of human mitochondrial disease genes through integrative genomics
Calvo, S. E., Jain, M., Xie, X. S., Sheth, S. A., Chang, B., Goldberger, O., Spinazzola, A., Zeviani, M., Carr, S. A., & Mootha, V. K. (2006) · Nature Genetics · doi:10.1038/ng1776 · Cited by 344 · see citing works
Self-citationDiscovery of Genes Essential for Heme Biosynthesis through Large-Scale Gene Expression Analysis
Nilsson, R., Schultz, I. J., Pierce, E. L., Soltis, K. A., Naranuntarat, A., Ward, D. M., Baughman, J. M., Paradkar, P. N., Kingsley, P. D., Culotta, V., et al. (2009) · Cell Metabolism · doi:10.1016/j.cmet.2009.06.012 · Cited by 213 · see citing works
Self-citationTargeted exome sequencing of suspected mitochondrial disorders
Lieber, D. S., Calvo, S. E., Shanahan, K., Slate, N. G., Liu, S., Hershman, S. G., Gold, N. B., Chapman, B., Thorburn, D. R., Berry, G. T., et al. (2013) · Neurology · doi:10.1212/wnl.0b013e3182918c40 · Cited by 188 · see citing works
Self-citationMitoProteome: mitochondrial protein sequence database and annotation system
Cotter, D. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkh048 · Cited by 175 · see citing works
MitoP2: the mitochondrial proteome database--now including mouse data
Prokisch, H. (2005) · Nucleic Acids Research · doi:10.1093/nar/gkj127 · Cited by 95 · see citing works
Lanning, N. J., Looyenga, B. D., Kauffman, A. L., Niemi, N. M., Sudderth, J., DeBerardinis, R. J., & MacKeigan, J. P. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.03.065 · Cited by 94 · see citing works
MitoMiner: a data warehouse for mitochondrial proteomics data
Smith, A. C., Blackshaw, J., & Robinson, A. J. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkr1101 · Cited by 90 · see citing works
Chapter 1 The Mitochondrial Proteome Database
Elstner, M., Andréoli, C., Klopstock, T., Meitinger, T., & Prokisch, H. (2009) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(09)05001-0 · Cited by 85 · see citing works
MitoP2, an integrated database on mitochondrial proteins in yeast and man
Andréoli, C. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkh137 · Cited by 83 · see citing works
Proteomic Mapping of Mitochondria in Living Cells via Spatially Restricted Enzymatic Tagging
Rhee, H.-W., Zou, P., Udeshi, N. D., Martell, J. D., Mootha, V. K., Carr, S. A., & Ting, A. Y. (2013) · Science · doi:10.1126/science.1230593 · Cited by 83 · see citing works
Self-citationMitoMiner, an Integrated Database for the Storage and Analysis of Mitochondrial Proteomics Data
Smith, A. C., & Robinson, A. J. (2009) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m800373-mcp200 · Cited by 76 · see citing works
MitoP2: An Integrative Tool for the Analysis of the Mitochondrial Proteome
Elstner, M., Andréoli, C., Ahting, U., Tetko, I. V., Klopstock, T., Meitinger, T., & Prokisch, H. (2008) · Molecular Biotechnology · doi:10.1007/s12033-008-9100-5 · Cited by 70 · see citing works
Saccharomycesgenome database provides new regulation data
Costanzo, M. C., Engel, S. R., Wong, E. D., et al. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt1158 · Cited by 60 · see citing works
Falk, M. J., Pierce, E. A., Consugar, M. B., Xie, H. M., Guadalupe, M., Hardy, O., Rappaport, E. F., Wallace, D. C., LeProust, E. M., & Gai, X. (2012) · PubMed · Cited by 56 · see citing works
Background correction using dinucleotide affinities improves the performance of GCRMA
Gharaibeh, R. Z., Fodor, A. A., & Gibas, C. (2008) · BMC Bioinformatics · doi:10.1186/1471-2105-9-452 · Cited by 46 · see citing works
Regulators of membrane trafficking andMycobacterium tuberculosis phagosome maturation block
Fratti, R. A., Vergne, I., Chua, J., Skidmore, J. M., & Deretic, V. P. (2000) · Electrophoresis · doi:10.1002/1522-2683(20001001)21:16 · Cited by 43 · see citing works
CLYBL is a polymorphic human enzyme with malate synthase and β-methylmalate synthase activity
Strittmatter, L., Li, Y., Nakatsuka, N. J., et al. (2013) · Human Molecular Genetics · doi:10.1093/hmg/ddt624 · Cited by 41 · see citing works
Mitoproteome: Human Heart Mitochondrial Protein Sequence Database
Guda, P., Subramaniam, S., & Guda, C. (2006) · Humana Press eBooks · doi:10.1385/1-59745-214-9:375 · Cited by 12 · see citing works
MitoP2, an Integrated Database for Mitochondrial Proteins
Prokisch, H., & Ahting, U. (2007) · Methods in molecular biology · doi:10.1007/978-1-59745-365-3_39 · Cited by 10 · see citing works
Flagged first, then by citations
Research works printed but not linked: 1
- [15]Calvo S. Jain M. Xie X. Sheth S.A. Chang B. Goldberger O.A. Spinazzola A. Zeviani M. Carr S.A. Mootha V.K. Systematic identification of human mitochondrial disease genes through integrative genomics Nat. Genet. 2006 38 576 582 16582907
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Efficient proximity labeling in living cells and organisms with TurboID
Branon, T. C., Bosch, J. A., Sanchez, A. D., Udeshi, N. D., Svinkina, T., Carr, S. A., Feldman, J. L., Perrimon, N., & Ting, A. Y. (2018) · Nature Biotechnology · doi:10.1038/nbt.4201 · Cited by 2,174 · see citing works
The multifaceted contributions of mitochondria to cellular metabolism
Spinelli, J. B., & Haigis, M. C. (2018) · Nature Cell Biology · doi:10.1038/s41556-018-0124-1 · Cited by 1,935 · see citing works
Conserved cell types with divergent features in human versus mouse cortex
Hodge, R. D., Bakken, T. E., Miller, J. A., Smith, K. A., Barkan, E. R., Graybuck, L. T., Close, J. L., Long, B., Johansen, N., Penn, O., et al. (2019) · Nature · doi:10.1038/s41586-019-1506-7 · Cited by 1,775 · see citing works
The Science and Translation of Lactate Shuttle Theory
Brooks, G. A. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2018.03.008 · Cited by 1,486 · see citing works
SynGO: An Evidence-Based, Expert-Curated Knowledge Base for the Synapse
Koopmans, F., van Nierop, P., Andres-Alonso, M., Byrnes, A., Cijsouw, T., Coba, M. P., Cornelisse, L. N., Farrell, R. J., Goldschmidt, H. L., Howrigan, D. P., et al. (2019) · Neuron · doi:10.1016/j.neuron.2019.05.002 · Cited by 938 · see citing works
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome
Huttlin, E. L., Bruckner, R. J., Navarrete-Perea, J., Cannon, J. R., Baltier, K., Gebreab, F., Gygi, M. P., Thornock, A., Zarraga, G., Tam, S., et al. (2020) · doi:10.1101/2020.01.19.905109 · Cited by 960 · see citing works
Quirós, P. M., Prado, M. A., Zamboni, N., D’Amico, D., Williams, R. W., Finley, D., Gygi, S. P., & Auwerx, J. (2017) · Journal of Cell Biology · doi:10.1083/jcb.201702058 · Cited by 832 · see citing works
Glutamine Metabolism in Cancer: Understanding the Heterogeneity
Cluntun, A. A., Lukey, M. J., Cerione, R. A., & Locasale, J. W. (2017) · Trends in Cancer · doi:10.1016/j.trecan.2017.01.005 · Cited by 796 · see citing works
Lactate as a fulcrum of metabolism
Brooks, G. A. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101454 · Cited by 724 · see citing works
Vitamin B <sub>3</sub> modulates mitochondrial vulnerability and prevents glaucoma in aged mice
Williams, P. A., Harder, J. M., Foxworth, N. E., Cochran, K. E., Philip, V. M., Porciatti, V., Smithies, O., & John, S. W. M. (2017) · Science · doi:10.1126/science.aal0092 · Cited by 617 · see citing works
Genetic identification of brain cell types underlying schizophrenia
Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Skene, N. G., Bryois, J., Bakken, T. E., Breen, G., Crowley, J. J., Gaspar, H. A., Giusti-Rodriguez, P., Hodge, R. D., Miller, J. A., et al. (2018) · Nature Genetics · doi:10.1038/s41588-018-0129-5 · Cited by 651 · see citing works
Endoplasmic reticulum-mitochondrial contactology: structure and signaling functions
Csordás, G., Weaver, D., & Hajnóczky, G. (2018) · Trends in Cell Biology · doi:10.1016/j.tcb.2018.02.009 · Cited by 625 · see citing works
Maintenance of Skeletal Muscle Mitochondria in Health, Exercise, and Aging
Hood, D. A., Memme, J. M., Oliveira, A. N., & Triolo, M. (2019) · Annual Review of Physiology · doi:10.1146/annurev-physiol-020518-114310 · Cited by 567 · see citing works
Mitochondrial quality control and muscle mass maintenance.
Romanello, V., & Sandri, M. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2015.00422 · Cited by 434 · see citing works
da Silveira, W. A., Fazelinia, H., Rosenthal, S. B., Laiakis, E. C., Kim, M. S., Meydan, C., Kidane, Y., Rathi, K. S., Smith, S. M., Stear, B., et al. (2020) · Cell · doi:10.1016/j.cell.2020.11.002 · Cited by 402 · see citing works
“The mitochondrial genes were obtained from MitoCarta.”
InfluentialTan, H., Yang, K., Li, Y., Shaw, T. I., Wang, Y., Blanco, D. B., Wang, X., Cho, J.-H., Wang, H., Rankin, S., et al. (2017) · Immunity · doi:10.1016/j.immuni.2017.02.010 · Cited by 372 · see citing works
What Is Nuclear Factor Kappa B (NF-κB) Doing in and to the Mitochondrion?
Albensi, B. C. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00154 · Cited by 341 · see citing works
Exercise and mitochondrial health
Memme, J. M., Erlich, A. T., Phukan, G., & Hood, D. A. (2021) · The Journal of Physiology · doi:10.1113/jp278853 · Cited by 343 · see citing works
Mapping the Genetic Landscape of Human Cells
Horlbeck, M. A., Xu, A., Wang, M., Bennett, N. K., Park, C. Y., Bogdanoff, D., Adamson, B., Chow, E. D., Kampmann, M., Peterson, T. R., et al. (2018) · Cell · doi:10.1016/j.cell.2018.06.010 · Cited by 319 · see citing works
Human neocortical expansion involves glutamatergic neuron diversification
Berg, J., Sorensen, S. A., Ting, J. T., Miller, J. A., Chartrand, T., Buchin, A., Bakken, T. E., Budzillo, A., Dee, N., Ding, S.-L., et al. (2021) · Nature · doi:10.1038/s41586-021-03813-8 · Cited by 285 · see citing works
A Class of Reactive Acyl-CoA Species Reveals the Non-enzymatic Origins of Protein Acylation
Wagner, G. R., Bhatt, D. P., O’Connell, T. M., Thompson, J. W., Dubois, L. G., Backos, D. S., Yang, H., Mitchell, G. A., Ilkayeva, O. R., Stevens, R. D., et al. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.03.006 · Cited by 258 · see citing works
The epigenetic landscape related to reactive oxygen species formation in the cardiovascular system
Kietzmann, T., Petry, A., Shvetsova, A., Gerhold, J. M., & Görlach, A. (2017) · British Journal of Pharmacology · doi:10.1111/bph.13792 · Cited by 253 · see citing works
Jamwal, S., Blackburn, J. K., & Elsworth, J. D. (2021) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2020.107705 · Cited by 236 · see citing works
Grassi, D., Howard, S., Zhou, M., Diaz-Perez, N., Urban, N. T., Guerrero-Given, D., Kamasawa, N., Volpicelli-Daley, L. A., LoGrasso, P., & Lasmézas, C. I. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1713849115 · Cited by 228 · see citing works
The ADP/ATP translocase drives mitophagy independent of nucleotide exchange
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Romanello, V., & Sandri, M. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03662-0 · Cited by 197 · see citing works
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Mapping spatial transcriptome with light-activated proximity-dependent RNA labeling
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Nicotinamide adenine dinucleotide is transported into mammalian mitochondria
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Kim, Y., Zheng, X., Ansari, Z., Bunnell, M. C., Herdy, J. R., Traxler, L., Lee, H., Paquola, A. C. M., Blithikioti, C., Ku, M., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.04.105 · Cited by 117 · see citing works
Orr, A. L., Kim, C., Jimenez-Morales, D., Newton, B. W., Johnson, J. R., Krogan, N. J., Swaney, D. L., & Mahley, R. W. (2019) · Journal of Alzheimer's Disease · doi:10.3233/jad-181184 · Cited by 103 · see citing works
Granata, C., Caruana, N. J., Botella, J., Jamnick, N. A., Huynh, K., Kuang, J., Janssen, H. A., Reljic, B., Mellett, N. A., Laskowski, A., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-27153-3 · Cited by 93 · see citing works
Xu, Z., Fu, T., Guo, Q., Zhou, D., Sun, W., Zhou, Z., Chen, X., Zhang, J., Liu, L., Xiao, L., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-28557-5 · Cited by 82 · see citing works
Mapping the multiscale structure of biological systems
Schaffer, L. V., & Ideker, T. (2021) · Cell Systems · doi:10.1016/j.cels.2021.05.012 · Cited by 75 · see citing works
Sensing the Stress: A Role for the UPRmt and UPRam in the Quality Control of Mitochondria
Callegari, S., & Dennerlein, S. (2018) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2018.00031 · Cited by 58 · see citing works
Vincow, E. S., Thomas, R. E., Merrihew, G. E., Shulman, N. J., Bammler, T. K., MacDonald, J. W., MacCoss, M. J., & Pallanck, L. J. (2019) · Autophagy · doi:10.1080/15548627.2019.1586258 · Cited by 54 · see citing works
Milev, M. P., Saint‐Dic, D., Zardoui, K., Klopstock, T., Law, C., Distelmaier, F., & Sacher, M. (2021) · Journal of Inherited Metabolic Disease · doi:10.1002/jimd.12312 · Cited by 53 · see citing works
Stefanova, N. A., Ershov, N. I., & Kolosova, N. G. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/3984906 · Cited by 40 · see citing works
Exercise is muscle mitochondrial medicine
Oliveira, A. N., Richards, B. J., Slavin, M., & Hood, D. A. (2021) · Exercise and Sport Sciences Reviews · doi:10.1249/jes.0000000000000250 · Cited by 26 · see citing works
Weight loss increases skeletal muscle mitochondrial energy efficiency in obese mice
Ferrara, P. J., Lang, M. J., Johnson, J. M., Watanabe, S., McLaughlin, K. L., Alan Maschek, J., Verkerke, A. R. P., Siripoksup, P., Chaix, A., Cox, J. E., et al. (2023) · Life Metabolism · doi:10.1093/lifemeta/load014 · Cited by 26 · see citing works
Noel, B. M., Ouellette, S. B., Marholz, L., Dickey, D., Navis, C., Yang, T.-Y., Nguyen, V., Parker, S. J., Bernlohr, D., Sachs, Z., et al. (2019) · Journal of Proteome Research · doi:10.1021/acs.jproteome.9b00028 · Cited by 24 · see citing works
Preston, C. C., Larsen, T. D., Eclov, J. A., Louwagie, E. J., Gandy, T. C. T., Faustino, R. S., & Baack, M. L. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.570846 · Cited by 22 · see citing works
Liu, X., Zhang, Y., Ward, L. D., Yan, Q., Bohnuud, T., Hernandez, R., Lao, S., Yuan, J., & Fan, F. (2021) · Scientific Reports · doi:10.1038/s41598-021-95354-3 · Cited by 21 · see citing works
Dasari, S., Newsom, S. A., Ehrlicher, S. E., Stierwalt, H. D., & Robinson, M. M. (2018) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00051.2018 · Cited by 21 · see citing works
Not aging but calorie restriction strongly affects protein oxidation in heart and brain mitochondria
Fan, S., Ramallo‐Guevara, C., Frenzel, M., Yanai, S., Goto, S., Sugawa, M. D., Dencher, N. A., & Poetsch, A. (2026) · Aging Cell · doi:10.1111/acel.70339 · Cited by 1 · see citing works
- Authors
- Calvo, S. E., Clauser, K. R., & Mootha, V. K.
- Affiliations
- Broad Institute (US)
- Corresponding author
- Mootha, Vamsi K.
- Venue
- Nucleic Acids Research
- Publisher
- Oxford University Press (OUP)
- Published
- 2015-10-07
- Volume
- 44
- Issue
- D1
- Pages
- D1251-D1257
- ISSN
- 0305-1048 (ISSN-L)
- 1362-4962
- PMC
- PMC4702768
- OpenAlex
- W2180760460
- Cited by
- 1,251
- References
- 46
- Citations by year
- 2026: 40 · 2025: 54 · 2024: 56 · 2023: 70 · 2022: 115 · 2021: 186 · 2020: 218 · 2019: 177 · 2018: 161 · 2017: 108 · 2016: 64 · 2015: 2
- FWCI
- 48.46
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Nucleic Acids Research (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Digital Access to Scholarship at Harvard (DASH) (Harvard University) (submittedVersion, cc-by)
- HighWire Press Open Archive (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- National Institutes of Health (GM0077465)
- National Institute of General Medical Sciences (GM0077465, R01GM077465)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Physical Sciences › Chemistry › Spectroscopy › Advanced Proteomics Techniques and Applications
- Keywords
- mitochondrial proteins, mitochondrial proteome, Bayesian integration, epitope tagging, literature curation
- MeSH terms
- Animals, Bayes Theorem, Humans, Internet, Genomics, Mitochondrial Proteins, Databases, Protein, Mice
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