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Deficiency of glutaredoxin 5 reveals Fe-S clusters are required for vertebrate haem synthesis.
Abstract
Iron is required to produce haem and iron-sulphur (Fe-S) clusters, processes thought to occur independently. Here we show that the hypochromic anaemia in shiraz (sir) zebrafish mutants is caused by deficiency of glutaredoxin 5 (grx5), a gene required in yeast for Fe-S cluster assembly. We found that grx5 was expressed in erythroid cells of zebrafish and mice. Zebrafish grx5 rescued the assembly of grx5 yeast Fe-S, showing that the biochemical function of grx5 is evolutionarily conserved. In contrast to yeast, vertebrates use iron regulatory protein 1 (IRP1) to sense intracellular iron and regulate mRNA stability or the translation of iron metabolism genes. We found that loss of Fe-S cluster assembly in sir animals activated IRP1 and blocked haem biosynthesis catalysed by aminolaevulinate synthase 2 (ALAS2). Overexpression of ALAS2 RNA without the 5' iron response element that binds IRP1 rescued sir embryos, whereas overexpression of ALAS2 including the iron response element did not. Further, antisense knockdown of IRP1 restored sir embryo haemoglobin synthesis. These findings uncover a connection between haem biosynthesis and Fe-S clusters, indicating that haemoglobin production in the differentiating red cell is regulated through Fe-S cluster assembly.
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“Perhaps less surprising, the clinical phenotype of a unique patient carrying a GLRX5 mutation also differs somewhat from an earlier animal model with a deletion of that gene, the shiraz zebrafish.177”
From Forging a field: the golden age of iron biology. (2008) · cites this paper as [177]
Citations
Cites
Iron-sulfur clusters: nature's modular, multipurpose structures
Beinert, H., Holm, R. H., & Münck, E. (1997) · Science · doi:10.1126/science.277.5326.653 · Cited by 1,944
Hentze, M. W., Muckenthaler, M. U., & Andrews, N. C. (2004) · Cell · doi:10.1016/s0092-8674(04)00343-5 · Cited by 1,736
Mootha, V. K., Bunkenborg, J., Olsen, J. V., Hjerrild, M., Wisniewski, J. R., Stahl, E., Bolouri, M. S., Ray, H. N., Sihag, S., Kamal, M., et al. (2003) · Cell · doi:10.1016/s0092-8674(03)00926-7 · Cited by 889
The mitochondrial proteins Atm1p and Nfs1p are essential for biogenesis of cytosolic Fe/S proteins
Kispál, G., Csere, P., Prohl, C., & Lill, R. (1999) · The EMBO Journal · doi:10.1093/emboj/18.14.3981 · Cited by 699
Fernandes, A. P., & Holmgren, A. (2004) · Antioxidants and Redox Signaling · doi:10.1089/152308604771978354 · Cited by 670
Grx5 Is a Mitochondrial Glutaredoxin Required for the Activity of Iron/Sulfur Enzymes
Rodrı́guez-Manzaneque, M. T., Tamarit, J., Bellı́, G., Ros, J., & Herrero, E. (2002) · Molecular Biology of the Cell · doi:10.1091/mbc.01-10-0517 · Cited by 464
Allikmets, R. L., Raskind, W. H., Hutchinson, A. A., Schueck, N. D., Dean, M. C., & Koeller, D. M. (1999) · Human Molecular Genetics · doi:10.1093/hmg/8.5.743 · Cited by 400
Mühlenhoff, U., Gerber, J., Richhardt, N., & Lill, R. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg446 · Cited by 383
Maturation of cellular Fe–S proteins: an essential function of mitochondria
Lill, R., & Kispal, G. (2000) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(00)01589-9 · Cited by 358
Dernbach, E., Urbich, C., Brandes, R. P., Hofmann, W. K., Zeiher, A. M., & Dimmeler, S. (2004) · Blood · doi:10.1182/blood-2003-12-4103 · Cited by 331
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Items 101–200 of 369
Moseler, A., Aller, I., Wagner, S., Nietzel, T., Przybyla‐Toscano, J., Mühlenhoff, U., Lill, R., Berndt, C., Rouhier, N., Schwarzländer, M., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1510835112 · Cited by 108
Zhang, P., Wu, J., Xiao, F., Zhao, D., & Luan, Y. (2018) · Medicinal Research Reviews · doi:10.1002/med.21485 · Cited by 108
Mammalian Fe–S cluster biogenesis and its implication in disease
Beilschmidt, L. K., & Puccio, H. M. (2014) · Biochimie · doi:10.1016/j.biochi.2014.01.009 · Cited by 113
Cellular and mitochondrial iron homeostasis in vertebrates
Chen, C., & Paw, B. H. (2012) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2012.01.003 · Cited by 111
Mitochondrial Mayhem: The Mitochondrion as a Modulator of Iron Metabolism and Its Role in Disease
Huang, M. L.-H., Lane, D. J. R., & Richardson, D. R. (2011) · Antioxidants & Redox Signaling · doi:10.1089/ars.2011.3921 · Cited by 103
Congenital Sideroblastic Anemias: Iron and Heme Lost in Mitochondrial Translation
Fleming, M. D. (2011) · Hematology · doi:10.1182/asheducation-2011.1.525 · Cited by 103
Iron–Sulfur Clusters: Biogenesis, Molecular Mechanisms, and Their Functional Significance
Xu, X. M., & Møller, S. G. (2010) · Antioxidants and Redox Signaling · doi:10.1089/ars.2010.3259 · Cited by 102
Substrate interactions with human ferrochelatase
Medlock, A. E., Swartz, L., Dailey, T. A., Dailey, H. A., & Lanzilotta, W. N. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0606144104 · Cited by 102
How Does Iron–Sulfur Cluster Coordination Regulate the Activity of Human Glutaredoxin 2?
Berndt, C., Hudemann, C., Hanschmann, E.-M., Axelsson, R., Holmgren, A., & Lillig, C. H. (2006) · Antioxidants and Redox Signaling · doi:10.1089/ars.2007.9.151 · Cited by 101
Iron–sulfur cluster biosynthesis and trafficking – impact on human disease conditions
Wachnowsky, C., Fidai, I., & Cowan, J. A. (2017) · Metallomics · doi:10.1039/c7mt00180k · Cited by 99
Compartmentalization of iron between mitochondria and the cytosol and its regulation
Mühlenhoff, U., Hoffmann, B., Richter, N., Rietzschel, N., Spantgar, F., Stehling, O., Uzarska, M. A., & Lill, R. (2015) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2015.05.003 · Cited by 95
Hydrogen Peroxide and Redox Regulation of Developments
Rampon, C., Volovitch, M., Joliot, A., & Vriz, S. (2018) · Antioxidants · doi:10.3390/antiox7110159 · Cited by 101
Analysis of iron–sulfur protein maturation in eukaryotes
Pierik, A. J., Netz, D. J. A., & Lill, R. (2009) · Nature Protocols · doi:10.1038/nprot.2009.39 · Cited by 94
Iron‐responsive degradation of iron‐regulatory protein 1 does not require the Fe–S cluster
Clarke, S. L., Vasanthakumar, A., Anderson, S. A., Pondarré, C., Koh, C. M., Deck, K. M., Pitula, J. S., Epstein, C. J., Fleming, M. D., & Eisenstein, R. S. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7600954 · Cited by 97
Heme metabolism and erythropoiesis
Chung, J., Chen, C., & Paw, B. H. (2012) · Current Opinion in Hematology · doi:10.1097/moh.0b013e328351c48b · Cited by 96
CpSufE Activates the Cysteine Desulfurase CpNifS for Chloroplastic Fe-S Cluster Formation
Ye, H., Abdel‐Ghany, S. E., Anderson, T. D., Pilon‐Smits, E. A. H., & Pilon, M. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m512737200 · Cited by 93
A Small Molecule Inhibitor of Redox-Regulated Protein Translocation into Mitochondria
Dabir, D. V., Hasson, S. A., Setoguchi, K., Johnson, M. E., Wongkongkathep, P., Douglas, C. J., Zimmerman, J., Damoiseaux, R. D., Teitell, M. A., & Koehler, C. M. (2013) · Developmental Cell · doi:10.1016/j.devcel.2013.03.006 · Cited by 92
Special delivery: distributing iron in the cytosol of mammalian cells
Philpott, C. C., & Ryu, M. (2014) · Frontiers in Pharmacology · doi:10.3389/fphar.2014.00173 · Cited by 96
Vertebrate-specific glutaredoxin is essential for brain development
Bräutigam, L., Schütte, L. D., Godoy, J. R., Prozorovski, T., Gellert, M., Hauptmann, G., Holmgren, A., Lillig, C. H., & Berndt, C. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1110085108 · Cited by 91
Hereditary Sideroblastic Anemias: Pathophysiology, Diagnosis, and Treatment
Camaschella, C. (2009) · Seminars in Hematology · doi:10.1053/j.seminhematol.2009.07.001 · Cited by 92
Mitochondrial dysfunction: a neglected component of skin diseases
Feichtinger, R. G., Sperl, W., Bauer, J. W., & Kofler, B. (2014) · Experimental Dermatology · doi:10.1111/exd.12484 · Cited by 94
Schranzhofer, M., Schifrer, M., Cabrera, J. A., Kopp, S., Chiba, P., Beug, H., & Müllner, E. W. (2006) · Blood · doi:10.1182/blood-2005-05-1809 · Cited by 89
Molina‐Navarro, M. M., Casas, C., Piedrafita, L., Bellı́, G., & Herrero, E. (2006) · FEBS Letters · doi:10.1016/j.febslet.2006.03.037 · Cited by 87
Frey, A. G., Palenchar, D. J., Wildemann, J. D., & Philpott, C. C. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.744946 · Cited by 87
Rogers, J. T., Mikkilineni, S., Cantuti‐Castelvetri, I., Smith, D. H., Huang, X., Bandyopadhyay, S., Cahill, C. M., Maccecchini, M. L., Lahiri, D. K., & Greig, N. H. (2011) · Journal of Neural Transmission · doi:10.1007/s00702-010-0513-5 · Cited by 82
Molecular basis for the distinct functions of redox-active and FeS-transfering glutaredoxins
Trnka, D., Engelke, A. D., Gellert, M., Moseler, A., Hossain, M. F., Lindenberg, T. T., Pedroletti, L., Odermatt, B., de Souza, J. V. B., Bronowska, A. K., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-17323-0 · Cited by 85
Lukosz, M., Jakob, S., Büchner, N., Zschauer, T.-C., Altschmied, J., & Haendeler, J. (2009) · Antioxidants and Redox Signaling · doi:10.1089/ars.2009.2609 · Cited by 83
Lee, D. W., Kaur, D., Chinta, S. J., Rajagopalan, S., & Andersen, J. K. (2009) · Antioxidants and Redox Signaling · doi:10.1089/ars.2009.2489 · Cited by 81
Srinivasan, V., Netz, D. J. A., Webert, H., Mascarenhas, J., Pierik, A. J., Michel, H., & Lill, R. (2007) · Structure · doi:10.1016/j.str.2007.08.009 · Cited by 79
Mitochondrial iron overload: causes and consequences
Rouault, T. A. (2016) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2016.02.004 · Cited by 80
López‐Maury, L., Sánchez-Riego, A. M., Reyes, J. C., & Florencio, F. J. (2009) · Journal of Bacteriology · doi:10.1128/jb.01798-08 · Cited by 77
Recent advances in the understanding of inherited sideroblastic anaemia
Camaschella, C. (2008) · British Journal of Haematology · doi:10.1111/j.1365-2141.2008.07290.x · Cited by 79
From the discovery to molecular understanding of cellular iron-sulfur protein biogenesis
Lill, R. (2020) · Biological Chemistry · doi:10.1515/hsz-2020-0117 · Cited by 73
Iron: Effect of Overload and Deficiency
Hider, R. C., & Kong, X. (2013) · Metal ions in life sciences · doi:10.1007/978-94-007-7500-8_8 · Cited by 78
Iron-Dependent Degradation of Apo-IRP1 by the Ubiquitin-Proteasome Pathway
Wang, J., Fillebeen, C., Chen, G., Biederbick, A., Lill, R., & Pantopoulos, K. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.01111-06 · Cited by 72
Talib, E. A., & Outten, C. E. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2020.118847 · Cited by 68
Xuan, W., Pan, R., Wei, Y., Cao, Y., Li, H., Liang, F., Liu, K., & Wang, W. (2015) · Bioconjugate Chemistry · doi:10.1021/acs.bioconjchem.5b00259 · Cited by 72
Cheng, N., Zhang, W., Chen, W., Jin, J., Cui, X., Butte, N. F., Chan, L., & Hirschi, K. D. (2011) · FEBS Journal · doi:10.1111/j.1742-4658.2011.08178.x · Cited by 71
Goforth, J. B., Anderson, S. A., Nizzi, C. P., & Eisenstein, R. S. (2010) · RNA · doi:10.1261/rna.1857210 · Cited by 71
Ring sideroblasts and sideroblastic anemias
Cazzola, M., & Invernizzi, R. (2011) · Haematologica · doi:10.3324/haematol.2011.044628 · Cited by 71
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Ulrich, D. L., Lynch, J., Wang, Y., Fukuda, Y., Nachagari, D., Du, G., Sun, D., Fan, Y., Tsurkan, L. G., Potter, P. M., et al. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.336180 · Cited by 71
Friedreich's ataxia: the vicious circle hypothesis revisited
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Hematopoietic defects in rps29 mutant zebrafish depend upon p53 activation
Taylor, A. M., Humphries, J. M., White, R. M., Murphey, R. D., Burns, C. E., & Zon, L. I. (2011) · Experimental Hematology · doi:10.1016/j.exphem.2011.11.007 · Cited by 68
Iron homeostasis: new players, newer insights
Edison, E. S., Bajel, A. R., & Chandy, M. (2008) · European Journal Of Haematology · doi:10.1111/j.1600-0609.2008.01143.x · Cited by 71
Zebrafish as a model system for mitochondrial biology and diseases
Steele, S. L., Prykhozhij, S. V., & Berman, J. N. (2013) · Translational research · doi:10.1016/j.trsl.2013.08.008 · Cited by 67
S-glutathionylation, friend or foe in cardiovascular health and disease
Rashdan, N. A., Shrestha, B., & Pattillo, C. B. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101693 · Cited by 64
Comini, M. A., Rettig, J., Dirdjaja, N., Hanschmann, E.-M., Berndt, C., & Krauth‐Siegel, R. L. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m802010200 · Cited by 68
Izquierdo, A., Casas, C., Mühlenhoff, U., Lillig, C. H., & Herrero, E. (2008) · Eukaryotic Cell · doi:10.1128/ec.00133-08 · Cited by 66
Ferrochelatase: Mapping the Intersection of Iron and Porphyrin Metabolism in the Mitochondria
Obi, C. D., Bhuiyan, T., Dailey, H. A., & Medlock, A. E. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.894591 · Cited by 65
Cheng, C. N., & Wingert, R. A. (2014) · Developmental Biology · doi:10.1016/j.ydbio.2014.12.020 · Cited by 63
Nexus between mitochondrial function, iron, copper and glutathione in Parkinson's disease
Liddell, J. R., & White, A. R. (2017) · Neurochemistry International · doi:10.1016/j.neuint.2017.05.016 · Cited by 64
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Kafina, M. D., & Paw, B. H. (2017) · Metallomics · doi:10.1039/c7mt00103g · Cited by 65
Abu-Zeinah, G. F., & DeSancho, M. T. (2020) · Journal of Blood Medicine · doi:10.2147/jbm.s232644 · Cited by 63
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Camaschella, C., & Poggiali, E. (2011) · Current Opinion in Pediatrics · doi:10.1097/mop.0b013e3283425591 · Cited by 59
Lind, M., Missirlis, F., Melefors, Ö., Uhrigshardt, H., Kirby, K., Phillips, J. P., Söderhäll, K., & Rouault, T. A. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m603354200 · Cited by 60
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Richardson, D. R., Huang, M. L. H., Whitnall, M., Becker, E., Ponka, P., & Rahmanto, Y. S. (2009) · Journal of Molecular Medicine · doi:10.1007/s00109-009-0565-x · Cited by 59
Riondet, C., de Souris, J. P., Guilleminot, J., Chartier, Y., Meyer, Y., & Reichheld, J. (2011) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2011.02355.x · Cited by 58
Willems, P. H. G. M., Wanschers, B. F. J., Esseling, J. J., Szklarczyk, R., Kudla, U., Duarte, I., Forkink, M., Nooteboom, M., Swarts, H. G. P., Gloerich, J., et al. (2012) · Antioxidants and Redox Signaling · doi:10.1089/ars.2011.4253 · Cited by 58
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Sebastiani, G., & Pantopoulos, K. (2011) · Metallomics · doi:10.1039/c1mt00082a · Cited by 58
Martins, L. M., Knuesting, J., Bariat, L., Dard, A., Freibert, S., Marchand, C. H., Young, D., Dung, N. H. T., Voth, W., de Bures, A., et al. (2020) · PLANT PHYSIOLOGY · doi:10.1104/pp.20.00906 · Cited by 57
Redox properties and evolution of human glutaredoxins
Sagemark, J., Elgán, T. H., Bürglin, T. R., Johansson, C., Holmgren, A., & Berndt, K. D. (2007) · Proteins Structure Function and Bioinformatics · doi:10.1002/prot.21416 · Cited by 58
Zhang, B., Bandyopadhyay, S., Shakamuri, P., Naik, S., Huynh, B. H., Couturier, J., Rouhier, N., & Johnson, M. K. (2013) · Journal of the American Chemical Society · doi:10.1021/ja407059n · Cited by 56
Nie, G., Chen, G., Sheftel, A. D., Pantopoulos, K., & Ponka, P. (2006) · Blood · doi:10.1182/blood-2006-04-018341 · Cited by 56
Marelja, Z., Leimkühler, S., & Missirlis, F. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00050 · Cited by 61
Seco-Cervera, M., González‐Cabo, P., Pallardó, F. V., Mateo, C. R., & García‐Giménez, J. L. (2020) · Antioxidants · doi:10.3390/antiox9121257 · Cited by 57
Fixing frataxin: ‘ironing out’ the metabolic defect in F riedreich's ataxia
Anzovino, A., Lane, D. J. R., Huang, M., & Richardson, D. R. (2013) · British Journal of Pharmacology · doi:10.1111/bph.12470 · Cited by 56
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Hoffmann, B., Uzarska, M. A., Berndt, C., Godoy, J. R., Haunhorst, P., Lillig, C. H., Lill, R., & Mühlenhoff, U. (2011) · Antioxidants and Redox Signaling · doi:10.1089/ars.2010.3811 · Cited by 55
Iron Metabolism and Its Disorders
Harvey, J. W. (2008) · Elsevier eBooks · doi:10.1016/b978-0-12-370491-7.00009-x · Cited by 57
Ferring–Appel, D., Hentze, M. W., & Galy, B. (2008) · Blood · doi:10.1182/blood-2008-05-155093 · Cited by 53
Pathophysiology and genetic mutations in congenital sideroblastic anemia
Fujiwara, T., & Harigae, H. (2013) · Pediatrics International · doi:10.1111/ped.12217 · Cited by 53
Marra, A. N., & Wingert, R. A. (2016) · Developmental Biology · doi:10.1016/j.ydbio.2016.01.035 · Cited by 53
Fosset, C., Chauveau, M.-J., Guillon, B., Canal, F., Drapier, J., & Bouton, C. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m602979200 · Cited by 56
Rare anemias due to genetic iron metabolism defects
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Mühlenhoff, U., Braymer, J. J., Christ, S., Rietzschel, N., Uzarska, M. A., Weiler, B. D., & Lill, R. (2020) · Biological Chemistry · doi:10.1515/hsz-2020-0237 · Cited by 52
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Lepka, K., Volbracht, K., Bill, E., Schneider, R., Ríos, N., Hildebrandt, T., Ingwersen, J., Prozorovski, T., Lillig, C. H., van Horssen, J., et al. (2017) · Glia · doi:10.1002/glia.23178 · Cited by 49
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Maio, N., Zhang, D., Ghosh, M. C., Jain, A., SantaMaria, A. M., & Rouault, T. A. (2021) · Seminars in Hematology · doi:10.1053/j.seminhematol.2021.06.001 · Cited by 50
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Linares, G. R., Xing, W., Govoni, K. E., Chen, S., & Mohan, S. (2009) · Bone · doi:10.1016/j.bone.2009.01.003 · Cited by 48
Sheftel, A. D., & Lill, R. (2008) · Annals of Medicine · doi:10.1080/07853890802322229 · Cited by 49
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Synthesis, delivery and regulation of eukaryotic heme and Fe–S cluster cofactors
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Chung, J., Wittig, J. G., Ghamari, A., Maeda, M., Dailey, T. A., Bergonia, H. A., Kafina, M. D., Coughlin, E. E., Minogue, C. E., Hebert, A. S., et al. (2017) · eLife · doi:10.7554/elife.24767 · Cited by 47
Nordin, A., Larsson, E., Thornell, L., & Holmberg, M. (2010) · Human Genetics · doi:10.1007/s00439-010-0931-3 · Cited by 45
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Oceans of opportunity: Exploring vertebrate hematopoiesis in zebrafish
Carroll, K. J., & North, T. E. (2014) · Experimental Hematology · doi:10.1016/j.exphem.2014.05.002 · Cited by 47
Paul, B. T., Tesfay, L., Winkler, C. R., Torti, F. M., & Torti, S. V. (2019) · Scientific Reports · doi:10.1038/s41598-019-55907-z · Cited by 45
How I manage patients with atypical microcytic anaemia
Camaschella, C. (2013) · British Journal of Haematology · doi:10.1111/bjh.12081 · Cited by 49
Iwaï, K. (2018) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2018.09.011 · Cited by 46
Filser, M., Comini, M. A., Molina‐Navarro, M. M., Dirdjaja, N., Herrero, E., & Krauth‐Siegel, R. L. (2007) · Biological Chemistry · doi:10.1515/bc.2007.147 · Cited by 43
Functional Analysis of GLRX5 Mutants Reveals Distinct Functionalities of GLRX5 Protein
Liu, G., Wang, Y., Anderson, G. J., Camaschella, C., Chang, Y., & Nie, G. (2015) · Journal of Cellular Biochemistry · doi:10.1002/jcb.25267 · Cited by 43
Yien, Y. Y., Shi, J., Chen, C., Cheung, J., Grillo, A. S., Shrestha, R., Li, L., Zhang, X., Kafina, M. D., Kingsley, P. D., et al. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.002742 · Cited by 46
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Metadata
- Authors
- The Tübingen 2000 Screen Consortium, Wingert, R. A., Galloway, J. L., Barut, B., Foott, H., Fraenkel, P., Axe, J. L., Weber, G. J., Dooley, K., Davidson, A. J., Schmidt, B., Paw, B. H., Shaw, G. C., Kingsley, P., Palis, J., Schubert, H., Chen, O., Kaplan, J., & Zon, L. I.
- Affiliations
- Howard Hughes Medical Institute (US)
- Brigham and Women's Hospital (US)
- University of Rochester Medicine (US)
- University of Utah (US)
- Corresponding author
- Zon, Leonard I.
- ORCID
- Venue
- Nature
- Published
- 2005-08-18
- Volume
- 436
- Issue
- 7053
- Pages
- 1035-1039
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W1992193197
- Cited by
- 370
- References
- 33
- Citations by year
- 2026: 6 · 2025: 1 · 2024: 8 · 2023: 6 · 2022: 11 · 2021: 15 · 2020: 17 · 2019: 11 · 2018: 14 · 2017: 17 · 2016: 15 · 2015: 13 · 2014: 18 · 2013: 17 · 2012: 21
- FWCI
- 16.29
- Type
- journal article
- Language
- en
- Update notices
- erratum (2005-10-06)
- Open access
- closed
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- Albert J. Ryan Foundation
- Harvard University
- National Institutes of Health
- Topics
- Health Sciences › Medicine › Hematology › Iron Metabolism and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Hemoglobin structure and function
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Metalloenzymes and iron-sulfur proteins
- Keywords
- heme biosynthesis, iron regulatory protein 1, erythroid cells, hypochromic anemia, iron-responsive element, hemoglobin synthesis, iron metabolism regulation
- MeSH terms
- Amino Acid Sequence, 5-Aminolevulinate Synthetase, Animals, Cloning, Molecular, Erythrocytes, Gene Expression Regulation, Heme, Homeostasis, Iron, Iron-Sulfur Proteins, Molecular Sequence Data, Oxidoreductases, Saccharomyces cerevisiae, Zebrafish, Response Elements, Iron Regulatory Protein 1, Mice, Glutaredoxins
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