Gene Essentiality Analyzed by In Vivo Transposon Mutagenesis and Machine Learning in a Stable Haploid Isolate of Candida albicans
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Comprehensive understanding of an organism requires that we understand the contributions of most, if not all, of its genes. Classical genetic approaches to this issue have involved systematic deletion of each gene in the genome, with comprehensive sets of mutants available only for very-well-studied model organisms. We took a different approach, harnessing the power of in vivo transposition coupled with deep sequencing to identify >500,000 different mutations, one per cell, in the prevalent human fungal pathogen Candida albicans and to map their positions across the genome. The transposition approach is efficient and less labor-intensive than classic approaches. Here, we describe the production and analysis (aided by machine learning) of a large collection of mutants and the comprehensive identification of 1,610 C. albicans genes that are essential for growth under standard laboratory conditions. Among these C. albicans essential genes, we identify those that are also essential in two distantly related model yeasts as well as those that are conserved in all four major human fungal pathogens and that are not conserved in the human genome. This list of genes with functions important for the survival of the pathogen provides a good starting point for the development of new antifungal drugs, which are greatly needed because of the emergence of fungal pathogens with elevated resistance and/or tolerance of the currently limited set of available antifungal drugs.
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In several fungal species, including S. cerevisiae and C. albicans, it is estimated that ∼20% of open reading frames are essential.
“In several fungal species, including the model yeast Saccharomyces cerevisiae and the distantly related fungal pathogen C. albicans, it is estimated that ∼20% of the open reading frames in their genomes are essential (Winzeler et al. 1999; Segal et al. 2018).”
From Genetic analysis of Hsp90 function in <i>Cryptococcus neoformans</i> highlights key roles in stress tolerance and virulence (2022) · cites this paper as Segal et al. 2018
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Cites
Breiman, L. (2001) · Machine Learning · doi:10.1023/a:1010933404324 · Cited by 133,538 · see citing works
Scikit-learn: Machine Learning in Python
Pedregosa, F., Varoquaux, G., Gramfort, A., Michel, V., Thirion, B., Grisel, O., Blondel, M., Müller, A., Nothman, J., Louppe, G., et al. (2012) · arXiv · doi:10.48550/arxiv.1201.0490 · Cited by 71,016 · see citing works
The Sequence Alignment/Map format and SAMtools
Li, H., Handsaker, B., Wysoker, A., Fennell, T., Ruan, J., Homer, N., Marth, G., Abecasis, G., Durbin, R., & 1000 Genome Project Data Processing Subgroup (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp352 · Cited by 62,041 · see citing works
Fast gapped-read alignment with Bowtie 2
Langmead, B., & Salzberg, S. L. (2012) · Nature Methods · doi:10.1038/nmeth.1923 · Cited by 56,400 · see citing works
Cutadapt removes adapter sequences from high-throughput sequencing reads
Martin, M. (2011) · EMBnet.journal · doi:10.14806/ej.17.1.200 · Cited by 33,889 · see citing works
Classification And Regression Trees
Breiman, L., Friedman, J. H., Olshen, R. A., & Stone, C. J. (2017) · doi:10.1201/9781315139470 · Cited by 11,417 · see citing works
Database resources of the National Center for Biotechnology Information: update
Wheeler, D. L. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkh073 · Cited by 10,691 · see citing works
Database resources of the National Center for Biotechnology Information
Agarwala, R., Barrett, T., Beck, J., Benson, D., Bollin, C., Bolton, E. E., Bourexis, D., Brister, J., Bryant, S. H., Canese, K., et al. (2017) · Nucleic Acids Res. · doi:10.1093/nar/gkx1095 · Cited by 6,277 · see citing works
Current protocols in molecular biology
Dudley, R. K. (1988) · FEBS Letters · doi:10.1016/0014-5793(88)80264-3 · Cited by 6,037 · see citing works
NWChem: A comprehensive and scalable open-source solution for large scale molecular simulations
Valiev, M., Bylaska, E. J., Govind, N., Kowalski, K., Straatsma, T. P., van Dam, H. J. J., Wang, D., Nieplocha, J., Aprà, E., Windus, T. L., et al. (2010) · Computer Physics Communications · doi:10.1016/j.cpc.2010.04.018 · Cited by 5,794 · see citing works
Functional profiling of the Saccharomyces cerevisiae genome
Giaever, G., Chu, A. M., Ni, L., Connelly, C., Riles, L., Véronneau, S., Dow, S., Lucau-Danila, A., Anderson, K., André, B., et al. (2002) · Nature · doi:10.1038/nature00935 · Cited by 4,316 · see citing works
Hidden Killers: Human Fungal Infections
Brown, G. D., Denning, D. W., Gow, N. A. R., Levitz, S. M., Netea, M. G., & White, T. C. (2012) · Science Translational Medicine · doi:10.1126/scitranslmed.3004404 · Cited by 4,284 · see citing works
Self-citationCurrent protocols in molecular biology
(1988) · Trends in Biochemical Sciences · doi:10.1016/0968-0004(88)90131-4 · Cited by 4,234 · see citing works
Winzeler, E. A., Shoemaker, D. D., Astromoff, A., Liang, H., Anderson, K., Andre, B., Bangham, R., Benito, R., Boeke, J. D., Bussey, H., et al. (1999) · Science · doi:10.1126/science.285.5429.901 · Cited by 3,953 · see citing works
Hoffman, C. S., & Winston, F. (1987) · Gene · doi:10.1016/0378-1119(87)90131-4 · Cited by 2,492 · see citing works
Saccharomyces Genome Database: the genomics resource of budding yeast
Cherry, J., Hong, E., Amundsen, C., Balakrishnan, R., Binkley, G., Chan, E. T., Christie, K., Costanzo, M., Dwight, S., Engel, S., et al. (2011) · Nucleic Acids Res. · doi:10.1093/nar/gkr1029 · Cited by 1,886 · see citing works
Methods in yeast genetics : a Cold Spring Harbor Laboratory course manual
Amberg, D. C., Burke, D. J., & Strathern, J. N. (2005) · Cited by 1,853 · see citing works
The origin and behavior of mutable loci in maize
McClintock, B. (1950) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.36.6.344 · Cited by 1,752 · see citing works
The genome sequence of Schizosaccharomyces pombe
Wood, V., Gwilliam, R., Rajandream, M.-A., Lyne, M. H., Lyne, R., Stewart, A., SGOUROS, J. G., Peat, N., Hayles, J., Baker, S. G., et al. (2002) · Nature · doi:10.1038/nature724 · Cited by 1,650 · see citing works
Kullberg, B. J., & Arendrup, M. C. (2015) · New England Journal of Medicine · doi:10.1056/nejmra1315399 · Cited by 1,315 · see citing works
A global genetic interaction network maps a wiring diagram of cellular function
Costanzo, M., VanderSluis, B., Koch, E. N., Baryshnikova, A., Pons, C., Tan, G., Wang, W., Usaj, M., Hanchard, J., Lee, S. D., et al. (2016) · Science · doi:10.1126/science.aaf1420 · Cited by 1,240 · see citing works
Griffin, J. E., Gawronski, J. D., DeJesus, M. A., Ioerger, T. R., Akerley, B. J., & Sassetti, C. M. (2011) · PLoS Pathogens · doi:10.1371/journal.ppat.1002251 · Cited by 1,048 · see citing works
An Introduction to Sequence Similarity (“Homology”) Searching
Pearson, W. R. (2013) · Current Protocols in Bioinformatics · doi:10.1002/0471250953.bi0301s42 · Cited by 946 · see citing works
van Opijnen, T., Bodi, K. L., & Camilli, A. (2009) · Nature Methods · doi:10.1038/nmeth.1377 · Cited by 926 · see citing works
Analysis of a genome-wide set of gene deletions in the fission yeast Schizosaccharomyces pombe
Kim, D.-U., Hayles, J., Kim, D., Wood, V., Park, H.-O., Won, M., Yoo, H.-S., Duhig, T., Nam, M., Palmer, G., et al. (2010) · Nature Biotechnology · doi:10.1038/nbt.1628 · Cited by 742 · see citing works
Byrne, K. P., & Wolfe, K. H. (2005) · Genome Research · doi:10.1101/gr.3672305 · Cited by 720 · see citing works
Noble, S. M., French, S., Kohn, L. A., Chen, V., & Johnson, A. D. (2010) · Nature Genetics · doi:10.1038/ng.605 · Cited by 678 · see citing works
Simultaneous assay of every Salmonella Typhi gene using one million transposon mutantsPreprint
Langridge, G. C., Phan, M., Turner, D., Perkins, T. T., Parts, L., Haase, J. K., Charles, I. G., Maskell, D. J., Peters, S. E., Gordon Dougan, B., et al. (2009) · Genome Research · doi:10.1101/gr.097097.109 · Cited by 618 · see citing works
Mutant phenotypes for thousands of bacterial genes of unknown function
Price, M. N., Wetmore, K. M., Waters, R. J., Callaghan, M., Ray, J., Liu, H., Kuehl, J. V., Melnyk, R. A., Lamson, J. S., Suh, Y., et al. (2018) · Nature · doi:10.1038/s41586-018-0124-0 · Cited by 576 · see citing works
The BLAST Sequence Analysis Tool
Madden, T. (2013) · Cited by 535 · see citing works
Roemer, T., Jiang, B., Davison, J., Ketela, T. W., Veillette, K., Breton, A., Tandia, F., Linteau, A., Sillaots, S., Marta, C., et al. (2003) · Molecular Microbiology · doi:10.1046/j.1365-2958.2003.03697.x · Cited by 513 · see citing works
Transposon insertion sequencing: a new tool for systems-level analysis of microorganisms
van Opijnen, T., & Camilli, A. (2013) · Nature Reviews Microbiology · doi:10.1038/nrmicro3033 · Cited by 495 · see citing works
How to bolster the antifungal pipeline
Denning, D. W., & Bromley, M. (2015) · Science · doi:10.1126/science.aaa6097 · Cited by 481 · see citing works
Skrzypek, M. S., Binkley, J., Binkley, G., Miyasato, S. R., Simison, M., & Sherlock, G. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkw924 · Cited by 455 · see citing works
A Phenotypic Profile of the Candida albicans Regulatory Network
Homann, O. R., Dea, J., Noble, S. M., & Johnson, A. D. (2009) · PLoS Genetics · doi:10.1371/journal.pgen.1000783 · Cited by 444 · see citing works
The Reference Genome Sequence ofSaccharomyces cerevisiae: Then and Now
Engel, S. R., Dietrich, F. S., Fisk, D. G., Binkley, G., Balakrishnan, R., Costanzo, M. C., Dwight, S. S., Hitz, B. C., Karra, K., Nash, R. S., et al. (2014) · G3 Genes Genomes Genetics · doi:10.1534/g3.113.008995 · Cited by 428 · see citing works
Genotype to Phenotype: A Complex Problem
Dowell, R. D., Ryan, O. W., Jansen, A., Cheung, D., Agarwala, S. D., Danford, T., Bernstein, D. A., Rolfe, A., Heisler, L. E., Chin, B., et al. (2010) · Science · doi:10.1126/science.1189015 · Cited by 408 · see citing works
Quantitative analysis of fitness and genetic interactions in yeast on a genome scale
Baryshnikova, A., Costanzo, M., Kim, Y., Ding, H., Koh, J., Toufighi, K., Youn, J.-Y., Ou, J., San Luis, B.-J., Bandyopadhyay, S., et al. (2010) · Nature Methods · doi:10.1038/nmeth.1534 · Cited by 364 · see citing works
A Candida albicans CRISPR system permits genetic engineering of essential genes and gene families
Vyas, V. K., Barrasa, M. I., & Fink, G. R. (2015) · Science Advances · doi:10.1126/sciadv.1500248 · Cited by 363 · see citing works
Isolation of quiescent and nonquiescent cells from yeast stationary-phase cultures
Allen, C., Büttner, S., Aragon, A. D., Thomas, J., Meirelles, O., Jaetao, J. E., Benn, D., Ruby, S. W., Marten Veenhuis, A., Madeo, F., et al. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200604072 · Cited by 338 · see citing works
PomBase: a comprehensive online resource for fission yeast
Wood, V., Harris, M. A., McDowall, M. D., Rutherford, K., Vaughan, B. W., Staines, D. M., Aslett, M., Lock, A., Bahler, J., Kersey, P. J., et al. (2012) · Nucleic Acids Research · doi:10.1093/nar/gkr853 · Cited by 321 · see citing works
Rewiring of the Yeast Transcriptional Network Through the Evolution of Motif Usage
Ihmels, J., Bergmann, S., Gerami‐Nejad, M., Yanai, I., McClellan, M., Berman, J. G., & Barkai, N. (2005) · Science · doi:10.1126/science.1113833 · Cited by 295 · see citing works
Self-citationThe ‘obligate diploid’ Candida albicans forms mating-competent haploids
Hickman, M. A., Zeng, G., Forche, A., Hirakawa, M. P., Abbey, D., Harrison, B. D., Wang, Y.-M., Su, C.-H., Bennett, R. J., Wang, Y., et al. (2013) · Nature · doi:10.1038/nature11865 · Cited by 284 · see citing works
Self-citationThe art and design of genetic screens: yeast
Forsburg, S. L. (2001) · Nature Reviews Genetics · doi:10.1038/35088500 · Cited by 260 · see citing works
Genome-Wide Fitness Test and Mechanism-of-Action Studies of Inhibitory Compounds in Candida albicans
Xu, D., Jiang, B., Ketela, T. W., Lemieux, S., Veillette, K., Martel, N., Davison, J., Sillaots, S., Trosok, S., Bachewich, C., et al. (2007) · PLoS Pathogens · doi:10.1371/journal.ppat.0030092 · Cited by 249 · see citing works
Candida albicans Gene Deletion with a Transient CRISPR-Cas9 System
Min, K., Ichikawa, Y., Woolford, C. A., & Mitchell, A. P. (2016) · mSphere · doi:10.1128/msphere.00130-16 · Cited by 246 · see citing works
Where does fission yeast sit on the tree of life?
Sipiczki, M. (2000) · Genome biology · doi:10.1186/gb-2000-1-2-reviews1011 · Cited by 243 · see citing works
Global analysis of fungal morphology exposes mechanisms of host cell escape
O’Meara, T. R., Veri, A. O., Ketela, T., Jiang, B., Roemer, T., & Cowen, L. E. (2015) · Nature Communications · doi:10.1038/ncomms7741 · Cited by 243 · see citing works
A recyclableCandida albicans URA3 cassette for PCR product-directed gene disruptions
Wilson, R. B., Davis, D. A., Enloe, B. M., & Mitchell, A. P. (2000) · Yeast · doi:10.1002/(sici)1097-0061(20000115)16:1 · Cited by 228 · see citing works
The Role of Nucleosome Positioning in the Evolution of Gene Regulation
Tsankov, A. M., Thompson, D. A., Socha, A. L., Regev, A., & Rando, O. J. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000414 · Cited by 217 · see citing works
Global Gene Deletion Analysis Exploring Yeast Filamentous Growth
Ryan, O. W., Shapiro, R. S., Kurat, C. F., Mayhew, D. N., Baryshnikova, A., Chin, B., Lin, Z., Cox, M. J., Vizeacoumar, F. S., Cheung, D., et al. (2012) · Science · doi:10.1126/science.1224339 · Cited by 213 · see citing works
McEntyre, J. R., & Ostell, J. (2002) · Cited by 210 · see citing works
Bruno, V. M., Wang, Z., Marjani, S. L., Euskirchen, G. M., Martin, J. V., Sherlock, G. J., & Snyder, M. P. (2010) · Genome Research · doi:10.1101/gr.109553.110 · Cited by 210 · see citing works
Bromodomain factor 1 corresponds to a missing piece of yeast TFIIDPreprint
Matangkasombut, O., Buratowski, R. M., Swilling, N. W., & Buratowski, S. (2000) · Genes & Development · doi:10.1101/gad.14.8.951 · Cited by 203 · see citing works
One library to make them all: streamlining the creation of yeast libraries via a SWAp-Tag strategy
Yofe, I., Weill, U., Meurer, M., Chuartzman, S. G., Zalckvar, E., Goldman, O., Ben‐Dor, S., Schütze, C., Wiedemann, N., Knop, M., et al. (2016) · Nature Methods · doi:10.1038/nmeth.3795 · Cited by 202 · see citing works
Genome-wide Consequences of Deleting Any Single Gene
Teng, X., Dayhoff-Brannigan, M., Cheng, W., Gilbert, C. E., Sing, C. N., Diny, N. L., Wheelan, S. J., Dunham, M. J., Boeke, J. D., Pineda, F. J., et al. (2013) · Molecular Cell · doi:10.1016/j.molcel.2013.09.026 · Cited by 193 · see citing works
Uhl, M. A., Biery, M., Craig, N., & Johnson, A. D. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg256 · Cited by 191 · see citing works
McKee, A. H. Z., & Kleckner, N. E. (1997) · Genetics · doi:10.1093/genetics/146.3.797 · Cited by 189 · see citing works
Davis, D. A., Bruno, V. M., Loza, L., Filler, S. G., & Mitchell, A. P. (2002) · Genetics · doi:10.1093/genetics/162.4.1573 · Cited by 184 · see citing works
Hromatka, B. S., Noble, S. M., & Johnson, A. D. (2005) · Molecular Biology of the Cell · doi:10.1091/mbc.e05-05-0435 · Cited by 183 · see citing works
Chandler, C. H., Chari, S., & Dworkin, I. M. (2013) · Trends in Genetics · doi:10.1016/j.tig.2013.01.009 · Cited by 174 · see citing works
Genome-wide SWAp-tag yeast libraries for proteome exploration
Weill, U., Yofe, I., Sass, E., Stynen, B., Davidi, D., Natarajan, J., Ben-Menachem, R., Avihou, Z., Goldman, O., Harpaz, N., et al. (2018) · Nature Methods · doi:10.1038/s41592-018-0044-9 · Cited by 167 · see citing works
Functional mapping of yeast genomes by saturated transposition
Michel, A. H., Hatakeyama, R., Kimmig, P., Arter, M., Peter, M., Matos, J., VIRGILIO, C. D., & Kornmann, B. (2017) · eLife · doi:10.7554/elife.23570 · Cited by 155 · see citing works
A CRISPR–Cas9-based gene drive platform for genetic interaction analysis in Candida albicans
Shapiro, R. S., Chavez, A., Porter, C. B. M., Hamblin, M., Kaas, C. S., DiCarlo, J. E., Zeng, G., Xu, X., Revtovich, A. V., Kirienko, N. V., et al. (2017) · Nature Microbiology · doi:10.1038/s41564-017-0043-0 · Cited by 152 · see citing works
Backup without redundancy: genetic interactions reveal the cost of duplicate gene loss
Ihmels, J., Collins, S. R., Schuldiner, M., Krogan, N. J., & Weissman, J. S. (2007) · Molecular Systems Biology · doi:10.1038/msb4100127 · Cited by 151 · see citing works
Candida auris : An emerging multidrug-resistant pathogen
Sears, D., & Schwartz, B. S. (2017) · International Journal of Infectious Diseases · doi:10.1016/j.ijid.2017.08.017 · Cited by 146 · see citing works
An Efficient, Rapid, and Recyclable System for CRISPR-Mediated Genome Editing in Candida albicans
Nguyen, N., Quail, M. M., & Hernday, A. D. (2017) · mSphere · doi:10.1128/mspheredirect.00149-17 · Cited by 137 · see citing works
Pathway analysis of Candida albicans survival and virulence determinants in a murine infection model
Becker, J. M., Kauffman, S., Hauser, M., Huang, L.-Y., Lin, M. T.-Y., Sillaots, S., Jiang, B., Xu, D., & Roemer, T. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1009845107 · Cited by 135 · see citing works
Genome-Wide Distribution of TransposedDissociationElements in Maize
Vollbrecht, E., Duvick, J. P., Schares, J. A., Ahern, K. R., Deewatthanawong, P., Xu, L., Conrad, L. J., Kikuchi, K., Kubinec, T. A., Hall, B. D., et al. (2010) · The Plant Cell · doi:10.1105/tpc.109.073452 · Cited by 131 · see citing works
Shi, Q.-M., Wang, Y.-M., Zheng, X., Lee, R. T. H., & Wang, Y. (2006) · Molecular Biology of the Cell · doi:10.1091/mbc.e06-05-0442 · Cited by 124 · see citing works
Muzzey, D., Schwartz, K., Weissman, J. S., & Sherlock, G. (2013) · Genome biology · doi:10.1186/gb-2013-14-9-r97 · Cited by 123 · see citing works
The extensive and condition-dependent nature of epistasis among whole-genome duplicates in yeastPreprint
Musso, G. A., Costanzo, M., Huangfu, M., Smith, A. M., Paw, J., Luis, B.-J. S., Boone, C. M., Giaever, G. N., Nislow, C., Emili, A., et al. (2008) · Genome Research · doi:10.1101/gr.076174.108 · Cited by 121 · see citing works
Advanced Methods for High-Throughput Microscopy Screening of Genetically Modified Yeast Libraries
Cohen, Y., & Schuldiner, M. (2011) · Methods in molecular biology · doi:10.1007/978-1-61779-276-2_8 · Cited by 115 · see citing works
Richter, G., Fischer, M. J., Krieger, C., Eberhardt, S., Lüttgen, H., Schaaff‐Gerstenschläger, I., & Bacher, A. (1997) · Journal of Bacteriology · doi:10.1128/jb.179.6.2022-2028.1997 · Cited by 112 · see citing works
Bdf1, a Yeast Chromosomal Protein Required for Sporulation
Chua, P. R., & Roeder, G. S. (1995) · Molecular and Cellular Biology · doi:10.1128/mcb.15.7.3685 · Cited by 109 · see citing works
Transposition of maize Ac/Ds transposable elements in the yeast Saccharomyces cerevisiae
Weil, C. F., & Kunze, R. (2000) · Nature Genetics · doi:10.1038/82827 · Cited by 105 · see citing works
Self-citationDNA transposon Hermes inserts into DNA in nucleosome-free regions in vivo
Gangadharan, S., Mularoni, L., Fain-Thornton, J., Wheelan, S. J., & Craig, N. L. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1016382107 · Cited by 102 · see citing works
Oh, J., Fung, E., Schlecht, U., Davis, R. W., Giaever, G. N., St.Onge, R. P., Deutschbauer, A. M., & Nislow, C. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1001140 · Cited by 96 · see citing works
Padmanabhan, S., Thakur, J., Siddharthan, R., & Sanyal, K. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0809770105 · Cited by 87 · see citing works
Lygerou, Z., Conesa, C., Lesage, P., Swanson, R. N., Ruet, A., Carlson, M., Sentenac, A., & Séraphin, B. (1994) · Nucleic Acids Research · doi:10.1093/nar/22.24.5332 · Cited by 84 · see citing works
Gerami‐Nejad, M., Zacchi, L. F., McClellan, M., Matter, K. J., & Berman, J. G. (2013) · Microbiology · doi:10.1099/mic.0.064097-0 · Cited by 84 · see citing works
Self-citationThe G 1 Cyclin Cln3 Regulates Morphogenesis in Candida albicans
Chapa‐y‐Lazo, B., Bates, S., & Sudbery, P. E. (2005) · Eukaryotic Cell · doi:10.1128/ec.4.1.90-94.2005 · Cited by 80 · see citing works
Meir, Y. J., Weirauch, M. T., Yang, H.-S., Chung, P.-C., Yu, R. K., & Wu, S. C. (2011) · BMC Biotechnology · doi:10.1186/1472-6750-11-28 · Cited by 75 · see citing works
FYPO: the fission yeast phenotype ontology
Harris, M. A., Lock, A., Bähler, J., Oliver, S. G., & Wood, V. (2013) · Bioinformatics · doi:10.1093/bioinformatics/btt266 · Cited by 69 · see citing works
Vitamin Biosynthesis as an Antifungal Target
Meir, Z., & Osherov, N. (2018) · Journal of Fungi · doi:10.3390/jof4020072 · Cited by 69 · see citing works
Analysis of Candida albicans plasma membrane proteome
Cabezón, V., Llama‐Palacios, A., Nombela, C., Monteoliva, L., & Gil, C. (2009) · PROTEOMICS · doi:10.1002/pmic.200800988 · Cited by 62 · see citing works
Integration Profiling of Gene Function With Dense Maps of Transposon Integration
Guo, Y.-B., Park, J.-M., Cui, B.-W., Humes, E., Gangadharan, S., Hung, S., FitzGerald, P., Hoe, K.-L., Grewal, S., Craig, N., et al. (2013) · Genetics · doi:10.1534/genetics.113.152744 · Cited by 62 · see citing works
Large-Scale Gene Disruption Using the UAU1 Cassette
Nobile, C. J., & Mitchell, A. P. (2009) · Methods in molecular biology · doi:10.1007/978-1-60327-151-6_17 · Cited by 59 · see citing works
Generation of conditional lethal Candida albicans mutants by inducible deletion of essential genes
Michel, S., Ushinsky, S. C., Klebl, B., Leberer, E., Thomas, D. Y., Whiteway, M. S., & Morschhäuser, J. (2002) · Molecular Microbiology · doi:10.1046/j.1365-2958.2002.03167.x · Cited by 56 · see citing works
Vandeputte, P., Ischer, F., Sanglard, D., & Coste, A. T. (2011) · PLoS ONE · doi:10.1371/journal.pone.0026962 · Cited by 56 · see citing works
Selective BET bromodomain inhibition as an antifungal therapeutic strategy
Mietton, F., Ferri, E., Champleboux, M., Zala, N., Maubon, D., Zhou, Y., Harbut, M., Spittler, D., Garnaud, C., Courçon, M., et al. (2017) · Nature Communications · doi:10.1038/ncomms15482 · Cited by 53 · see citing works
Suliman, H. S., Appling, D. R., & Robertus, J. D. (2007) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2007.09.003 · Cited by 50 · see citing works
Burrack, L. S., Applen, S. E., & Berman, J. G. (2011) · Current Biology · doi:10.1016/j.cub.2011.04.002 · Cited by 50 · see citing works
Self-citationMolecular Biology of Maize Ac/Ds Elements: An Overview
Lazarow, K., Doll, M.-L., & Kunze, R. (2013) · Methods in molecular biology · doi:10.1007/978-1-62703-568-2_5 · Cited by 49 · see citing works
Self-citationVanderSluis, B., Costanzo, M., Billmann, M., Ward, H. N., Myers, C. L., Andrews, B., & Boone, C. M. (2018) · Current Opinion in Microbiology · doi:10.1016/j.mib.2018.06.004 · Cited by 49 · see citing works
Genetic Network Complexity Shapes Background-Dependent Phenotypic Expression
Hou, J., van Leeuwen, J. S., Andrews, B., & Boone, C. M. (2018) · Trends in Genetics · doi:10.1016/j.tig.2018.05.006 · Cited by 41 · see citing works
Carr, P. D., Tuckwell, D. S., Hey, P., Simon, L., d’Enfert, C., Birch, M., Oliver, J. D., & Bromley, M. (2010) · Eukaryotic Cell · doi:10.1128/ec.00324-09 · Cited by 37 · see citing works
Genetic backgrounds and hidden trait complexity in natural populations
Fournier, T., & Schacherer, J. (2017) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2017.08.009 · Cited by 36 · see citing works
A Hyperactive Transposase of the Maize Transposable ElementActivator(Ac)
Lazarow, K., Du, M.-L., Weimer, R., & Kunze, R. (2012) · Genetics · doi:10.1534/genetics.112.139642 · Cited by 34 · see citing works
Self-citationChemogenomic Profiling of the Fungal Pathogen Candida albicans
Chen, Y., Mallick, J., Maqnas, A., Sun, Y., Choudhury, B. I., Côte, P., Yan, L., Ni, T., Li, Y., Zhang, D., et al. (2017) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02365-17 · Cited by 30 · see citing works
Maize Transposable Elements Ac/Ds as Insertion Mutagenesis Tools in Candida albicans
Mielich, K., Shtifman‐Segal, E., Golz, J. C., Zeng, G., Wang, Y., Berman, J. G., & Kunze, R. (2018) · G3 Genes Genomes Genetics · doi:10.1534/g3.117.300388 · Cited by 29 · see citing works
Self-citationEvolution of small nuclear RNAs in S. cerevisiae, C. albicans, and other hemiascomycetous yeasts
Mitrovich, Q. M., & Guthrie, C. (2007) · RNA · doi:10.1261/rna.766607 · Cited by 28 · see citing works
One-step targeted gene deletion in Candida albicans haploids
Zeng, G., Wang, Y., Chan, F. Y., & Wang, Y. (2014) · Nature Protocols · doi:10.1038/nprot.2014.029 · Cited by 24 · see citing works
Using the Candida Genome Database
Skrzypek, M. S., Binkley, J., & Sherlock, G. J. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-7737-6_3 · Cited by 18 · see citing works
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Drug resistance and tolerance in fungi.
Berman, J., & Krysan, D. J. (2020) · Nature Reviews Microbiology · doi:10.1038/s41579-019-0322-2 · Cited by 654 · see citing works
Self-citationThe importance of antimicrobial resistance in medical mycology
Gow, N. A. R., Johnson, C., Berman, J. G., Coste, A. T., Cuomo, C. A., Perlin, D. S., Bicanic, T. A., Harrison, T. S., Wiederhold, N. P., Bromley, M., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-32249-5 · Cited by 228 · see citing works
Self-citationCandida albicans and Candida glabrata : global priority pathogens
Katsipoulaki, M., Stappers, M. H. T., Malavia, D., Brunke, S., Hube, B., & Gow, N. A. R. (2024) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00021-23 · Cited by 174 · see citing works
Self-citationExtensive loss of cell-cycle and DNA repair genes in an ancient lineage of bipolar budding yeasts
Steenwyk, J. L., Opulente, D. A., Kominek, J., Shen, X.-X., Zhou, X., Labella, A. L., Bradley, N. P., Eichman, B. F., Čadež, N., Libkind, D., et al. (2019) · PLoS Biology · doi:10.1371/journal.pbio.3000255 · Cited by 162 · see citing works
Self-citationFrom Jekyll to Hyde: The Yeast–Hyphal Transition of Candida albicans
Chow, E. W. L., Pang, L. M., & Wang, Y. (2021) · Pathogens · doi:10.3390/pathogens10070859 · Cited by 144 · see citing works
Current trends, limitations and future research in the fungi?
Hyde, K. D., Baldrian, P., Chen, Y., Chethana, K. W. T., de Hoog, S., Doilom, M., de Farias, A. R. G., Gonçalves, M. F. M., Gonkhom, D., Gui, H., et al. (2024) · Fungal diversity · doi:10.1007/s13225-023-00532-5 · Cited by 107 · see citing works
Cellular quiescence in budding yeast
Sun, S., & Gresham, D. (2020) · Yeast · doi:10.1002/yea.3545 · Cited by 102 · see citing works
Lu, H., Hong, T., Jiang, Y., Whiteway, M. S., & Zhang, S. (2023) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2023.114960 · Cited by 96 · see citing works
Fu, C., Zhang, X., Veri, A. O., Iyer, K. R., Lash, E., Xue, A., Yan, H., Revie, N. M., Wong, C. J., Lin, Z., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-26850-3 · Cited by 82 · see citing works
Orozco-Arias, S., Piña, J. S., Tabares-Soto, R., Castillo, L., Guyot, R., & Isaza, G. A. (2020) · Processes · doi:10.3390/pr8060638 · Cited by 76 · see citing works
A CRISPR Interference Platform for Efficient Genetic Repression in Candida albicans
Wensing, L. F., Sharma, J., Uthayakumar, D., Proteau, Y., Chavez, A., & Shapiro, R. S. (2019) · mSphere · doi:10.1128/msphere.00002-19 · Cited by 70 · see citing works
The CRISPR toolbox in medical mycology: State of the art and perspectives
Morio, F., Lombardi, L., & Butler, G. (2020) · PLoS Pathogens · doi:10.1371/journal.ppat.1008201 · Cited by 65 · see citing works
Plasmid-Based CRISPR-Cas9 Gene Editing in Multiple Candida Species
Lombardi, L., Oliveira-Pacheco, J., & Butler, G. (2019) · mSphere · doi:10.1128/msphere.00125-19 · Cited by 63 · see citing works
Overcoming Fungal Echinocandin Resistance through Inhibition of the Non-essential Stress Kinase Yck2
Caplan, T., Lorente-Macías, Á., Stogios, P. J., Evdokimova, E., Hyde, S., Wellington, M. A., Liston, S., Iyer, K. R., Puumala, E., Shekhar-Guturja, T., et al. (2020) · Cell Chemical Biology · doi:10.1016/j.chembiol.2019.12.008 · Cited by 57 · see citing works
Transposon Insertion Sequencing, a Global Measure of Gene Function
van Opijnen, T., & Levin, H. L. (2020) · Annual Review of Genetics · doi:10.1146/annurev-genet-112618-043838 · Cited by 57 · see citing works
Gale, A. N., Sakhawala, R. M., Levitan, A., Sharan, R., Berman, J., Timp, W., & Cunningham, K. W. (2020) · G3 Genes|Genomes|Genetics · doi:10.1534/g3.120.401595 · Cited by 56 · see citing works
Self-citationMohammad, H. T., Eldesouky, H. E., Hazbun, T. R., Mayhoub, A. S., & Seleem, M. N. (2019) · Scientific Reports · doi:10.1038/s41598-019-55379-1 · Cited by 54 · see citing works
Gusa, A. A., Yadav, V., Roth, C., Williams, J. D., Shouse, E. M., Magwene, P. M., Heitman, J., & Jinks-Robertson, S. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2209831120 · Cited by 55 · see citing works
Systematic analysis of bypass suppression of essential genes
van Leeuwen, J. S., Pons, C., Tan, G., Wang, J. Z., Hou, J., Weile, J., Gebbia, M., Liang, W., Shuteriqi, E., Li, Z., et al. (2020) · Molecular Systems Biology · doi:10.15252/msb.20209828 · Cited by 52 · see citing works
Recent advances in understanding Candida albicans hyphal growth
Arkowitz, R. A., & Bassilana, M. (2019) · F1000Research · doi:10.12688/f1000research.18546.1 · Cited by 51 · see citing works
Candida albicans Pma1p Contributes to Growth, pH Homeostasis, and Hyphal Formation
Rane, H. S., Hayek, S. R., Frye, J. E., Abeyta, E. L., Bernardo, S. M., Parra, K. J., & Lee, S. A. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.01012 · Cited by 50 · see citing works
CRISPR-Based Genetic Manipulation of Candida Species: Historical Perspectives and Current Approaches
Uthayakumar, D., Sharma, J., Wensing, L. F., & Shapiro, R. S. (2021) · Frontiers in Genome Editing · doi:10.3389/fgeed.2020.606281 · Cited by 48 · see citing works
Calcium-calcineurin signaling pathway in Candida albicans: A potential drug target
Li, W., Shrivastava, M., Lu, H., & Jiang, Y. (2021) · Microbiological Research · doi:10.1016/j.micres.2021.126786 · Cited by 47 · see citing works
DeJarnette, C. A., Luna-Tapia, A., Estredge, L. R., & Palmer, G. E. (2020) · mSphere · doi:10.1128/msphere.00374-20 · Cited by 48 · see citing works
Candida albicans: An Emerging Yeast Model to Study Eukaryotic Genome Plasticity
Legrand, M., Jaitly, P., Feri, A., d’Enfert, C., & Sanyal, K. (2019) · Trends in Genetics · doi:10.1016/j.tig.2019.01.005 · Cited by 45 · see citing works
Orozco-Arias, S., Isaza, G. A., Guyot, R., & Tabares-Soto, R. (2019) · PeerJ · doi:10.7717/peerj.8311 · Cited by 43 · see citing works
Metabolic Reprogramming in the Opportunistic Yeast Candida albicans in Response to Hypoxia
Burgain, A., Tebbji, F., Khemiri, I., & Sellam, A. (2020) · mSphere · doi:10.1128/msphere.00913-19 · Cited by 41 · see citing works
The Candida Genome Database: annotation and visualization updates
Lew-Smith, J., Binkley, J., & Sherlock, G. J. (2025) · Genetics · doi:10.1093/genetics/iyaf001 · Cited by 37 · see citing works
Fungal resilience and host–pathogen interactions: Future perspectives and opportunities
Brown, A. J. P. (2022) · Parasite Immunology · doi:10.1111/pim.12946 · Cited by 40 · see citing works
Lee, S. Y., Hung, S., Esnault, C., Pathak, R., Johnson, K. R., Bankole, O., Yamashita, A., Zhang, H., & Levin, H. L. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.01.094 · Cited by 32 · see citing works
Fu, C., Beattie, S. R., Jezewski, A. J., Robbins, N., Whitesell, L., Krysan, D. J., & Cowen, L. E. (2022) · Genetics · doi:10.1093/genetics/iyab164 · Cited by 31 · see citing works
Structure-guided approaches to targeting stress responses in human fungal pathogens
LeBlanc, E. V., Polvi, E. J., Veri, A. O., Privé, G. G., & Cowen, L. E. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.rev120.013731 · Cited by 31 · see citing works
Scott, J., Sueiro-Olivares, M., Thornton, B. P., Owens, R. A., Muhamadali, H., Fortune‐Grant, R., Thomson, D. D., Thomas, R., Hollywood, K. A., Doyle, S., et al. (2020) · mBio · doi:10.1128/mbio.01985-20 · Cited by 30 · see citing works
Novel Promising Antifungal Target Proteins for Conquering Invasive Fungal Infections
Zhen, C., Lu, H., & Jiang, Y. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.911322 · Cited by 33 · see citing works
Lu, H., Li, W., Whiteway, M., Wang, H., Zhu, S., Ji, Z., Feng, Y., Yan, L., Fang, T., Li, L., et al. (2023) · mBio · doi:10.1128/mbio.02639-22 · Cited by 30 · see citing works
Sanchez, M. R., Payen, C., Cheong, F., Hovde, B. T., Bissonnette, S. A., Arkin, A. P., Skerker, J. M., Brem, R. B., Caudy, A. A., & Dunham, M. J. (2019) · Genome Research · doi:10.1101/gr.232330.117 · Cited by 28 · see citing works
Heredia, M. Y., Ikeh, M. A. C., Gunasekaran, D., Conrad, K. A., Filimonava, S., Marotta, D. H., Nobile, C. J., & Rauceo, J. M. (2020) · PLoS Genetics · doi:10.1371/journal.pgen.1008908 · Cited by 29 · see citing works
Gutierrez-Perez, C., & Cramer, R. A. (2025) · npj Antimicrobials and Resistance · doi:10.1038/s44259-025-00093-4 · Cited by 33 · see citing works
Steenwyk, J. L., Phillips, M. A., Yang, F. J., Date, S. S., Graham, T. R., Berman, J. G., Hittinger, C. T., & Rokas, A. (2022) · Science Advances · doi:10.1126/sciadv.abn0105 · Cited by 23 · see citing works
Self-citationSnyder, N. A., Kim, A., Kester, L., Gale, A. N., Studer, C., Hoepfner, D., Roggo, S. P., Helliwell, S. B., & Cunningham, K. W. (2019) · G3 Genes Genomes Genetics · doi:10.1534/g3.118.200748 · Cited by 21 · see citing works
Levitan, A., Gale, A. N., Dallon, E., Kozan, D. W., Cunningham, K. W., Sharan, R., & Berman, J. G. (2020) · Current Genetics · doi:10.1007/s00294-020-01096-6 · Cited by 25 · see citing works
Self-citationModulation of the complex regulatory network for methionine biosynthesis in fungi
Shrivastava, M., Feng, J., Coles, M., Clark, B., Islam, A., Dumeaux, V., & Whiteway, M. S. (2021) · Genetics · doi:10.1093/genetics/iyaa049 · Cited by 24 · see citing works
Ennis, C. L., Hernday, A. D., & Nobile, C. J. (2021) · Microbiology Spectrum · doi:10.1128/spectrum.01820-21 · Cited by 22 · see citing works
Genetic Modification of Closely Related Candida Species
Mancera, E., Frazer, C., Porman, A. M., Ruiz‐Castro, S., Johnson, A. D., & Bennett, R. J. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.00357 · Cited by 22 · see citing works
DeORFanizing Candida albicans Genes using Coexpression
O’Meara, T. R., & O’Meara, M. J. (2021) · mSphere · doi:10.1128/msphere.01245-20 · Cited by 20 · see citing works
Chen, P., Michel, A. H., & Zhang, J. (2022) · Nature Communications · doi:10.1038/s41467-022-29228-1 · Cited by 19 · see citing works
Hgc1 Independence of Biofilm Hyphae in Candida albicans
Sharma, A., Solis, N. V., Huang, M. Y., Lanni, F., Filler, S. G., & Mitchell, A. P. (2023) · mBio · doi:10.1128/mbio.03498-22 · Cited by 18 · see citing works
Li, Z., Wang, H., Cai, C., Wong, A. H., Wang, J., Gao, J., & Wang, Y. (2020) · Nature Protocols · doi:10.1038/s41596-020-0351-3 · Cited by 18 · see citing works
Respiration supports intraphagosomal filamentation and escape of Candida albicans from macrophages
Case, N. T., Westman, J., Hallett, M. T., Plumb, J. D., Farheen, A., Maxson, M. E., MacAlpine, J., Liston, S. D., Hube, B., Robbins, N., et al. (2023) · mBio · doi:10.1128/mbio.02745-23 · Cited by 17 · see citing works
Mobile genetic element-based gene editing and genome engineering: Recent advances and applications
Hwang, J., Ye, D.-Y., Jung, G. Y., & Jang, S. (2024) · Biotechnology Advances · doi:10.1016/j.biotechadv.2024.108343 · Cited by 18 · see citing works
Wu, H., Ji, Z., Huang, X., Li, L.-P., Hang, S.-J., Yu, J., Lu, H., & Jiang, Y.-Y. (2024) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.4c00399 · Cited by 16 · see citing works
Billmyre, R. B., Craig, C. J., Lyon, J. W., Reichardt, C., Kuhn, A. M., Eickbush, M. T., & Zanders, S. E. (2025) · PLoS Biology · doi:10.1371/journal.pbio.3003184 · Cited by 17 · see citing works
Exploring conditional gene essentiality through systems genetics approaches in yeast
Bosch-Guiteras, N., & van Leeuwen, J. S. (2022) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2022.101963 · Cited by 17 · see citing works
Regulation of heme utilization and homeostasis in Candida albicans
Andrawes, N., Weissman, Z., Pinsky, M., Moshe, S., Berman, J., & Kornitzer, D. (2022) · PLOS Genetics · doi:10.1371/journal.pgen.1010390 · Cited by 17 · see citing works
Self-citationAdvances in Molecular Tools and In Vivo Models for the Study of Human Fungal Pathogenesis
Malavia, D., Gow, N. A. R., & Usher, J. (2020) · Microorganisms · doi:10.3390/microorganisms8060803 · Cited by 15 · see citing works
Self-citationRashid, S., Correia-Mesquita, T. O., Godoy, P., Omran, R. P., & Whiteway, M. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.764711 · Cited by 15 · see citing works
Billmyre, R. B., Eickbush, M. T., Craig, C. J., Lange, J. J., Wood, C. J., Helston, R. M., & Zanders, S. E. (2022) · PLoS Genetics · doi:10.1371/journal.pgen.1010462 · Cited by 15 · see citing works
Selection or drift: The population biology underlying transposon insertion sequencing experiments
Mahmutovic, A., Wiesch, P. A. Z., & Abel, S. (2020) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2020.03.021 · Cited by 14 · see citing works
Michel, A. H., van Schie, S. N. S., Mosbach, A., Scalliet, G., & Kornmann, B. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/866483 · Cited by 13 · see citing works
SAturated Transposon Analysis in Yeast (SATAY) for Deep Functional Mapping of Yeast Genomes
Michel, A. H., & Kornmann, B. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-2257-5_20 · Cited by 14 · see citing works
The phosphatome of opportunistic pathogen Candida species
Szabó, K., Miskei, M., Farkas, I., & Dombrádi, V. (2021) · Fungal Biology Reviews · doi:10.1016/j.fbr.2020.12.002 · Cited by 13 · see citing works
A Myosin Light Chain Is Critical for Fungal Growth Robustness in Candida albicans
Puerner, C. T. S., Serrano, A., Wakade, R. S., Bassilana, M., & Arkowitz, R. A. (2021) · mBio · doi:10.1128/mbio.02528-21 · Cited by 12 · see citing works
Wensing, L. F., & Shapiro, R. S. (2021) · Methods in molecular biology · doi:10.1007/978-1-0716-1720-5_4 · Cited by 13 · see citing works
Copy number variation alters local and global mutational tolerancePreprint
Avecilla, G., Spealman, P., Matthews, J. C., Caudal, É., Schacherer, J., & Gresham, D. (2023) · Genome Research · doi:10.1101/gr.277625.122 · Cited by 13 · see citing works
Xiong, E. H., Zhang, X., Yan, H., Ward, H. N., Lin, Z., Wong, C. J., Fu, C., Gingras, A., Noble, S. M., Robbins, N., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114601 · Cited by 12 · see citing works
Exploring the druggable proteome of Candida species through comprehensive computational analysis
Mukherjee, S., Kundu, I., Askari, M., Barai, R. S., Venkatesh, K. V., & Idicula‐Thomas, S. (2021) · Genomics · doi:10.1016/j.ygeno.2020.12.040 · Cited by 12 · see citing works
Genomic Approaches to Antifungal Drug Target Identification and Validation
Robbins, N., & Cowen, L. E. (2022) · Annual Review of Microbiology · doi:10.1146/annurev-micro-041020-094524 · Cited by 13 · see citing works
Dantuluri, S., Schwer, B., Abdullahu, L., Damha, M. J., & Shuman, S. (2021) · RNA · doi:10.1261/rna.078660.120 · Cited by 12 · see citing works
Evolution and strain diversity advance exploration of Candida albicans biology
Anderson, M. Z., & Dietz, S. M. (2024) · mSphere · doi:10.1128/msphere.00641-23 · Cited by 11 · see citing works
The SAGA and NuA4 component Tra1 regulates Candida albicans drug resistance and pathogenesis
Razzaq, I., Berg, M. D., Jiang, Y., Genereaux, J. L., Uthayakumar, D., Kim, G. H., Agyare-Tabbi, M. R., Halder, V., Brandl, C. J., Lajoie, P., et al. (2021) · Genetics · doi:10.1093/genetics/iyab131 · Cited by 9 · see citing works
Nickels, T. J., Gale, A. N., Harrington, A. A., Timp, W., & Cunningham, K. W. (2024) · G3 Genes Genomes Genetics · doi:10.1093/g3journal/jkae173 · Cited by 10 · see citing works
The identification of essential cellular genes is critical for validating drug targets
Xu, T., Wang, S., Ma, T., Dong, Y., Ashby, C. R., & Hao, G. (2024) · Drug Discovery Today · doi:10.1016/j.drudis.2024.104215 · Cited by 9 · see citing works
The renaissance of yeasts as microbial factories in the modern age of biomanufacturing
Payen, C., & Thompson, D. A. (2019) · Yeast · doi:10.1002/yea.3439 · Cited by 9 · see citing works
A data library of Candida albicans functional genomic screens
Gervais, N. C., Halder, V., & Shapiro, R. S. (2021) · FEMS Yeast Research · doi:10.1093/femsyr/foab060 · Cited by 8 · see citing works
Rizzo, M., Soisangwan, N., Vega, S. B. P., Price, R. J., Uyl, C., Iracane, E., Shaw, M., Soetaert, J., Selmecki, A. M., & Buscaino, A. (2022) · PLoS Genetics · doi:10.1371/journal.pgen.1010576 · Cited by 8 · see citing works
Ruiz-Castilla, F. J., Bieber, J., Caro, G., Michán, C., Sychrová, H., & Ramos, J. (2020) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2020.183486 · Cited by 9 · see citing works
Banerjee, A., Goldgur, Y., Schwer, B., & Shuman, S. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz1049 · Cited by 8 · see citing works
Isolation and characterization of haploid heterothallic beer yeasts
Badura, J., Bernardi, B., Muno-Bender, J., Matti, K., Zimmer, K., & Wendland, J. (2025) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-024-13397-8 · Cited by 7 · see citing works
Application of the Mutant Libraries for Candida albicans Functional Genomics
Wang, R., Liu, J., Liu, Y., Lv, Q., & Yan, L. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232012307 · Cited by 8 · see citing works
Structural basis for Tpt1-catalyzed 2′-PO 4 transfer from RNA and NADP(H) to NAD +
Jacewicz, A., Dantuluri, S., & Shuman, S. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2312999120 · Cited by 7 · see citing works
Molaeitabari, A., & Dahms, T. E. S. (2025) · Microbiology Spectrum · doi:10.1128/spectrum.02754-24 · Cited by 7 · see citing works
Marton, T., Feri, A., Commère, P., Maufrais, C., d’Enfert, C., & Legrand, M. (2019) · mSphere · doi:10.1128/msphere.00709-18 · Cited by 6 · see citing works
Shoukat, I., Frazer, C., & Allingham, J. S. (2019) · mSphere · doi:10.1128/msphere.00610-19 · Cited by 7 · see citing works
Dantuluri, S., Abdullahu, L., Munir, A., Katolik, A., Damha, M. J., & Shuman, S. (2020) · RNA · doi:10.1261/rna.074377.119 · Cited by 7 · see citing works
Cellular Localization of Carbonic Anhydrase Nce103p in Candida albicans and Candida parapsilosis
Dostál, J., Bláha, J., Hadravová, R., Hubálek, M., Hrušková‐Heidingsfeldová, O., & Pichová, I. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21030850 · Cited by 7 · see citing works
Candida albicans Potassium Transporters
Ruiz-Castilla, F. J., Ruiz-Pérez, F., Ramos‐Moreno, L., & Ramos, J. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23094884 · Cited by 7 · see citing works
Kuplińska, A., Rząd, K., Wojciechowski, M., Milewski, S., & Gabriel, I. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23147763 · Cited by 7 · see citing works
Hijacking Transposable Elements for Saturation Mutagenesis in Fungi
Schrevens, S., & Sanglard, D. (2021) · Frontiers in Fungal Biology · doi:10.3389/ffunb.2021.633876 · Cited by 7 · see citing works
Billmyre, R. B., Craig, C. J., Lyon, J. W., Reichardt, C., Eickbush, M. T., & Zanders, S. E. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.07.28.605507 · Cited by 7 · see citing works
Discovery and mechanism of a highly selective, antifungal acetyl-CoA synthetase inhibitor
Jezewski, A. J., Alden, K. M., Propp, J., Daraji, D. G., Lail, C. L., Heene, M. E., Fuller, A. J., Ferreira, J. C., Liu, L., Battaile, K. P., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-64183-7 · Cited by 6 · see citing works
New approaches to tackle a rising problem: Large-scale methods to study antifungal resistance
Després, P. C., Shapiro, R. S., & Cuomo, C. A. (2024) · PLoS Pathogens · doi:10.1371/journal.ppat.1012478 · Cited by 6 · see citing works
Huang, M. Y., Nalley, M. J., Hecht, P. C., & Madhani, H. D. (2025) · G3 Genes Genomes Genetics · doi:10.1093/g3journal/jkaf071 · Cited by 6 · see citing works
Jung, K., Kwon, S., Jung, J., & Bahn, Y. (2022) · Microbiology Spectrum · doi:10.1128/spectrum.01044-22 · Cited by 6 · see citing works
Swenson, K. A., Alberti, L., Teele, K., Yadav, A., Shah, S. J., & Konopka, J. B. (2025) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00229-24 · Cited by 6 · see citing works
Bian, Z., Xu, Z. Z., Peer, A., Choi, Y., Priest, S. J., Akritidou, K., Dasgupta, A., Dahlmann, T. A., Kück, U., Nowrousian, M., et al. (2025) · mBio · doi:10.1128/mbio.00223-25 · Cited by 5 · see citing works
From patterns to prediction: machine learning and antifungal resistance biomarker discovery
Thorn, V., & Xu, J. (2025) · Canadian Journal of Microbiology · doi:10.1139/cjm-2024-0248 · Cited by 5 · see citing works
PRACTICAL APPLICATIONS OF MACHINE LEARNING FOR ANTI-INFECTIVE DRUG DISCOVERY
Sarkar, N., & Stokes, J. M. (2023) · Medicinal chemistry reviews · doi:10.1021/mc-2023-vol58.ch14 · Cited by 5 · see citing works
Pseudouridine synthase 7 impacts Candida albicans rRNA processing and morphological plasticity
Pickerill, E. S., Kurtz, R. P., Tharp, A., Sanz, P. G., Begum, M., & Bernstein, D. A. (2019) · Yeast · doi:10.1002/yea.3436 · Cited by 5 · see citing works
Jaitly, P., Legrand, M., Das, A., Patel, T., Chauvel, M., Maufrais, C., d’Enfert, C., & Sanyal, K. (2022) · Nature Communications · doi:10.1038/s41467-022-31980-3 · Cited by 6 · see citing works
Pooled CRISPRi screening reveals fungal-specific drug target candidates
Wensing, L. F., Després, P. C., Francis, D., Fogal, M., Hendriks, A., Gervais, N. C., Fikry, C., Bukari, A.-R. A., Gerstein, A. C., Cuomo, C. A., et al. (2026) · Nature Microbiology · doi:10.1038/s41564-026-02356-w · Cited by 4 · see citing works
- Authors
- Segal, E. S., Gritsenko, V., Levitan, A., Yadav, B., Dror, N., Steenwyk, J. L., Silberberg, Y., Mielich, K., Rokas, A., Gow, N. A. R., Kunze, R., Sharan, R., & Berman, J.
- Affiliations
- Tel Aviv University (IL)
- University of Aberdeen (GB)
- Vanderbilt University (US)
- Freie Universität Berlin (DE)
- Corresponding author
- Berman, Judith
- ORCID
- Venue
- mBio
- Publisher
- American Society for Microbiology
- Published
- 2018-11-07
- Volume
- 9
- Issue
- 5
- ISSN
- 2150-7511 (ISSN-L)
- 2161-2129
- PMC
- PMC6212825
- OpenAlex
- W2898801056
- Cited by
- 150
- References
- 105
- Citations by year
- 2026: 11 · 2025: 20 · 2024: 18 · 2023: 9 · 2022: 21 · 2021: 20 · 2020: 26 · 2019: 24 · 2018: 1
- FWCI
- 6.31
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- mBio (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Aberdeen University Research Archive (Aberdeen University) (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Refubium (Universitätsbibliothek der Freien Universität Berlin) (submittedVersion, cc-by)
- Universitätsbibliothek der FU Berlin Hochschulschriftenstelle u. Dokumentenserver (cc-by)
- Funders
- Wellcome Trust (086827 075470 101873 200208)
- MRC Center for Medical Mycology (N006364/1)
- European Research Council (340087 RAPLODAPT)
- Dahlem Center of Plant Sciences (DCPS)
- Israel Science Foundation (715/18)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
- Keywords
- gene essentiality, Candida albicans, transposon mutagenesis, essential genes, fungal pathogens, antifungal drug targets, machine learning, deep sequencing
- MeSH terms
- Machine Learning, Aspergillus fumigatus, Candida albicans, Cryptococcus neoformans, DNA Transposable Elements, Genes, Fungal, Genetics, Microbial, Haploidy, Histoplasma, Mutagenesis, Insertional, Genes, Essential
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