SUT1-promoted sterol uptake involves the ABC transporter Aus1 and the mannoprotein Dan1 whose synergistic action is sufficient for this process
Open accessAbstract
Efficient sterol influx in the yeast Saccharomyces cerevisiae is restricted to anaerobiosis or to haem deficiency resulting from mutations. Constitutive expression of SUT1, an hypoxic gene encoding a transcriptional regulator, induces sterol uptake in aerobiosis. A genome-wide approach using DNA microarray was used to identify the mediators of SUT1 effects on aerobic sterol uptake. A total of 121 ORFs (open reading frames) were significantly and differentially expressed after SUT1 overexpression, 61 down-regulated and 60 up-regulated. Among these genes, the role of the putative ABC transporter (ATP-binding-cassette transporter) Aus1, and of the cell-wall mannoprotein Dan1, was characterized better. These two genes play an essential role in aerobic sterol uptake, since their deletion compromised the SUT1 effects, but individual overexpression of either of these genes in a wild-type background was not sufficient for this process. However, constitutive co-expression of AUS1 and DAN1 in a wild-type background resulted in sterol influx in aerobiosis. These results suggest that the corresponding proteins may act synergistically in vivo to promote sterol uptake.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
The overexpression of DAN1 and AUS1 is sufficient to promote the uptake of sterol in aerobiosis.
“In fact, the overexpression of DAN1 and AUS1 is sufficient to promote the uptake of sterol in aerobiosis [105].”
From Regulation of Ergosterol Biosynthesis in Saccharomyces cerevisiae (2020) · cites this paper as [105]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Yang, Y., Dudoit, S., Luu, P., Lin, D., Peng, V., Ngai, J., & Speed, T. (2002) · Nucleic Acids Research · doi:10.1093/nar/30.4.e15 · Cited by 3,722 · see citing works
Transformation in yeast: Development of a hybrid cloning vector and isolation of the can1 gene
Broach, J. R., Strathern, J. N., & Hicks, J. B. (1979) · Gene · doi:10.1016/0378-1119(79)90012-x · Cited by 1,073 · see citing works
Construction of a set of convenient saccharomyces cerevisiae strains that are isogenic to S288C
Winston, F., Dollard, C. A., & Ricupero‐Hovasse, S. L. (1995) · Yeast · doi:10.1002/yea.320110107 · Cited by 949 · see citing works
Ssn6-Tup1 is a general repressor of transcription in yeast
Keleher, C. A., Redd, M. J., Schultz, J., Carlson, M., & Johnson, A. D. (1992) · Cell · doi:10.1016/0092-8674(92)90146-4 · Cited by 666 · see citing works
Sauer, N., & Stolz, J. (1994) · The Plant Journal · doi:10.1046/j.1365-313x.1994.6010067.x · Cited by 375 · see citing works
Proft, M., & Struhl, K. (2002) · Molecular Cell · doi:10.1016/s1097-2765(02)00557-9 · Cited by 350 · see citing works
Upc2p and Ecm22p, Dual Regulators of Sterol Biosynthesis in <i>Saccharomyces cerevisiae</i>
Vik, Å., & Rine, J. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.19.6395-6405.2001 · Cited by 277 · see citing works
Linde, J. J. M. T., Liang, H., Davis, R. W., Steensma, H. Y., van Dijken, J. P., & Pronk, J. T. (1999) · Journal of Bacteriology · doi:10.1128/jb.181.24.7409-7413.1999 · Cited by 268 · see citing works
Shitan, N., Bazin, I., Dan, K., Obata, K., Kigawa, K., Ueda, K., Sato, F., Forestier, C., & Yazaki, K. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0134257100 · Cited by 267 · see citing works
Wilcox, L. J., Balderes, D. A., Wharton, B., Tinkelenberg, A. H., Rao, G., & Sturley, S. L. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m204707200 · Cited by 250 · see citing works
Kwast, K. E., Lai, L., Menda, N. S., James, D. T., Aref, S., & Burke, P. V. (2002) · Journal of Bacteriology · doi:10.1128/jb.184.1.250-265.2002 · Cited by 232 · see citing works
Microarray Expression Profiling Identifies Genes with Altered Expression in HDL-Deficient MicePreprint
Callow, M. J. (2000) · Genome Research · doi:10.1101/gr.10.12.2022 · Cited by 228 · see citing works
Agarwal, A. K., Rogers, P. D., Baerson, S. R., Jacob, M. R., Barker, K. S., Cleary, J. D., Walker, L. A., Nagle, D. G., & Clark, A. M. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m306291200 · Cited by 204 · see citing works
Balasubramanian, B., Lowry, C. V., & Zitomer, R. S. (1993) · Molecular and Cellular Biology · doi:10.1128/mcb.13.10.6071 · Cited by 140 · see citing works
ABC transporters in cellular lipid trafficking
Schmitz, G., Kaminski, W. E., & Orsó, E. (2000) · Current Opinion in Lipidology · doi:10.1097/00041433-200010000-00007 · Cited by 136 · see citing works
A microarray‐assisted screen for potential Hap1 and Rox1 target genes in Saccharomyces cerevisiae
Linde, J. J. M. T., & Steensma, H. Y. (2002) · Yeast · doi:10.1002/yea.879 · Cited by 123 · see citing works
Smriti, S., Krishnamurthy, S., Dixit, B. L., Gupta, C. M., Milewski, S., & Prasad, R. (2002) · Yeast · doi:10.1002/yea.818 · Cited by 113 · see citing works
Deckert, J., Perini, R. F., Balasubramanian, B., & Zitomer, R. S. (1995) · Genetics · doi:10.1093/genetics/139.3.1149 · Cited by 101 · see citing works
Synergistic repression of anaerobic genes by Mot3 and Rox1 in Saccharomyces cerevisiae
Sertil, O. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkg792 · Cited by 88 · see citing works
Conlan, R. S., Gounalaki, N., Hatzis, P., & Tzamarias, D. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.1.205 · Cited by 87 · see citing works
Pleiotropic mutations in Saccharomyces cerevisiae affecting sterol uptake and metabolism
Lewis, T. L., Keesler, G. A., Fenner, G. P., & Parks, L. W. (1988) · Yeast · doi:10.1002/yea.320040203 · Cited by 80 · see citing works
Isolation and characterization of the Saccharomyces cerevisiae SUT1 gene involved in sterol uptake
Bourot, S., & Karst, F. (1995) · Gene · doi:10.1016/0378-1119(95)00478-o · Cited by 76 · see citing works
Involvement of heme biosynthesis in control of sterol uptake by Saccharomyces cerevisiae
Lewis, T. A., Taylor, F. R., & Parks, L. W. (1985) · Journal of Bacteriology · doi:10.1128/jb.163.1.199-207.1985 · Cited by 67 · see citing works
Ness, F., Bourot, S., Régnacq, M., Spagnoli, R., Bergès, T., & Karst, F. (2001) · European Journal of Biochemistry · doi:10.1046/j.1432-1327.2001.02029.x · Cited by 66 · see citing works
Shianna, K. V., Dotson, W. D., Tove, S. R., & Parks, L. W. (2001) · Journal of Bacteriology · doi:10.1128/jb.183.3.830-834.2001 · Cited by 63 · see citing works
Cordier, H. L., Karst, F., & Bergès, T. (1999) · Plant Molecular Biology · doi:10.1023/a:1006181720100 · Cited by 52 · see citing works
Balasubramanian, B., Lowry, C. V., & Zitomer, R. S. (1993) · Molecular and Cellular Biology · doi:10.1128/mcb.13.10.6071-6078.1993 · Cited by 48 · see citing works
Evidence that TUP1/SSN6 has a positive effect on the activity of the yeast activator HAP1.
Zhang, L., & Guarente, L. (1994) · Genetics · doi:10.1093/genetics/136.3.813 · Cited by 44 · see citing works
Microarray Expression Profiling Identifies Genes with Altered Expression in HDL-Deficient MicePreprint
Callow, M. J., Dudoit, S., Gong, E. L., et al. (2000) · Genome Research · doi:10.1101/gr.147200 · Cited by 43 · see citing works
Ness, F., Achstetter, T., Duport, C., Karst, F., Spagnoli, R., & Degryse, E. (1998) · Journal of Bacteriology · doi:10.1128/jb.180.7.1913-1919.1998 · Cited by 42 · see citing works
Régnacq, M., Alimardani, P., Moudni, B. E., & Bergès, T. (2001) · Molecular Microbiology · doi:10.1046/j.1365-2958.2001.02450.x · Cited by 39 · see citing works
SUT1suppressessec14–1through upregulation ofCSR1inSaccharomyces cerevisiae
Régnacq, M., Ferreira, T., Puard, J., & Bergès, T. (2002) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2002.tb11431.x · Cited by 13 · see citing works
Zhang, J. (2001) · Molecular Membrane Biology · doi:10.1080/09687680110048831 · Cited by 11 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Cell wall construction in Saccharomyces cerevisiae
Klis, F. M., Boorsma, A., & de Groot, P. W. J. (2006) · Yeast · doi:10.1002/yea.1349 · Cited by 776 · see citing works
Regulation of Ergosterol Biosynthesis in Saccharomyces cerevisiae
Jordá, T., & Puig, S. (2020) · Genes · doi:10.3390/genes11070795 · Cited by 489 · see citing works
FLO1 Is a Variable Green Beard Gene that Drives Biofilm-like Cooperation in Budding Yeast
Smukalla, S. M., Caldara, M., Pochet, N. L. M. M., Beauvais, A., Guadagnini, S., Chen, Y., Vinces, M. D., Jansen, A., Prévost, M. C., Latgé, J., et al. (2008) · Cell · doi:10.1016/j.cell.2008.09.037 · Cited by 453 · see citing works
Iron uptake in fungi: a system for every source
Philpott, C. C. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2006.05.008 · Cited by 289 · see citing works
Romero‐Guido, C., Belo, I., Ta, T. M. N., Cao‐Hoang, L., Alchihab, M., Gomes, N., Thonart, P., Teixeira, J. A., Destain, J., & Waché, Y. (2010) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-010-2945-0 · Cited by 162 · see citing works
A Role for Sterol Levels in Oxygen Sensing in <i>Saccharomyces cerevisiae</i>
Davies, B. S. J., & Rine, J. (2006) · Genetics · doi:10.1534/genetics.106.059964 · Cited by 123 · see citing works
Znaidi, S., Weber, S., Zin Al-Abdin, O., Bomme, P., Saidane, S., Drouin, S., Lemieux, S., De Deken, X., Robert, F., & Raymond, M. (2008) · Eukaryotic Cell · doi:10.1128/ec.00070-08 · Cited by 119 · see citing works
Iron-dependent metabolic remodeling in S. cerevisiae
Kaplan, J., Ward, D. M., Crisp, R., & Philpott, C. C. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2006.03.008 · Cited by 120 · see citing works
Mechanisms of sterol uptake and transport in yeast
Jacquier, N., & Schneiter, R. (2010) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2010.11.014 · Cited by 115 · see citing works
Factors involved in anaerobic growth of Saccharomyces cerevisiae
Snoek, I. S. I., & Steensma, H. Y. (2006) · Yeast · doi:10.1002/yea.1430 · Cited by 99 · see citing works
Sterol transport in yeast and the oxysterol binding protein homologue (OSH) family
Schulz, T. A., & Prinz, W. A. (2007) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2007.03.003 · Cited by 91 · see citing works
Zavrel, M., Hoot, S. J., & White, T. C. (2013) · Eukaryotic Cell · doi:10.1128/ec.00345-12 · Cited by 86 · see citing works
Guzy, R. D., Mack, M. M., & Schumacker, P. T. (2007) · Antioxidants and Redox Signaling · doi:10.1089/ars.2007.1708 · Cited by 86 · see citing works
A Genomewide Screen Reveals a Role of Mitochondria in Anaerobic Uptake of Sterols in Yeast
Reiner, S., Micolod, D., Zellnig, G., & Schneiter, R. (2005) · Molecular Biology of the Cell · doi:10.1091/mbc.e05-06-0515 · Cited by 81 · see citing works
Snoek, I. S. I., & Steensma, H. Y. (2006) · FEMS Yeast Research · doi:10.1111/j.1567-1364.2005.00007.x · Cited by 80 · see citing works
Buechel, E. R., & Pinkett, H. W. (2020) · FEBS Letters · doi:10.1002/1873-3468.13964 · Cited by 70 · see citing works
Host-to-Pathogen Gene Transfer Facilitated Infection of Insects by a Pathogenic Fungus
Zhao, H. G., Xu, C., Lu, H., Chen, X., Leger, R. J. S., & Fang, W. (2014) · PLoS Pathogens · doi:10.1371/journal.ppat.1004009 · Cited by 73 · see citing works
Multiple roles of ABC transporters in yeast
Kumari, S., Kumar, M., Gaur, N. A., & Prasad, R. (2021) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2021.103550 · Cited by 66 · see citing works
Characteristics of Oxysterol Binding Proteins
Yan, D., & Olkkonen, V. M. (2008) · International review of cytology · doi:10.1016/s0074-7696(07)65007-4 · Cited by 66 · see citing works
Low oxygen levels as a trigger for enhancement of respiratory metabolism in Saccharomyces cerevisiae
Rintala, E., Toivari, M. H., Pitkänen, J., Wiebe, M. G., Ruohonen, L., & Penttilä, M. E. (2009) · BMC Genomics · doi:10.1186/1471-2164-10-461 · Cited by 65 · see citing works
Encapsulation in a natural, preformed, multi-component and complex capsule: yeast cells
Pham-Hoang, B. N., Romero‐Guido, C., Phan‐Thi, H., & Waché, Y. (2013) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-013-5044-1 · Cited by 63 · see citing works
Koselny, K., Mutlu, N., Minard, A. Y., Kumar, A., Krysan, D. J., & Wellington, M. A. (2018) · mBio · doi:10.1128/mbio.01204-18 · Cited by 60 · see citing works
Protein‐facilitated transport of hydrophobic molecules across the yeast plasma membrane
Claus, S., Jezierska, S., & Bogaert, I. V. (2019) · FEBS Letters · doi:10.1002/1873-3468.13469 · Cited by 58 · see citing works
The metabolism of lipids in yeasts and applications in oenology
Mbuyane, L. L., Bauer, F. F., & Divol, B. (2021) · Food Research International · doi:10.1016/j.foodres.2021.110142 · Cited by 54 · see citing works
Functional analyses of PAU genes in Saccharomyces cerevisiae
Luo, Z., & van Vuuren, H. J. J. (2009) · Microbiology · doi:10.1099/mic.0.030726-0 · Cited by 54 · see citing works
Transcriptome analysis of differential responses of diploid and haploid yeast to ethanol stress
Li, B., Cheng, J., Ding, M., & Yuan, Y. (2010) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2010.06.013 · Cited by 53 · see citing works
Kohút, P., Wüstner, D., Hronská, L., Kuchler, K., Hapala, I., & Valachovič, M. (2010) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2010.11.099 · Cited by 52 · see citing works
Sterol biosynthesis and sterol uptake in the fungal pathogen Pneumocystis carinii
Joffrion, T. M., & Cushion, M. T. (2010) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2010.02007.x · Cited by 48 · see citing works
Role of Heme in the Antifungal Activity of the Azaoxoaporphine Alkaloid Sampangine
Agarwal, A. K., Xu, T., Jacob, M. R., Feng, Q. F., Lorenz, M. C., Walker, L., & Clark, A. M. (2007) · Eukaryotic Cell · doi:10.1128/ec.00323-07 · Cited by 47 · see citing works
Leveraging transcription factors to speed cellobiose fermentation by Saccharomyces cerevisiae
Lin, Y., Chomvong, K., Acosta‐Sampson, L., Estrela, R., Galazka, J. M., Kim, S. R., Jin, Y., & Cate, J. H. D. (2014) · Biotechnology for Biofuels · doi:10.1186/s13068-014-0126-6 · Cited by 43 · see citing works
Joshua, I., & Höfken, T. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18040772 · Cited by 40 · see citing works
Engineering the thermotolerant industrial yeast Kluyveromyces marxianus for anaerobic growth
Dekker, W. J. C., Ortiz‐Merino, R. A., Kaljouw, A., Battjes, J., Wiering, F. W., Mooiman, C., Cortés, P. D. L. T., & Pronk, J. T. (2021) · Metabolic Engineering · doi:10.1016/j.ymben.2021.07.006 · Cited by 41 · see citing works
Piva, G. G., Casalta, E., Legras, J., Tesnière, C., Sablayrolles, J.-M., Ferreira, D., Ortiz-Julien, A., Galéote, V., & Mouret, J. (2022) · Fermentation · doi:10.3390/fermentation8020090 · Cited by 42 · see citing works
Evolutionary divergence in the fungal response to fluconazole revealed by soft clustering
Kuo, D., Tan, K., Zinman, G., Ravasi, T., Bar‐Joseph, Z., & Ideker, T. E. (2010) · Genome biology · doi:10.1186/gb-2010-11-7-r77 · Cited by 40 · see citing works
Importance and role of lipids in wine yeast fermentation
Tesnière, C. (2019) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-019-10029-4 · Cited by 41 · see citing works
Kuranda, K., François, J., & Palamarczyk, G. (2009) · FEMS Yeast Research · doi:10.1111/j.1567-1364.2009.00560.x · Cited by 40 · see citing works
The Yeast Plasma Membrane ATP Binding Cassette (ABC) Transporter Aus1
Marek, M., Milles, S., Schreiber, G., Daleke, D. L., Dittmar, G. A. G., Herrmann, A., Müller, P. K., & Pomorski, T. G. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.244525 · Cited by 39 · see citing works
The Structure and Function of the Yeast Cell Wall, Plasma Membrane and Periplasm
Stewart, G. G. (2017) · Springer eBooks · doi:10.1007/978-3-319-69126-8_5 · Cited by 35 · see citing works
Role of lipid transporters in fungal physiology and pathogenicity
Rizzo, J., Stanchev, L. D., Silva, V. K. A., Nimrichter, L., Pomorski, T. G., & Rodrigues, M. L. (2019) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2019.09.001 · Cited by 36 · see citing works
Nagi, M., Tanabe, K., Ueno, K., Nakayama, H., Aoyama, T., Chibana, H., Yamagoe, S., Umeyama, T., Oura, T., Ohno, H., et al. (2013) · Molecular Microbiology · doi:10.1111/mmi.12189 · Cited by 34 · see citing works
Serratore, N. D., Baker, K. M., Macadlo, L. A., Gress, A. R., Powers, B. L., Atallah, N., Westerhouse, K. M., Hall, M. C., Weake, V. M., & Briggs, S. D. (2018) · Genetics · doi:10.1534/genetics.117.300554 · Cited by 33 · see citing works
Ward, D. M., Chen, O. S., Li, L., Kaplan, J., Bhuiyan, S. A., Natarajan, S. K., Bard, M., & Cox, J. E. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.001781 · Cited by 32 · see citing works
Rintala, E., Jouhten, P., Toivari, M. H., Wiebe, M. G., Maaheimo, H., Penttilä, M. E., & Ruohonen, L. (2011) · OMICS A Journal of Integrative Biology · doi:10.1089/omi.2010.0082 · Cited by 32 · see citing works
Cell Surface Interference with Plasma Membrane and Transport Processes in Yeasts
François, J. (2015) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-25304-6_2 · Cited by 28 · see citing works
Sullivan, D. P., Georgiev, A. G., & Menon, A. K. (2008) · Eukaryotic Cell · doi:10.1128/ec.00135-08 · Cited by 28 · see citing works
Intracellular sterol transport in eukaryotes, a connection to mitochondrial function?
Schneiter, R. (2006) · Biochimie · doi:10.1016/j.biochi.2006.07.022 · Cited by 25 · see citing works
Lin, M., Unden, H., Jacquier, N., Schneiter, R., Just, U., & Höfken, T. (2009) · Molecular Biology of the Cell · doi:10.1091/mbc.e09-01-0034 · Cited by 24 · see citing works
Woods, K., & Höfken, T. (2015) · Molecular Microbiology · doi:10.1111/mmi.13244 · Cited by 23 · see citing works
Saccharomyces cerevisiae, a model to study sterol uptake and transport in eukaryotes
Micolod, D., Reiner, S., & Schneiter, R. (2005) · Biochemical Society Transactions · doi:10.1042/bst20051186 · Cited by 23 · see citing works
The Zinc Cluster Protein Sut1 Contributes to Filamentation in Saccharomyces cerevisiae
Foster, H. A., Cui, M., Naveenathayalan, A., Unden, H., Schwanbeck, R., & Höfken, T. (2012) · Eukaryotic Cell · doi:10.1128/ec.00214-12 · Cited by 21 · see citing works
Luo, Z., & van Vuuren, H. J. J. (2008) · FEMS Yeast Research · doi:10.1111/j.1567-1364.2008.00355.x · Cited by 19 · see citing works
Steroid toxicity and detoxification in ascomycetous fungi
Cvelbar, D., Žist, V., Kobal, K., Žigon, D., & Žakelj‐Mavrič, M. (2012) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2012.11.025 · Cited by 15 · see citing works
The yeast genome may harbor hypoxia response elements (HRE)
Ferreira, T. C., Hertzberg, L., Gassmann, M., & Campos, E. G. (2006) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cbpc.2006.08.013 · Cited by 13 · see citing works
Sterol Composition Modulates the Response of Saccharomyces cerevisiae to Iron Deficiency
Jordá, T., Rozés, N., & Puig, S. (2021) · Journal of Fungi · doi:10.3390/jof7110901 · Cited by 13 · see citing works
Serum cholesterol promotes the growth of Candida glabrata in the presence of fluconazole
Nagi, M., Tanabe, K., Yamagoe, S., Umeyama, T., Ohno, H., Miyazaki, Y., Nagi, M., Oura, T., Kajiwara, S., & Nakayama, H. (2012) · Journal of Infection and Chemotherapy · doi:10.1007/s10156-012-0531-3 · Cited by 13 · see citing works
Laub, K. R., Marek, M., Stanchev, L. D., Herrera, S. A., Kanashova, T., Bourmaud, A., Dittmar, G. A. G., & Pomorski, T. G. (2017) · PLoS ONE · doi:10.1371/journal.pone.0184236 · Cited by 12 · see citing works
Papay, M., Klein, C., Hapala, I., Petrisková, L., Kuchler, K., & Valachovič, M. (2019) · Yeast · doi:10.1002/yea.3456 · Cited by 10 · see citing works
Subtelomeric Regions Promote Evolutionary Innovation of Gene Families in Yeast
Snoek, T., Voordeckers, K., & Verstrepen, K. J. (2013) · Springer eBooks · doi:10.1007/978-3-642-41566-1_3 · Cited by 8 · see citing works
Blanda, C., & Höfken, T. (2013) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2013.07.027 · Cited by 10 · see citing works
The mannoprotein TIR3 (CAGL0C03872g) is required for sterol uptake in Candida glabrata
Inukai, T., Nagi, M., Morita, A., Tanabe, K., Aoyama, T., Miyazaki, Y., Bard, M., & Nakayama, H. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2014.11.002 · Cited by 8 · see citing works
Advances in biosynthesis of 7-Dehydrocholesterol through de novo cell factory strategies
Han, Y., Huang, Y., Israr, M., Li, H., & Zhang, W. (2024) · Bioresource Technology · doi:10.1016/j.biortech.2024.131888 · Cited by 9 · see citing works
Dekker, W. J. C., Juergens, H., Ortiz‐Merino, R. A., Mooiman, C., van den Berg, R., Kaljouw, A., Mans, R., & Pronk, J. T. (2022) · FEMS Yeast Research · doi:10.1093/femsyr/foac007 · Cited by 7 · see citing works
Genomics and Biodiversity in Yeasts
Bolotin‐Fukuhara, M. (2006) · Springer eBooks · doi:10.1007/3-540-30985-3_4 · Cited by 6 · see citing works
The evolution of anaerobic growth in Saccharomycotina yeasts
Krause, D. J. (2023) · Yeast · doi:10.1002/yea.3890 · Cited by 6 · see citing works
Ecm22 and Upc2 regulate yeast mating through control of expression of the mating genes PRM1 and PRM4
Höfken, T. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2017.10.005 · Cited by 5 · see citing works
Expression of the Cell Wall Mannoprotein GenesCWPandDANduring Industrial-Scale Lager Fermentations
Lawrence, S. J., Gibson, B. R., & Smart, K. A. (2009) · Journal of the American Society of Brewing Chemists · doi:10.1094/asbcj-2009-0114-01 · Cited by 5 · see citing works
Stanchev, L. D., Marek, M., Xian, F., Klöhn, M., Silvestro, D., Dittmar, G. A. G., López‐Marqués, R. L., & Pomorski, T. G. (2020) · Journal of Fungi · doi:10.3390/jof7010002 · Cited by 4 · see citing works
Wüstner, D. (2019) · Theoretical Biology and Medical Modelling · doi:10.1186/s12976-019-0108-2 · Cited by 3 · see citing works
Effects of oxygen provision on the physiology of baker's yeast Saccharomyces cerevisiae
Rintala, E. (2010) · Työväentutkimus Vuosikirja · Cited by 3 · see citing works
Rabies: risk, prognosis and prevention.
Driver, C. (2014) · PubMed · Cited by 2 · see citing works
Lawrence, S. J., & Smart, K. A. (2011) · Journal of the American Society of Brewing Chemists · doi:10.1094/asbcj-2011-0527-01 · Cited by 1 · see citing works
Identification and regulation of genes involved in anaerobic growth of Saccharomyces cerevisiae
Snoek, I. S. I. (2007) · Leiden Repository (Leiden University) · Cited by 1 · see citing works
Kuranda, K. (2006) · OpenGrey (Institut de l'Information Scientifique et Technique) · Cited by 1 · see citing works
Pineau, L. (2008) · OpenGrey (Institut de l'Information Scientifique et Technique)
Analysis of High Throughput Genomic Datasets Across Species
Zinman, G. (2012)
Etude des besoins en stérols des souches de levures œnologiques (Saccharomyces Cerevisiae)
Piva, G. G. (2022) · theses.fr (ABES) · doi:10.70675/8a3d39d9z1c93z47b6z900fz2213d379468e
Merber, R., Laczi, K., Bende, G., Kazinczi, E., Farkas, A., Maróti, G., Sinka, R., & Galgóczy, L. (2026) · Microbiology Spectrum · doi:10.1128/spectrum.00404-26
Saccharomyces cerevisiae, a model to study sterol uptake and transport in eukaryotes
Reiner, S., Micolod, D., & Schneiter, R. (2005) · Biochemical Society Transactions · doi:10.1042/bst0331186
Cui, M., Gao, X., Zhao, W., Wang, J., Wu, Y., & Zhang, X. (2026) · Journal of Fungi · doi:10.3390/jof12100795
Ferreira, T. C. (2006) · Americanae (AECID Library)
- Authors
- ALIMARDANI, P., RÉGNACQ, M., MOREAU-VAUZELLE, C., FERREIRA, T., ROSSIGNOL, T., BLONDIN, B., & BERGÈS, T.
- Affiliations
- Centre National de la Recherche Scientifique (FR)
- Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (FR)
- Corresponding author
- ALIMARDANI, Parissa
- FERREIRA, Thierry
- Venue
- Biochemical Journal
- Publisher
- Portland Press Ltd.
- Published
- 2004-06-22
- Volume
- 381
- Issue
- 1
- Pages
- 195-202
- ISSN
- 0264-6021 (ISSN-L)
- 1470-8728
- PMC
- PMC1133777
- OpenAlex
- W2013026032
- Cited by
- 84
- References
- 33
- Citations by year
- 2026: 2 · 2024: 1 · 2023: 1 · 2022: 4 · 2021: 4 · 2020: 4 · 2019: 5 · 2018: 3 · 2017: 5 · 2015: 2 · 2014: 4 · 2013: 5 · 2012: 5
- FWCI
- 2.14
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Biochemical Journal (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Health Sciences › Medicine › Surgery › Cholesterol and Lipid Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Lipid metabolism and biosynthesis
- Keywords
- sterol uptake, SUT1, ABC transporters, mannoproteins, Saccharomyces cerevisiae, transcription factors, cell wall
- MeSH terms
- Aerobiosis, DNA-Binding Proteins, Glycoproteins, Membrane Glycoproteins, Microtubule-Associated Proteins, Repressor Proteins, Saccharomyces cerevisiae, Species Specificity, Sterols, Transcription, Genetic, Trans-Activators, Gene Expression Regulation, Fungal, Genome, Fungal, ATP-Binding Cassette Transporters, Oligonucleotide Array Sequence Analysis, Gene Expression Profiling, Saccharomyces cerevisiae Proteins
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