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A systematic RNAi screen identifies a critical role for mitochondria in C. elegans longevity
Abstract
We report a systematic RNA interference (RNAi) screen of 5,690 Caenorhabditis elegans genes for gene inactivations that increase lifespan. We found that genes important for mitochondrial function stand out as a principal group of genes affecting C. elegans lifespan. A classical genetic screen identified a mutation in the mitochondrial leucyl-tRNA synthetase gene (lrs-2) that impaired mitochondrial function and was associated with longer-lifespan. The long-lived worms with impaired mitochondria had lower ATP content and oxygen consumption, but differential responses to free-radical and other stresses. These data suggest that the longer lifespan of C. elegans with compromised mitochrondria cannot simply be assigned to lower free radical production and suggest a more complex coupling of metabolism and longevity.
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“Unexpectedly, reduced mitochondrial function can, in some circumstances, increase lifespan.”
From Neural mechanisms of ageing and cognitive decline (2010) · cites this paper as [36]
In the citing paper
“Paradoxically, it is the impairment of mitochondrial function and associated lower ATP levels that prolongs lifespan in worms (Dillin et al., 2002; Lee et al., 2003).”
From The Search for Antiaging Interventions: From Elixirs to Fasting Regimens (2014) · cites this paper as Lee et al., 2003
In the citing paper
“an unbiased search for genes that extend lifespan has identified a disproportionate number of genes that function in mitochondrial metabolism(273)”
From Metformin, the Aspirin of the 21st Century: Its Role in Gestational Diabetes Mellitus, Prevention of Preeclampsia and Cancer, and the Promotion of Longevity (2017) · cites this paper as [273]
In the citing paper
“By contrast, knockdown experiments that target other components of the electron transport chain, including essential elements of complexes I, III and IV, lead to lifespan extension in worms 99, 100 .”
From The common biology of cancer and ageing (2007) · cites this paper as [100]
Citations
Cites
Oxidants, oxidative stress and the biology of ageing
Finkel, T., & Holbrook, N. J. (2000) · Nature · doi:10.1038/35041687 · Cited by 9,413
Systematic functional analysis of the Caenorhabditis elegans genome using RNAi
Kamath, R. S., Fraser, A. G., Yan, D., Poulin, G. B., Durbin, R. M., Gotta, M., Kanapin, A. A., Bot, N. L., Moreno, S., Sohrmann, M., et al. (2003) · Nature · doi:10.1038/nature01278 · Cited by 3,618
Self-citationA C. elegans mutant that lives twice as long as wild type
Kenyon, C., Chang, J., Gensch, E., Rudner, A., & Tabtiang, R. (1993) · Nature · doi:10.1038/366461a0 · Cited by 3,387
Mitochondrial diseases in man and mouse
Wallace, D. C. (1999) · Science · doi:10.1126/science.283.5407.1482 · Cited by 3,060
Kimura, K. D., Tissenbaum, H. A., Liu, Y., & Ruvkun, G. (1997) · Science · doi:10.1126/science.277.5328.942 · Cited by 2,250
Self-citationOgg, S., Paradis, S., Gottlieb, S., Patterson, G. I., Lee, L., Tissenbaum, H. A., & Ruvkun, G. (1997) · Nature · doi:10.1038/40194 · Cited by 1,935
Self-citationFunctional genomic analysis of C. elegans chromosome I by systematic RNA interference
Fraser, A. G., Kamath, R. S., Zipperlen, P., Martinez-Campos, M., Sohrmann, M., & Ahringer, J. (2000) · Nature · doi:10.1038/35042517 · Cited by 1,720
Self-citationLin, K., Dorman, J. B., Rodan, A. R., & Kenyon, C. J. (1997) · Science · doi:10.1126/science.278.5341.1319 · Cited by 1,501
Longevity, senescence and the genome
(1995) · General Pharmacology The Vascular System · doi:10.1016/0306-3623(95)90026-8 · Cited by 1,403
Genetic pathways that regulate ageing in model organisms
Guarente, L., & Kenyon, C. J. (2000) · Nature · doi:10.1038/35041700 · Cited by 1,337
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Uittenbogaard, M. N., & Chiaramello, A. (2014) · Current Pharmaceutical Design · doi:10.2174/1381612820666140305224906 · Cited by 246
Recent developments in yeast aging
Kaeberlein, M., Burtner, C. R., & Kennedy, B. K. (2007) · PLoS Genetics · doi:10.1371/journal.pgen.0030084 · Cited by 239
Pleiotropic effects of mitochondria in aging
de Lima, T. I., Li, T. Y., Mottis, A., & Auwerx, J. H. (2022) · Nature Aging · doi:10.1038/s43587-022-00191-2 · Cited by 254
Bitterman, K. J., Medvedik, O., & Sinclair, D. A. (2003) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.67.3.376-399.2003 · Cited by 240
Mitochondria in the signaling pathways that control longevity and health span
Akbari, M., Kirkwood, T. B. L., & Bohr, V. A. (2019) · Ageing Research Reviews · doi:10.1016/j.arr.2019.100940 · Cited by 234
Using C. elegans for aging research
Tissenbaum, H. A. (2014) · Invertebrate Reproduction & Development · doi:10.1080/07924259.2014.940470 · Cited by 245
Adaptive homeostasis and the free radical theory of ageing
Pomatto, L. C. D., & Davies, K. J. A. (2018) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2018.06.016 · Cited by 233
Causal roles of mitochondrial dynamics in longevity and healthy aging
Sharma, A., Smith, H. J., Yao, P., & Mair, W. B. (2019) · EMBO Reports · doi:10.15252/embr.201948395 · Cited by 222
Human Aging and Longevity Are Characterized by High Levels of Mitokines
Conte, M., Ostan, R., Fabbri, C., Santoro, A., Guidarelli, G., Vitale, G., Mari, D., Sevini, F., Capri, M., Sandri, M., et al. (2019) · The Journals of Gerontology: Series A · doi:10.1093/gerona/gly153 · Cited by 219
Mitochondrial Permeability Uncouples Elevated Autophagy and Lifespan Extension
Zhou, B., Kreuzer, J., Kumsta, C., Wu, L., Kamer, K. J., Cedillo, L., Zhang, Y., Li, S., Kacergis, M. C., Webster, C. M., et al. (2019) · Cell · doi:10.1016/j.cell.2019.02.013 · Cited by 220
Artal‐Sanz, M., Tsang, W. Y., Willems, E., Grivell, L. A., Lemire, B. D., van der Spek, H., & Nijtmans, L. G. J. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m304877200 · Cited by 220
Hanover, J. A., Forsythe, M. E., Hennessey, P. T., Brodigan, T. M., Love, D. C., Ashwell, G., & Krause, M. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0408771102 · Cited by 218
Metabolic networks of longevity
Houtkooper, R. H., Williams, R. W., & Auwerx, J. (2010) · Cell · doi:10.1016/j.cell.2010.06.029 · Cited by 217
Bennett, C. F., Wende, H. V., Simko, M., Klum, S., Barfield, S., Choi, H., Pineda, V. V., & Kaeberlein, M. R. (2014) · Nature Communications · doi:10.1038/ncomms4483 · Cited by 220
Pierce, S. B., Geršak, K., Michaelson‐Cohen, R., Walsh, T., Lee, M. K., Malach, D., Klevit, R. E., King, M., & Levy‐Lahad, E. (2013) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2013.03.007 · Cited by 216
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Cullen, L. M., & Arndt, G. M. (2005) · Immunology and Cell Biology · doi:10.1111/j.1440-1711.2005.01332.x · Cited by 213
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Lapointe, J., & Hekimi, S. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m803287200 · Cited by 212
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Wolff, S., Ma, H., Burch, D., Maciel, G. A. R., Hunter, T. R., & Dillin, A. G. (2006) · Cell · doi:10.1016/j.cell.2005.12.042 · Cited by 208
Yang, J., Huang, T., Petralia, F., Long, Q., Zhang, B., Argmann, C., Zhao, Y. B., Mobbs, C. V., Schadt, E. E., Zhu, J., et al. (2015) · Scientific Reports · doi:10.1038/srep15145 · Cited by 200
Boulias, K., & Horvitz, H. R. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.02.014 · Cited by 184
Lifespan-regulating genes in C. elegans
Uno, M., & Nishida, E. (2016) · npj Aging and Mechanisms of Disease · doi:10.1038/npjamd.2016.10 · Cited by 202
Mitochondrial proteostasis in the context of cellular and organismal health and aging
Moehle, E. A., Shen, K., & Dillin, A. G. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.tm117.000893 · Cited by 200
Modulated microRNA expression during adult lifespan in Caenorhabditis elegans
Ibáñez‐Ventoso, C., Yang, M., Guo, S., Robins, H. S., Padgett, R. W., & Driscoll, M. (2006) · Aging Cell · doi:10.1111/j.1474-9726.2006.00210.x · Cited by 194
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Antebi, A. (2007) · PLoS Genetics · doi:10.1371/journal.pgen.0030129 · Cited by 190
Measuring Caenorhabditis elegans Life Span on Solid Media
Sutphin, G. L., & Kaeberlein, M. R. (2009) · Journal of Visualized Experiments · doi:10.3791/1152 · Cited by 191
Longevity and stress in Caenorhabditis elegans
Zhou, K. I., Pincus, Z., & Slack, F. J. (2011) · Aging · doi:10.18632/aging.100367 · Cited by 196
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Mousses, S., Caplen, N. J., Cornelison, R., Weaver, D., Basik, M., Hautaniemi, S., Elkahloun, A. G., Lotufo, R., Choudary, A., Dougherty, E. R., et al. (2003) · Genome Research · doi:10.1101/gr.1478703 · Cited by 189
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Zheng, L., Liu, J., Batalov, S., Zhou, D., Orth, A. P., Ding, S., & Schultz, P. G. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2136685100 · Cited by 188
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Koopman, M., Michels, H., Dancy, B. M., Kamble, R., Mouchiroud, L., Auwerx, J. H., Nollen, E. A. A., & Houtkooper, R. H. (2016) · Nature Protocols · doi:10.1038/nprot.2016.106 · Cited by 180
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Rossmann, M. P., Dubois, S. M., Agarwal, S., & Zon, L. I. (2021) · Disease Models & Mechanisms · doi:10.1242/dmm.048912 · Cited by 200
Fukui, H., Diaz, F., Garcia, S., & Moraes, C. T. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705738104 · Cited by 185
Fridell, Y.-W. C., Sánchez-Blanco, A., Silvia, B. A., & Helfand, S. L. (2005) · Cell Metabolism · doi:10.1016/j.cmet.2005.01.005 · Cited by 185
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Paek, J., Lo, J. Y., Narasimhan, S. D., Nguyen, T. N., Glover-Cutter, K. M., Robida-Stubbs, S., Suzuki, T., Yamamoto, M. P., Blackwell, T. K., & Curran, S. P. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.09.007 · Cited by 183
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Sohal, R. S., & Forster, M. J. (2014) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2014.05.015 · Cited by 187
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Wall, N. R., & Shi, Y. (2003) · The Lancet · doi:10.1016/s0140-6736(03)14637-5 · Cited by 181
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Yang, W., Li, J., & Hekimi, S. (2007) · Genetics · doi:10.1534/genetics.107.080788 · Cited by 171
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Jazwinski, S. M. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2012.02.010 · Cited by 172
Vellai, T. (2008) · Cell Death and Differentiation · doi:10.1038/cdd.2008.126 · Cited by 173
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Senchuk, M. M., Dues, D. J., Schaar, C. E., Johnson, B. K., Madaj, Z., Bowman, M. J., Winn, M. E., & Raamsdonk, J. M. V. (2018) · PLoS Genetics · doi:10.1371/journal.pgen.1007268 · Cited by 184
Zhang, P., Judy, M. E., Lee, S., & Kenyon, C. J. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2012.12.013 · Cited by 167
Self-citationMitohormesis, an Antiaging Paradigm
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da Cunha, F. M., Torelli, N. Q., & Kowaltowski, A. J. (2015) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2015/482582 · Cited by 171
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Narasimhan, S. D., Yen, K., & Tissenbaum, H. A. (2009) · Current Biology · doi:10.1016/j.cub.2009.06.013 · Cited by 169
Qin, G., Meng, X., Wang, Q., & Tian, S. (2009) · Journal of Proteome Research · doi:10.1021/pr801046m · Cited by 167
RNA interference microarrays: High-throughput loss-of-function genetics in mammalian cells
Silva, J. M., Mizuno, H., Brady, A., Lucito, R., & Hannon, G. J. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0400165101 · Cited by 167
Cristina, D., Cary, M., Lunceford, A., Clarke, C., & Kenyon, C. (2009) · PLoS Genetics · doi:10.1371/journal.pgen.1000450 · Cited by 166
Labbadia, J. P., Brielmann, R. M., Neto, M. F., Lin, Y.-F., Haynes, C. M., & Morimoto, R. I. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.10.038 · Cited by 167
Xian, H., & Liou, Y. (2020) · Cell Death and Differentiation · doi:10.1038/s41418-020-00657-z · Cited by 177
Yang, Y., Çimen, H., Han, M.-J., Shi, T., Deng, J., Koç, H., Palacios, O. M., Montier, L., Bai, Y., Tong, Q., et al. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.053421 · Cited by 164
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Shao, L.-W., Niu, R., & Liu, Y. (2016) · Cell Research · doi:10.1038/cr.2016.118 · Cited by 161
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Ma, C., Niu, R., Huang, T., Shao, L.-W., Peng, Y., Ding, W., Wang, Y., Jia, G., He, C., Li, C., et al. (2018) · Nature Cell Biology · doi:10.1038/s41556-018-0238-5 · Cited by 167
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Ni, Z., Ebata, A., Alipanahiramandi, E., & Lee, S. S. (2011) · Aging Cell · doi:10.1111/j.1474-9726.2011.00785.x · Cited by 155
Self-citationTipping the metabolic scales towards increased longevity in mammals
Riera, C. E., & Dillin, A. (2015) · Nature Cell Biology · doi:10.1038/ncb3107 · Cited by 153
Owusu-Ansah, E., & Perrimon, N. (2014) · Disease Models & Mechanisms · doi:10.1242/dmm.012989 · Cited by 156
Molecular hallmarks of heterochronic parabiosis at single-cell resolution
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Artal‐Sanz, M., de Jong, L., & Tavernarakis, N. (2006) · Biotechnology Journal · doi:10.1002/biot.200600176 · Cited by 159
Branched-chain amino acid catabolism is a conserved regulator of physiological ageing
Mansfeld, J., Urban, N., Priebe, S., Groth, M., Frahm, C., Hartmann, N., Gebauer, J., Ravichandran, M., Dommaschk, A., Schmeisser, S., et al. (2015) · Nature Communications · doi:10.1038/ncomms10043 · Cited by 151
Chaudhari, S. N., & Kipreos, E. T. (2017) · Nature Communications · doi:10.1038/s41467-017-00274-4 · Cited by 147
Aboobaker, A. A., & Blaxter, M. (2003) · Molecular and Biochemical Parasitology · doi:10.1016/s0166-6851(03)00092-6 · Cited by 152
Baumgart, M., Priebe, S., Groth, M., Hartmann, N., Menzel, U., Pandolfini, L., Koch, P., Felder, M., Ristow, M., Englert, C., et al. (2016) · Cell Systems · doi:10.1016/j.cels.2016.01.014 · Cited by 150
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Nemoto, S., Combs, C. A., French, S. A., Ahn, B., Fergusson, M. M., Balaban, R. S., & Finkel, T. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m511626200 · Cited by 147
Retrograde signaling is regulated by the dynamic interaction between Rtg2p and Mks1p
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Strange, K. B. (2005) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00598.2004 · Cited by 149
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Kondoh, H., LLeonart, M. E., Bernard, D., & Gil, J. (2007) · PubMed · doi:10.14670/hh-22.85 · Cited by 143
Gems, D., & McElwee, J. J. (2004) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2004.09.001 · Cited by 141
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Chen, D., Pan, K. Z., Palter, J. E., & Kapahi, P. (2007) · Aging Cell · doi:10.1111/j.1474-9726.2007.00305.x · Cited by 138
Hulme, S. E., & Whitesides, G. M. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201005461 · Cited by 141
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Sen, G. L., Wehrman, T. S., Myers, J. W., & Blau, H. M. (2004) · Nature Genetics · doi:10.1038/ng1288 · Cited by 134
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Shore, D. E., & Ruvkun, G. (2013) · Trends in Cell Biology · doi:10.1016/j.tcb.2013.04.007 · Cited by 137
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Huang, H. (2004) · Frontiers in bioscience · doi:10.2741/1298 · Cited by 136
The good and the bad of being connected: the integrons of aging
Dillin, A. G., Gottschling, D. E., & Nyström, T. (2014) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2013.12.003 · Cited by 141
Fleming, T. H., Humpert, P. M., Nawroth, P. P., & Bierhaus, A. (2010) · Gerontology · doi:10.1159/000322087 · Cited by 139
Kumar, S., Egan, B. M., Kocsisova, Z., Schneider, D. L., Murphy, J. T., Diwan, A., & Kornfeld, K. (2019) · Developmental Cell · doi:10.1016/j.devcel.2019.03.010 · Cited by 130
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Carrano, A. C., Liu, Z., Dillin, A. G., & Hunter, T. R. (2009) · Nature · doi:10.1038/nature08130 · Cited by 132
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Ding, C., & Cantor, C. R. (2004) · BMB Reports · doi:10.5483/bmbrep.2004.37.1.001 · Cited by 132
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Pang, S., & Curran, S. P. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2013.12.005 · Cited by 132
Chemistry-to-gene screens in Caenorhabditis elegans
Jones, A. K., Buckingham, S. D., & Sattelle, D. B. (2005) · Nature Reviews Drug Discovery · doi:10.1038/nrd1692 · Cited by 129
McElwee, J. J., Schuster, E. F., Blanc, E., Thornton, J. M., & Gems, D. (2006) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2006.01.006 · Cited by 128
Mitochondrial complex I as a therapeutic target for Alzheimer's disease
Trushina, E. V., Trushin, S., & Hasan, M. F. (2021) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2021.11.003 · Cited by 131
Drugs that modulate aging: the promising yet difficult path ahead
Kennedy, B. K., & Pennypacker, J. K. (2014) · Translational research · doi:10.1016/j.trsl.2013.11.007 · Cited by 127
RNA Interference in Biology and Medicine
Milhavet, O., Gary, D. S., & Mattson, M. P. (2003) · Pharmacological Reviews · doi:10.1124/pr.55.4.1 · Cited by 127
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Murakami, C. J., Burtner, C. R., Kennedy, B. K., & Kaeberlein, M. R. (2008) · The Journals of Gerontology Series A · doi:10.1093/gerona/63.2.113 · Cited by 124
Szewczyk, N. J., Udranszky, I. A., Kozak, E. M., Sunga, J., Kim, S. K., Jacobson, L. A., & Conley, C. A. (2006) · Journal of Experimental Biology · doi:10.1242/jeb.02492 · Cited by 127
Ichishita, R., Tanaka, K., Sugiura, Y., Sayano, T., Mihara, K., & Oka, T. (2008) · The Journal of Biochemistry · doi:10.1093/jb/mvm245 · Cited by 126
Sex-specific regulation of aging and apoptosis
Tower, J. (2006) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2006.05.001 · Cited by 125
Dilberger, B., Baumanns, S., Schmitt, F., Schmiedl, T., Hardt, M., Wenzel, U., & Eckert, G. P. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/6840540 · Cited by 124
What evidence is there for the existence of individual genes with antagonistic pleiotropic effects?
Leroi, A. M., Bartke, A., Benedictis, G. D., Franceschi, C., Gartner, A., Gonos, E. S., Feder, M. E., Kivisild, T., Lee, S. Y., Özer, N. K., et al. (2004) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2004.07.012 · Cited by 121
Self-citationMouse aging cell atlas analysis reveals global and cell type-specific aging signatures
Zhang, M. J., Pisco, A. O., Darmanis, S., & Zou, J. (2021) · eLife · doi:10.7554/elife.62293 · Cited by 121
The role of mitochondria in the life of the nematode, Caenorhabditis elegans
Tsang, W. Y., & Lemire, B. D. (2003) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/s0925-4439(03)00079-6 · Cited by 120
Kim, Y.-S., & Sun, H. (2007) · Aging Cell · doi:10.1111/j.1474-9726.2007.00302.x · Cited by 122
Bratic, I., Hench, J., Henriksson, J., Antebi, A., Bürglin, T. R., & Trifunović, A. (2009) · Nucleic Acids Research · doi:10.1093/nar/gkp018 · Cited by 120
Metadata
- Authors
- Lee, S. S., Lee, R. Y. N., Fraser, A. G., Kamath, R. S., Ahringer, J., & Ruvkun, G.
- Affiliations
- Harvard University (US)
- University of Cambridge (GB)
- Corresponding author
- Ruvkun, Gary
- Venue
- Nature Genetics
- Published
- 2002-11-25
- Volume
- 33
- Issue
- 1
- Pages
- 40-48
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2155265427
- Cited by
- 969
- References
- 47
- Citations by year
- 2026: 18 · 2025: 20 · 2024: 18 · 2023: 26 · 2022: 34 · 2021: 39 · 2020: 34 · 2019: 30 · 2018: 42 · 2017: 32 · 2016: 40 · 2015: 32 · 2014: 43 · 2013: 26 · 2012: 46
- FWCI
- 16.56
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Genetics (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Wellcome Trust (054523)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Keywords
- Caenorhabditis elegans, lifespan, longevity, mitochondria, mitochondrial function, leucyl-tRNA synthetase, RNAi screen, ATP levels, oxygen consumption, free radicals, stress response
- MeSH terms
- Adenosine Triphosphate, Animals, Gene Expression Regulation, Genetic Testing, Leucine-tRNA Ligase, Longevity, Mitochondria, Oxygen Consumption, Stress, Physiological, Caenorhabditis elegans, Genes, Helminth, RNA Interference
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