The DOI matches its Crossref record; 93 of the 94 references it cites were found in a registry or an index.
Candida albicans Hap43 Is a Repressor Induced under Low-Iron Conditions and Is Essential for Iron-Responsive Transcriptional Regulation and Virulence
Open accessAbstract
Candida albicans is an opportunistic fungal pathogen that exists as normal flora in healthy human bodies but causes life-threatening infections in immunocompromised patients. In addition to innate and adaptive immunities, hosts also resist microbial infections by developing a mechanism of “natural resistance” that maintains a low level of free iron to restrict the growth of invading pathogens. C. albicans must overcome this iron-deprived environment to cause infections. There are three types of iron-responsive transcriptional regulators in fungi; Aft1/Aft2 activators in yeast, GATA-type repressors in many fungi, and HapX/Php4 in Schizosaccharomyces pombe and Aspergillus species. In this study, we characterized the iron-responsive regulator Hap43, which is the C. albicans homolog of HapX/Php4 and is repressed by the GATA-type repressor Sfu1 under iron-sufficient conditions. We provide evidence that Hap43 is essential for the growth of C. albicans under low-iron conditions and for C. albicans virulence in a mouse model of infection. Hap43 was not required for iron acquisition under low-iron conditions. Instead, it was responsible for repression of genes that encode iron-dependent proteins involved in mitochondrial respiration and iron-sulfur cluster assembly. We also demonstrated that Hap43 executes its function by becoming a transcriptional repressor and accumulating in the nucleus in response to iron deprivation. Finally, we found a connection between Hap43 and the global corepressor Tup1 in low-iron-induced flavinogenesis. Taken together, our data suggest a complex interplay among Hap43, Sfu1, and Tup1 to coordinately regulate iron acquisition, iron utilization, and other iron-responsive metabolic activities.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“Finally, it has been recently reported that Hap43, Sfu1, and Tup1 act coordinately and regulate iron acquisition, iron utilization, and other iron-responsive metabolic activities in C. albicans [75].”
From Strategies of intracellular pathogens for obtaining iron from the environment (2015) · cites this paper as [75]
Citations
Cites
Clustal W and Clustal X version 2.0
Larkin, M., Blackshields, G., Brown, N. P., Chenna, R., McGettigan, P., McWilliam, H., Valentin, F., Wallace, I. M., Wilm, A., López, R., et al. (2007) · Bioinformatics · doi:10.1093/bioinformatics/btm404 · Cited by 28,598
Oxygen toxicity, oxygen radicals, transition metals and disease
Halliwell, B., & Gutteridge, J. M. C. (1984) · Biochemical Journal · doi:10.1042/bj2190001 · Cited by 5,330
Hentze, M. W., Muckenthaler, M. U., & Andrews, N. C. (2004) · Cell · doi:10.1016/s0092-8674(04)00343-5 · Cited by 1,736
Isogenic strain construction and gene mapping in Candida albicans.
Fonzi, W. A., & Irwin, M. Y. (1993) · Genetics · doi:10.1093/genetics/134.3.717 · Cited by 1,695
Gillum, A. M., Tsay, E. Y. H., & Kirsch, D. R. (1984) · Molecular and General Genetics MGG · doi:10.1007/bf00328721 · Cited by 1,253
Secretion of Flavins by Shewanella Species and Their Role in Extracellular Electron Transfer
von Canstein, H., Ogawa, J., Shimizu, S., & Lloyd, J. R. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.01387-07 · Cited by 912
Biologically relevant metal ion‐dependent hydroxyl radical generation An update
Halliwell, B. B., & Gutteridge, J. M. C. (1992) · FEBS Letters · doi:10.1016/0014-5793(92)80911-y · Cited by 884
MatGAT: An application that generates similarity/identity matrices using protein or DNA sequences
Campanella, J. J., Bitincka, L., & Smalley, J. V. (2003) · BMC Bioinformatics · doi:10.1186/1471-2105-4-29 · Cited by 857
The SAT1 flipper, an optimized tool for gene disruption in Candida albicans
Reuß, O., Vik, Å., Kolter, R., & Morschhäuser, J. (2004) · Gene · doi:10.1016/j.gene.2004.06.021 · Cited by 744
Lack of a role for iron in the Lyme disease pathogen
Posey, J. E., & Gherardini, F. C. (2000) · Science · doi:10.1126/science.288.5471.1651 · Cited by 538
Research works printed but not linked: 1
- SambrookJ. RussellD. W. . 2001. Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.
Cited by
Sorted by citations
The role of mitochondria in cellular iron–sulfur protein biogenesis and iron metabolism
Lill, R., Hoffmann, B., Molik, S., Pierik, A. J., Rietzschel, N., Stehling, O., Uzarska, M. A., Webert, H., Wilbrecht, C., & Mühlenhoff, U. (2012) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2012.05.009 · Cited by 513
Chen, C., Pande, K., French, S. D., Tuch, B. B., & Noble, S. M. (2011) · Cell Host & Microbe · doi:10.1016/j.chom.2011.07.005 · Cited by 314
Gerwien, F., Skrahina, V., Kasper, L., Hube, B., & Brunke, S. (2017) · FEMS Microbiology Reviews · doi:10.1093/femsre/fux050 · Cited by 255
Portrait of Candida albicans Adherence Regulators
Finkel, J. S., Xu, W., Huang, D., Hill, E. M., Desai, J. V., Woolford, C. A., Nett, J. E., Taff, H., Norice, C. T., Andes, D. R., et al. (2012) · PLoS Pathogens · doi:10.1371/journal.ppat.1002525 · Cited by 228
Iron - a key nexus in the virulence of Aspergillus fumigatus
Haas, H. (2012) · Frontiers in Microbiology · doi:10.3389/fmicb.2012.00028 · Cited by 217
López‐Berges, M. S., Capilla, J., Turrà, D., Schafferer, L., Matthijs, S., Jöchl, C., Cornélis, P., Guarro, J., Haas, H., & Pietro, A. D. (2012) · The Plant Cell · doi:10.1105/tpc.112.098624 · Cited by 157
Iron homeostasis—Achilles’ heel of Aspergillus fumigatus?
Schrettl, M., & Haas, H. (2011) · Current Opinion in Microbiology · doi:10.1016/j.mib.2011.06.002 · Cited by 139
Fungal iron homeostasis with a focus on Aspergillus fumigatus
Misslinger, M., Hortschansky, P., Brakhage, A. A., & Haas, H. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2020.118885 · Cited by 137
Trejo-Hernández, A., Andrade-Domínguez, A., Hernández, M., & Encarnación, S. (2014) · The ISME Journal · doi:10.1038/ismej.2014.53 · Cited by 135
Gsaller, F., Hortschansky, P., Beattie, S. R., Klammer, V., Tuppatsch, K., Lechner, B. E., Rietzschel, N., Werner, E. R., Vogan, A. A., Chung, D., et al. (2014) · The EMBO Journal · doi:10.15252/embj.201489468 · Cited by 137
Gsaller, F., Hortschansky, P., Furukawa, T., Carr, P. D., Rash, B. M., Capilla, J., Müller, C., Bracher, F., Bowyer, P., Haas, H., et al. (2016) · PLoS Pathogens · doi:10.1371/journal.ppat.1005775 · Cited by 135
Lin, M.-F., Lin, Y.-Y., Yeh, H.-W., & Lan, C. (2014) · BMC Microbiology · doi:10.1186/1471-2180-14-119 · Cited by 124
Self-citationSingh, R. P., Prasad, H. K., Sinha, I., Agarwal, N., & Natarajan, K. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.233569 · Cited by 113
Divergent Targets of Candida albicans Biofilm Regulator Bcr1 In Vitro and In Vivo
Fanning, S., Xu, W., Solis, N., Woolford, C. A., Filler, S. G., & Mitchell, A. P. (2012) · Eukaryotic Cell · doi:10.1128/ec.00103-12 · Cited by 106
Candida albicans specializations for iron homeostasis: from commensalism to virulence
Noble, S. M. (2013) · Current Opinion in Microbiology · doi:10.1016/j.mib.2013.09.006 · Cited by 104
Yeast AP-1 like transcription factors (Yap) and stress response: a current overview
Rodrigues‐Pousada, C., Devaux, F., Caetano, S. M., Pimentel, C., da Silva, S. M., Gaspar‐Cordeiro, A., & Amaral, C. (2019) · Microbial Cell · doi:10.15698/mic2019.06.679 · Cited by 112
Johnson, L. J., Koulman, A., Christensen, M. J., Lane, G. A., Fraser, K., Forester, N. T., Johnson, R. D., Bryan, G. T., & Rasmussen, S. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003332 · Cited by 106
Conserved and Divergent Roles of Bcr1 and CFEM Proteins in Candida parapsilosis and Candida albicans
Ding, C., Vidanes, G. M., Maguire, S. L., Guida, A., Synnott, J. M., Andes, D. R., & Butler, G. (2011) · PLoS ONE · doi:10.1371/journal.pone.0028151 · Cited by 93
Sequence and Analysis of the Genome of the Pathogenic Yeast Candida orthopsilosis
Riccombeni, A., Vidanes, G. M., Proux‐Wéra, E., Wolfe, K. H., & Butler, G. (2012) · PLoS ONE · doi:10.1371/journal.pone.0035750 · Cited by 86
Lev, S., Desmarini, D., Chayakulkeeree, M., Sorrell, T. C., & Djordjevic, J. T. (2012) · PLoS ONE · doi:10.1371/journal.pone.0051403 · Cited by 85
Overview on the Bacterial Iron-Riboflavin Metabolic Axis
Cisternas, I. S., Salazar, J. C., & García-Angulo, V. A. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.01478 · Cited by 83
Verma, S., Shakya, V. P. S., & Idnurm, A. (2018) · Virulence · doi:10.1080/21505594.2017.1414133 · Cited by 67
Iron–sulfur cluster signaling: The common thread in fungal iron regulation
Gupta, M., & Outten, C. E. (2020) · Current Opinion in Chemical Biology · doi:10.1016/j.cbpa.2020.02.008 · Cited by 71
Chen, Y. Y., Chao, C., Liu, F., Hsu, P., Chen, H.-F., Peng, S.-C., Chuang, Y., Lan, C., Hsieh, W., & Wong, D. S. (2013) · PLoS ONE · doi:10.1371/journal.pone.0072483 · Cited by 65
Self-citationLapière, A., & Richard, M. L. (2022) · Gut Microbes · doi:10.1080/19490976.2022.2105610 · Cited by 61
Hwang, L. H., Seth, E. C., Gilmore, S. A., & Sil, A. (2011) · Eukaryotic Cell · doi:10.1128/ec.05274-11 · Cited by 63
Iron uptake and regulation in Schizosaccharomyces pombe
Labbé, S., Khan, M. G. M., & Jacques, J. (2013) · Current Opinion in Microbiology · doi:10.1016/j.mib.2013.07.007 · Cited by 61
The Monothiol Glutaredoxin Grx4 Regulates Iron Homeostasis and Virulence in Cryptococcus neoformans
Attarian, R., Hu, G., Caza, M., Sánchez‐León, E., Croll, D., Do, E., Bach, H., Missall, T. A., Lodge, J. K., Jung, W. H., et al. (2018) · mBio · doi:10.1128/mbio.02377-18 · Cited by 61
The Transcriptional Stress Response of Candida albicans to Weak Organic Acids
Cottier, F., Tan, A. S. M., Chen, J., Lum, J., Zolezzi, F., Poidinger, M., & Pavelka, N. (2015) · G3 Genes Genomes Genetics · doi:10.1534/g3.114.015941 · Cited by 57
The CCAAT-binding complex (CBC) in Aspergillus species
Hortschansky, P., Haas, H., Huber, E. M., Groll, M., & Brakhage, A. A. (2016) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2016.11.008 · Cited by 56
The Hap Complex in Yeasts: Structure, Assembly Mode, and Gene Regulation
Mao, Y., & Chen, C. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.01645 · Cited by 53
Amorim-Vaz, S., Delarze, E., Ischer, F., Sanglard, D., & Coste, A. T. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.00367 · Cited by 57
Study of Candida albicans and its interactions with the host: A mini review
Tsai, P.-W., Chen, Y.-T., Hsu, P., & Lan, C. (2013) · Biomedicine · doi:10.1016/j.biomed.2012.12.004 · Cited by 53
Self-citationTranscriptional Circuits Regulating Developmental Processes in Candida albicans
Rodríguez, D. L., Quail, M. M., Hernday, A. D., & Nobile, C. J. (2020) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.605711 · Cited by 55
Strategies of intracellular pathogens for obtaining iron from the environment
Leon-Sicairos, N., Reyes-Cortes, R., Guadrón-Llanos, A. M., Madueña-Molina, J., Leon-Sicairos, C., & Canizalez-Román, A. (2015) · BioMed Research International · doi:10.1155/2015/476534 · Cited by 51
Vandeputte, P., Pradervand, S., Ischer, F., Coste, A. T., Ferrari, S., Harshman, K., & Sanglard, D. (2012) · Eukaryotic Cell · doi:10.1128/ec.00134-12 · Cited by 51
Dual transcriptome of the immediate neutrophil and Candida albicans interplay
Niemiec, M. J., Grumaz, C., Ermert, D., Desel, C., Shankar, M., Lopes, J. P., Mills, I. G., Stevens, P., Sohn, K., & Urban, C. F. (2017) · BMC Genomics · doi:10.1186/s12864-017-4097-4 · Cited by 48
A novel hybrid iron regulation network combines features from pathogenic and nonpathogenic yeasts
Gerwien, F., Safyan, A., Wisgott, S., Hille, F., Kaemmer, P., Linde, J., Brunke, S., Kasper, L., & Hube, B. (2016) · mBio · doi:10.1128/mbio.01782-16 · Cited by 47
Xu, N., Dong, Y., Cheng, X., Yu, Q., Qian, K., Mao, J., Jia, C., Ding, X., Zhang, B., Chen, Y., et al. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2013.12.009 · Cited by 50
Merhej, J., Delaveau, T., Guitard, J., Palancade, B., Hennequin, C., Garcia, M., Lelandais, G., & Devaux, F. (2015) · Molecular Microbiology · doi:10.1111/mmi.12983 · Cited by 46
Xu, N., Qian, K., Dong, Y., Chen, Y., Yu, Q., Zhang, B., Xing, L., & Li, M. (2014) · Research in Microbiology · doi:10.1016/j.resmic.2014.03.001 · Cited by 44
The Monothiol Glutaredoxin Grx4 Exerts an Iron-Dependent Inhibitory Effect on Php4 Function
Vachon, P., Mercier, A., Jbel, M., & Labbé, S. (2012) · Eukaryotic Cell · doi:10.1128/ec.00060-12 · Cited by 44
Wang, Y., Deng, C., Tian, L., Xiong, D., Tian, C., & Klosterman, S. J. (2018) · mSphere · doi:10.1128/msphere.00400-18 · Cited by 46
Role of SFP1 in the Regulation of Candida albicans Biofilm Formation
Chen, H., & Lan, C. (2015) · PLoS ONE · doi:10.1371/journal.pone.0129903 · Cited by 46
Self-citationNovel insight into the expression and function of the multicopper oxidases in Candida albicans
Cheng, X., Xu, N., Yu, Q., Ding, X., Qian, K., Zhao, Q., Wang, Y., Zhang, B., Xing, L., & Li, M. (2013) · Microbiology · doi:10.1099/mic.0.065268-0 · Cited by 41
Hsu, C.-M., Liao, Y.-L., Chang, C.-K., & Lan, C. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221910633 · Cited by 40
Self-citationFurukawa, T., Scheven, M. T., Misslinger, M., Zhao, C., Hoefgen, S., Gsaller, F., Lau, J., Jöchl, C., Donaldson, I. J., Valiante, V., et al. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa109 · Cited by 40
Kaba, H. E., Nimtz, M., Müller, P. P., & Bilitewski, U. (2013) · BMC Microbiology · doi:10.1186/1471-2180-13-16 · Cited by 37
“Hap43p i s a transcription factor that is activated under low iron conditions and represses the xpr ssion of Sfu1p and of iron utilization genes so that repression of genes involved in iron uptake is relieved and the limited amount of iron is efficiently used for vital proteins [24].”
BackgroundHortschansky, P., Ando, E., Tuppatsch, K., Arikawa, H., Kobayashi, T., Kato, M., Haas, H., & Brakhage, A. A. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.628677 · Cited by 37
Molecular basis of the regulation of iron homeostasis in fission and filamentous yeasts
Brault, A., Mourer, T., & Labbé, S. (2015) · IUBMB Life · doi:10.1002/iub.1441 · Cited by 40
Iron‐responsive chromatin remodelling and MAPK signalling enhance adhesion in Candida albicans
Puri, S., Lai, W. K. M., Rizzo, J. M., Buck, M. J., & Edgerton, M. (2014) · Molecular Microbiology · doi:10.1111/mmi.12659 · Cited by 35
A network of paralogous stress response transcription factors in the human pathogen Candida glabrata
Merhej, J., Thiebaut, A., Blugeon, C., Pouch, J., Ali Chaouche, M. E. A., Camadro, J.-M., Le Crom, S., Lelandais, G., & Devaux, F. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00645 · Cited by 36
Aspergillus fumigatusvirulence through the lens of transcription factors: Table 1.
Bultman, K. M., Kowalski, C. H., & Cramer, R. A. (2016) · Medical Mycology · doi:10.1093/mmy/myw120 · Cited by 37
Heterologous Hsp90 promotes phenotypic diversity through network evolution
Koubková-Yu, T. C.-T., Chao, J.-C., & Leu, J. (2018) · PLoS Biology · doi:10.1371/journal.pbio.2006450 · Cited by 35
Lin, C., Lin, C.-N., Wang, Y., Liu, F.-Y., Chien, Y.-W., Chuang, Y., Lan, C., Hsieh, W., & Chen, B.-S. (2014) · BMC Systems Biology · doi:10.1186/1752-0509-8-s5-s6 · Cited by 36
Self-citationGerwien, F., Safyan, A., Wisgott, S., Brunke, S., Kasper, L., & Hube, B. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01055 · Cited by 33
Symeonidis, A. S., & Marangos, M. N. (2012) · InTech eBooks · doi:10.5772/34760 · Cited by 34
Environmental responses and the control of iron homeostasis in fungal systems
Canessa, P., & Larrondo, L. F. (2012) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-012-4615-x · Cited by 33
Pais, P., Costa, C., Cavalheiro, M., Romão, D., & Teixeira, M. C. (2016) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2016.00131 · Cited by 34
Connecting iron regulation and mitochondrial function in Cryptococcus neoformans
Horianopoulos, L. C., & Kronstad, J. W. (2019) · Current Opinion in Microbiology · doi:10.1016/j.mib.2019.04.002 · Cited by 32
Do, E., Cho, Y., Kim, D., Kronstad, J. W., & Jung, W. H. (2020) · Genetics · doi:10.1534/genetics.120.303270 · Cited by 34
Regulators of commensal and pathogenic life‐styles of an opportunistic fungus— Candida albicans
Rai, L. S., van Wijlick, L., Bougnoux, M., Bachellier‐Bassi, S., & d’Enfert, C. (2021) · Yeast · doi:10.1002/yea.3550 · Cited by 40
Coordination of hypoxia adaptation and iron homeostasis in human pathogenic fungi
Chung, D., Haas, H., & Cramer, R. A. (2012) · Frontiers in Microbiology · doi:10.3389/fmicb.2012.00381 · Cited by 29
The tug-of-war on iron between plant and pathogen
Sun, J., Xiao, S., & Xue, C. (2023) · Phytopathology Research · doi:10.1186/s42483-023-00215-8 · Cited by 28
The regulation of iron homeostasis in the fungal human pathogen Candida glabrata
Devaux, F., & Thiébaut, A. (2019) · Microbiology · doi:10.1099/mic.0.000807 · Cited by 29
Jia, C., Zhang, K., Yu, Q., Zhang, B., Xiao, C., Dong, Y., Chen, Y., Zhang, B., Xing, L., & Li, M. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2015.08.005 · Cited by 26
Thiébaut, A., Delaveau, T., Benchouaia, M., Boeri, J., Garcia, M., Lelandais, G., & Devaux, F. (2017) · Scientific Reports · doi:10.1038/s41598-017-03750-5 · Cited by 29
Duval, C., Macabiou, C., Garcia, C., Lesuisse, E., Camadro, J., & Auchère, F. (2019) · MicrobiologyOpen · doi:10.1002/mbo3.970 · Cited by 25
Palmieri, D., Segorbe, D., López‐Berges, M. S., Curtis, F. D., Lima, G., Pietro, A. D., & Turrà, D. (2023) · Toxins · doi:10.3390/toxins15010050 · Cited by 25
Chakravarti, A., Camp, K., McNabb, D. S., & Pinto, I. (2017) · PLOS ONE · doi:10.1371/journal.pone.0170649 · Cited by 24
Xu, N., Cheng, X., Yu, Q., Qian, K., Ding, X., Liu, R., Zhang, B., Xing, L., & Li, M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0062367 · Cited by 24
Chen, Y.-T., Lin, C.-Y., Tsai, P.-W., Yang, C., Hsieh, W., & Lan, C. (2011) · Eukaryotic Cell · doi:10.1128/ec.05200-11 · Cited by 25
Self-citationPhp4 Is a Key Player for Iron Economy in Meiotic and Sporulating Cells
Brault, A., Rallis, C., Normant, V., Garant, J., Bähler, J., & Labbé, S. (2016) · G3 Genes Genomes Genetics · doi:10.1534/g3.116.031898 · Cited by 28
Candida albicans Aro1 affects cell wall integrity, biofilm formation and virulence
Yeh, Y.-C., Wang, H.-Y., & Lan, C. (2018) · Journal of Microbiology Immunology and Infection · doi:10.1016/j.jmii.2018.04.002 · Cited by 23
Self-citationBiosynthesis of Vitamin B2 and Flavocoenzymes in Plants
Fischer, M. J., & Bacher, A. (2011) · Advances in botanical research · doi:10.1016/b978-0-12-386479-6.00003-2 · Cited by 22
Lee, H., Chao, J.-C., Cheng, K.-Y., & Leu, J. (2018) · Journal of Cell Science · doi:10.1242/jcs.220202 · Cited by 21
Alkafeef, S. S., Lane, S., Yu, C., Zhou, T., Solis, N. V., Filler, S. G., Huang, L., & Liu, H. (2020) · PLoS Genetics · doi:10.1371/journal.pgen.1008881 · Cited by 22
Candida albicans Hap43 Domains Are Required under Iron Starvation but Not Excess
Skrahina, V., Brock, M., Hube, B., & Brunke, S. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.02388 · Cited by 23
López‐Berges, M. S., Scheven, M. T., Hortschansky, P., Misslinger, M., Baldin, C., Gsaller, F., Werner, E. R., Krüger, T., Kniemeyer, O., Weber, J., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22147739 · Cited by 21
Iron acquisition in the human fungal pathogen Cryptococcus neoformans
Jung, W. H., & Do, E. (2013) · Current Opinion in Microbiology · doi:10.1016/j.mib.2013.07.008 · Cited by 18
Deciphering the oxidative stress response in Candida albicans
Arribas, V., Gil, C., & Molero, G. (2025) · Fungal Biology Reviews · doi:10.1016/j.fbr.2025.100427 · Cited by 20
Aoki, W., Tatsukami, Y., Kitahara, N., Matsui, K., Morisaka, H., Kuroda, K., & Ueda, M. (2013) · Journal of Proteomics · doi:10.1016/j.jprot.2013.07.031 · Cited by 18
Diverse Hap43-Independent Functions of the Candida albicans CCAAT-Binding Complex
Hsu, P., Chao, C., Yang, C., Ye, Y.-L., Liu, F., Chuang, Y., & Lan, C. (2013) · Eukaryotic Cell · doi:10.1128/ec.00014-13 · Cited by 18
Self-citationJung, W. H., Sánchez‐León, E., & Kronstad, J. W. (2021) · Current Genetics · doi:10.1007/s00294-021-01172-5 · Cited by 18
Proteotoxicity caused by perturbed protein complexes underlies hybrid incompatibility in yeast
Swamy, K. B. S., Lee, H., Ladra, C., Liu, C.-F. J., Chao, J.-C., Chen, Y.-Y., & Leu, J. (2022) · Nature Communications · doi:10.1038/s41467-022-32107-4 · Cited by 18
Marquez, L., Lee, Y., Duncan, D., Whitesell, L. J., Cowen, L. E., & Quave, C. L. (2023) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.3c00113 · Cited by 17
Kröber, A., Scherlach, K., Hortschansky, P., Shelest, E., Staib, P., Kniemeyer, O., & Brakhage, A. A. (2016) · PLoS ONE · doi:10.1371/journal.pone.0150701 · Cited by 19
Li, J., Zhang, C., Huang, X., Sun, H., Yang, L., Liu, H., Zhang, L., Wu, N., Xie, Y., Qi, J., et al. (2026) · Cancer Cell · doi:10.1016/j.ccell.2026.02.001 · Cited by 19
Iron competition in fungus-plant interactions
López‐Berges, M. S., Turrà, D., Capilla, J., Schafferer, L., Matthijs, S., Jöchl, C., Cornélis, P., Guarro, J., Haas, H., & Pietro, A. D. (2013) · Plant Signaling & Behavior · doi:10.4161/psb.23012 · Cited by 16
Zhang, D., Dong, Y., Yu, Q., Zhang, K., Zhang, M., Jia, C., Xiao, C., Zhang, B., Zhang, B., & Li, M. (2017) · Future Microbiology · doi:10.2217/fmb-2017-0098 · Cited by 16
Candida albicans adds more weight to iron regulation
Blankenship, J. R., & Mitchell, A. P. (2011) · Cell Host & Microbe · doi:10.1016/j.chom.2011.08.001 · Cited by 15
HapX-mediated H2B deub1 and SreA-mediated H2A.Z deposition coordinate in fungal iron resistance
Sun, K., Li, Y., Gai, Y., Wang, J., Jian, Y., Liu, X., Wu, L., Shim, W., Lee, Y., Ma, Z., et al. (2023) · Nucleic Acids Research · doi:10.1093/nar/gkad708 · Cited by 15
Jiang, Q., Deng, Y., Li, S., Yang, D., & Li, T. (2023) · Journal of Oral Microbiology · doi:10.1080/20002297.2023.2278937 · Cited by 15
Prokopiv, T., Fedorovych, D. V., Boretsky, Y. R., & Sibirny, A. А. (2012) · Current Microbiology · doi:10.1007/s00284-012-0242-0 · Cited by 15
Experimental evolution reveals a general role for the methyltransferase Hmt1 in noise buffering
You, S., Jhou, Y., Kao, C.-F., & Leu, J. (2019) · PLoS Biology · doi:10.1371/journal.pbio.3000433 · Cited by 15
Metal Acquisition and Homeostasis in Fungi
Bailão, E. F. L. C., Parente, A. F. A., Parente, J. A., Bailão, M. G. S., de Castro, K. P., Kmetzsch, L., Staats, C. C., Schrank, A., Vainstein, M. H., Borges, C. L., et al. (2012) · Current Fungal Infection Reports · doi:10.1007/s12281-012-0108-8 · Cited by 15
Fungal NRPS-Dependent Siderophores: From Function to Prediction
Sørensen, J. L., Knudsen, M., Hansen, F. T., Olesen, C., Fuertes, P. R., Lee, T. V., Søndergaard, T. E., Pedersen, C. N. S., Brodersen, D. E., & Giese, H. (2014) · Fungal biology · doi:10.1007/978-1-4939-1191-2_15 · Cited by 14
The role of Mss11 in Candida albicans biofilm formation
Tsai, P.-W., Chen, Y.-T., Yang, C., Chen, H.-F., Tan, T.-S., Lin, T.-W., Hsieh, W., & Lan, C. (2014) · Molecular Genetics and Genomics · doi:10.1007/s00438-014-0846-0 · Cited by 13
Self-citationCandida albicans Hom6 is a homoserine dehydrogenase involved in protein synthesis and cell adhesion
Tsai, P.-W., Chien, C.-Y., Yeh, Y.-C., Tung, L., Chen, H., Chang, T., & Lan, C. (2016) · Journal of Microbiology Immunology and Infection · doi:10.1016/j.jmii.2016.03.001 · Cited by 13
Self-citationArribas, V., Monteoliva, L., Hernáez, M. L., Gil, C., & Molero, G. (2024) · Antioxidants · doi:10.3390/antiox13050527 · Cited by 12
Metadata
- Authors
- Hsu, P.-C., Yang, C.-Y., & Lan, C.-Y.
- Affiliations
- Institute of Molecular and Cellular Biology, No. 101, Section 2, Kuang Fu Road, Hsinchu 30013, Taiwan, Republic of China
- Animal Technology Institute Taiwan (TW)
- National Tsing Hua University (TW)
- Corresponding author
- Lan, Chung-Yu
- Venue
- Eukaryotic Cell
- Publisher
- American Society for Microbiology
- Published
- 2011-02
- Volume
- 10
- Issue
- 2
- Pages
- 207-225
- ISSN
- 1535-9778 (ISSN-L)
- 1535-9786
- PMC
- PMC3067405
- OpenAlex
- W2146920262
- Cited by
- 157
- References
- 94
- Citations by year
- 2026: 4 · 2025: 11 · 2024: 10 · 2023: 10 · 2022: 8 · 2021: 10 · 2020: 8 · 2019: 9 · 2018: 9 · 2017: 10 · 2016: 10 · 2015: 8 · 2014: 13 · 2013: 14 · 2012: 14
- FWCI
- 4.82
- Type
- journal article
- Language
- en
- Open access
- diamond
- doi.org
- Locations
- Eukaryotic Cell (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
- Health Sciences › Medicine › Infectious Diseases › Fungal Infections and Studies
- Keywords
- Candida albicans, iron starvation, Tup1, iron acquisition, iron-sulfur cluster assembly, mitochondrial respiration, fungal virulence, natural resistance to infection, transcriptional repressor
- MeSH terms
- Iron Deficiencies, Amino Acid Sequence, Animals, Candida albicans, Candidiasis, Cell Nucleus, Female, Flavins, Fungal Proteins, Humans, Iron, Kidney, Mice, Inbred BALB C, Molecular Sequence Data, Repressor Proteins, Virulence, Gene Expression Regulation, Fungal, Sequence Alignment, Gene Deletion, Sequence Homology, Amino Acid, Two-Hybrid System Techniques, Cell Proliferation, Mice
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