The DOI matches its Crossref record; 61 of the 62 references it cites were found in a registry or an index.
Calcineurin-dependent regulation of Crz1p nuclear export requires Msn5p and a conserved calcineurin docking site
Open accessAbstract
Calcineurin, a conserved Ca 2+/calmodulin-regulated protein phosphatase, plays a crucial role in Ca 2+ signaling in a wide variety of cell types. In Saccharomyces cerevisiae, calcineurin positively regulates transcription in response to stress by dephosphorylating the transcription factor Crz1p/Tcn1p. Dephosphorylation promotes Crz1p nuclear localization in part by increasing the efficiency of its nuclear import. In this work, we show that calcineurin-dependent dephosphorylation of Crz1p also down-regulates its nuclear export. Using a genetic approach, we identify Msn5p as the exportin for Crz1p. In addition, we define the Crz1p nuclear export signal (NES) and show that it interacts with Msn5p in a phosphorylation-dependent manner. This indicates that calcineurin regulates Crz1p nuclear export by dephosphorylating and inactivating its NES. Finally, we define a motif in Crz1p, PIISIQ, similar to the PxIxIT docking site for calcineurin on the mammalian transcription factor NFAT, that mediates the in vivo interaction between calcineurin and Crz1p and is required for calcineurin-dependent regulation of Crz1p nuclear export and activity. Therefore, in yeast as in mammals, a docking site is required to target calcineurin to its substrate such that it can dephosphorylate it efficiently.
Overview
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
Verification
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?
In the citing paper
“much likely the cell components involved in this nucleo-cytoplasmic shuffling, which have been already identified in S. cerevisiae (Polizotto and Cyert 2001;Boustany and Cyert 2002), are conserved in C. albicans.”
From Functional characterization of the Candida albicans CRZ1 gene encoding a calcineurin-regulated transcription factor (2005) · cites this paper as Boustany and Cyert 2002
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Calcium's Role in Mechanotransduction during Muscle Development
Damm, T. B., & Egli, M. (2014) · Cellular Physiology and Biochemistry · doi:10.1159/000356667 · Cited by 14,552
Sikorski, R. S., & Hieter, P. (1989) · Genetics · doi:10.1093/genetics/122.1.19 · Cited by 8,590
Sherman, F., Fink, G. R., & Hicks, J. B. (1979) · Cold Spring Harbor Laboratory eBooks · Cited by 7,430
Cold Spring Harbor Laboratory; Cold Spring Harbor, NY
Cavalier-Smith, T. (1980) · FEBS Letters · doi:10.1016/0014-5793(80)80323-1 · Cited by 6,317
Calcineurin is a common target of cyclophilin-cyclosporin A and FKBP-FK506 complexes
Liu, J., Farmer, J. D., Lane, W. S., Friedman, J., Weissman, I., & Schreiber, S. L. (1991) · Cell · doi:10.1016/0092-8674(91)90124-h · Cited by 4,116
Genomic Libraries and a Host Strain Designed for Highly Efficient Two-Hybrid Selection in Yeast
James, P. M., Halladay, J. T., & Craig, E. A. (1996) · Genetics · doi:10.1093/genetics/144.4.1425 · Cited by 2,638
A Calcineurin-Dependent Transcriptional Pathway for Cardiac Hypertrophy
Molkentin, J. D., Lu, J., Antos, C. L., Markham, B. E., Richardson, J. A., Robbins, J. M., Grant, S. R., & Olson, E. N. (1998) · Cell · doi:10.1016/s0092-8674(00)81573-1 · Cited by 2,566
A short amino acid sequence able to specify nuclear location
Kalderon, D., Roberts, B., Richardson, W. D., & Smith, A. E. (1984) · Cell · doi:10.1016/0092-8674(84)90457-4 · Cited by 2,511
CRM1 Is an Export Receptor for Leucine-Rich Nuclear Export Signals
Fornerod, M. W. J., Ohno, M., Yoshida, M., & Mattaj, I. W. (1997) · Cell · doi:10.1016/s0092-8674(00)80371-2 · Cited by 2,086
A new efficient gene disruption cassette for repeated use in budding yeast
Güldener, U. (1996) · Nucleic Acids Research · doi:10.1093/nar/24.13.2519 · Cited by 1,657
Research works printed but not linked: 2
- Ausubel F.M. Brent R. Kingston R.E. Moore D.D. Seidman J.G. Smith J.A. Struhl K. (1987) Current protocols in molecular biology. (John Wiley, New York, NY).
- Stathopoulos A.M. (1998) “Calcineurin regulates the CRZ1 transcription factor to control gene expression in Saccharomyces cerevisiae .” Ph.D. thesis (Stanford University, Stanford, CA).
Cited by
Sorted by citations
Mapping Pathways and Phenotypes by Systematic Gene Overexpression
Sopko, R., Huang, D., Preston, N., Chua, G., Papp, B., Kafadar, K. A., Snyder, M., Oliver, S. G., Cyert, M., Hughes, T. R., et al. (2006) · Molecular Cell · doi:10.1016/j.molcel.2005.12.011 · Cited by 669
Self-citationNucleocytoplasmic transport: taking an inventory
Fried, H. M., & Kutay, U. (2003) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-003-3070-3 · Cited by 515
Regulation of Cell Cycle Progression by Calcium/Calmodulin-Dependent Pathways
Kahl, C. R., & Means, A. R. (2003) · Endocrine Reviews · doi:10.1210/er.2003-0008 · Cited by 493
Frequency-modulated nuclear localization bursts coordinate gene regulation
Cai, L., Dalal, C. K., & Elowitz, M. B. (2008) · Nature · doi:10.1038/nature07292 · Cited by 492
Yoshimoto, H., Saltsman, K., Gasch, A. P., Li, H. X., Ogawa, N., Botstein, D., Brown, P. O., & Cyert, M. S. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m202718200 · Cited by 404
Self-citationInteraction of calcineurin with substrates and targeting proteins
Li, H., Rao, A., & Hogan, P. G. (2010) · Trends in Cell Biology · doi:10.1016/j.tcb.2010.09.011 · Cited by 381
Regulation of Nuclear Transport: Central Role in Development and Transformation?
Poon, I. K. H., & Jans, D. A. (2005) · Traffic · doi:10.1111/j.1600-0854.2005.00268.x · Cited by 360
Sanglard, D., Ischer, F., Marchetti, O., Entenza, J., & Bille, J. (2003) · Molecular Microbiology · doi:10.1046/j.1365-2958.2003.03495.x · Cited by 350
Calcineurin signaling in Saccharomyces cerevisiae: how yeast go crazy in response to stress.
Cyert, M. S. (2003) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(03)01552-3 · Cited by 333
Self-citationKaryopherins: from nuclear-transport mediators to nuclear-function regulators
Mosammaparast, N., & Pemberton, L. F. (2004) · Trends in Cell Biology · doi:10.1016/j.tcb.2004.09.004 · Cited by 316
Harnessing calcineurin as a novel anti-infective agent against invasive fungal infections.
Steinbach, W. J., Reedy, J. L., Cramer, R. A., Perfect, J. R., & Heitman, J. (2007) · Nature Reviews Microbiology · doi:10.1038/nrmicro1680 · Cited by 313
HASTY, theArabidopsisortholog of exportin 5/MSN5, regulates phase change and morphogenesis
Bollman, K. M., Aukerman, M. J., Park, M., Hunter, C., Berardini, T., & Poethig, R. S. (2003) · Development · doi:10.1242/dev.00362 · Cited by 290
CRZ1 , a target of the calcineurin pathway in Candida albicans
Karababa, M., Valentino, E., Pardini, G., Coste, A. T., Bille, J., & Sanglard, D. (2006) · Molecular Microbiology · doi:10.1111/j.1365-2958.2005.05037.x · Cited by 231
Short linear motifs – ex nihilo evolution of protein regulation
Davey, N. E., Cyert, M., & Moses, A. M. (2015) · Cell Communication and Signaling · doi:10.1186/s12964-015-0120-z · Cited by 228
Self-citationLife in the midst of scarcity: adaptations to nutrient availability in Saccharomyces cerevisiae
Smets, B., Ghillebert, R., Snijder, P. D., Binda, M., Swinnen, E., VIRGILIO, C. D., & Winderickx, J. (2010) · Current Genetics · doi:10.1007/s00294-009-0287-1 · Cited by 216
Ca2+/calcineurin signalling in cells of the immune system
Feske, S., Okamura, H., Hogan, P. G., & Rao, A. (2003) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2003.09.174 · Cited by 181
Cramer, R. A., Perfect, B. Z., Pinchai, N., Park, S., Perlin, D. S., Asfaw, Y. G., Heitman, J., Perfect, J. R., & Steinbach, W. J. (2008) · Eukaryotic Cell · doi:10.1128/ec.00086-08 · Cited by 172
Coping with stress: calmodulin and calcineurin in model and pathogenic fungi
Kraus, P. R., & Heitman, J. (2003) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(03)01528-6 · Cited by 169
Cracking the Phosphatase Code: Docking Interactions Determine Substrate Specificity
Roy, J., & Cyert, M. (2009) · Science Signaling · doi:10.1126/scisignal.2100re9 · Cited by 164
Self-citationCalcineurin-Crz1 Signaling in Lower Eukaryotes
Thewes, S. (2014) · Eukaryotic Cell · doi:10.1128/ec.00038-14 · Cited by 157
Nuclear Export Signal Consensus Sequences Defined Using a Localization‐Based Yeast Selection System
Kosugi, S., Hasebe, M., Tomita, M., & Yanagawa, H. (2008) · Traffic · doi:10.1111/j.1600-0854.2008.00825.x · Cited by 141
Tabuchi, M., Audhya, A., Parsons, A. B., Boone, C. M., & Emr, S. D. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.02403-05 · Cited by 134
Li, H., Zhang, L., Rao, A., Harrison, S. C., & Hogan, P. G. (2007) · Journal of Molecular Biology · doi:10.1016/j.jmb.2007.04.032 · Cited by 133
Choi, J., Kim, Y., Kim, S., Park, J., & Lee, Y. (2008) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2008.11.010 · Cited by 131
Roetzer, A., Gregori, C., Jennings, A. M., Quintin, J., Ferrandon, D., Butler, G., Kuchler, K., Ammerer, G., & Schüller, C. (2008) · Molecular Microbiology · doi:10.1111/j.1365-2958.2008.06301.x · Cited by 124
Onyewu, C., Wormley, F. L., Perfect, J. R., & Heitman, J. (2004) · Infection and Immunity · doi:10.1128/iai.72.12.7330-7333.2004 · Cited by 121
Acidic calcium stores of Saccharomyces cerevisiae
Cunningham, K. W. (2011) · Cell Calcium · doi:10.1016/j.ceca.2011.01.010 · Cited by 120
Maeta, K., Izawa, S., & Inoue, Y. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m408061200 · Cited by 118
Spielvogel, A., Findon, H., Arst, H. N., Araújo‐Bazán, L., Hernández-Ortíz, P., Ståhl, U., Meyer, V., & Espeso, E. A. (2008) · Biochemical Journal · doi:10.1042/bj20080344 · Cited by 108
Bultynck, G., Heath, V., Majeed, A. P., Galan, J., Haguenauer-Tsapis, R., & Cyert, M. S. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.01973-05 · Cited by 115
Self-citationMohl, D. A., Huddleston, M. J., Collingwood, T. S., Annan, R. S., & Deshaies, R. J. (2009) · The Journal of Cell Biology · doi:10.1083/jcb.200812022 · Cited by 108
Santhanam, A. N., Hartley, A. D., Düvel, K., Broach, J. R., & Garrett, S. (2004) · Eukaryotic Cell · doi:10.1128/ec.3.5.1261-1271.2004 · Cited by 107
Merkle, T. (2003) · Current Genetics · doi:10.1007/s00294-003-0444-x · Cited by 102
Roy, J., Li, H., Hogan, P. G., & Cyert, M. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.02.014 · Cited by 101
Self-citationChow, E. W. L., Clancey, S. A., Billmyre, R. B., Averette, A. F., Granek, J. A., Mieczkowski, P. A., Cardenas, M. E., & Heitman, J. (2017) · PLoS Genetics · doi:10.1371/journal.pgen.1006667 · Cited by 100
Czirják, G., & Enyedi, P. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m602495200 · Cited by 97
Ueta, R., Fujiwara, N., Iwaï, K., & Yamaguchi‐Iwai, Y. (2007) · Molecular Biology of the Cell · doi:10.1091/mbc.e06-11-1054 · Cited by 90
Lev, S., Desmarini, D., Chayakulkeeree, M., Sorrell, T. C., & Djordjevic, J. T. (2012) · PLoS ONE · doi:10.1371/journal.pone.0051403 · Cited by 85
Kafadar, K. A., & Cyert, M. (2004) · Eukaryotic Cell · doi:10.1128/ec.3.5.1147-1153.2004 · Cited by 85
Self-citationNegative regulation of calcineurin signaling by Hrr25p, a yeast homolog of casein kinase IPreprint
Kafadar, K. A., Zhu, H., Snyder, M. P., & Cyert, M. (2003) · Genes & Development · doi:10.1101/gad.1140603 · Cited by 84
Self-citationExportin-5 orthologues are functionally divergent among species
Shibata, S., Sasaki, M., Miki, T., Shimamoto, A., Furuichi, Y., Katahira, J., & Yoneda, Y. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl663 · Cited by 83
Li, H., Rao, A., & Hogan, P. G. (2004) · Journal of Molecular Biology · doi:10.1016/j.jmb.2004.07.068 · Cited by 82
Santos, M., & de Larrinoa, I. F. (2005) · Current Genetics · doi:10.1007/s00294-005-0003-8 · Cited by 78
Ueta, R., Fujiwara, N., Iwai, K., & Yamaguchi-Iwai, Y. (2012) · Molecular and Cellular Biology · doi:10.1128/mcb.00726-12 · Cited by 78
Adaptation to environmental pH: integrating the Rim101 and calcineurin signal transduction pathways
Kullas, A. L., Martin, S. J., & Davis, D. (2007) · Molecular Microbiology · doi:10.1111/j.1365-2958.2007.05929.x · Cited by 75
The role of karyopherins in the regulated sumoylation of septins
Makhnevych, T., Ptak, C. P., Lusk, C. P., Aitchison, J. D., & Wozniak, R. W. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200608066 · Cited by 73
Kim, S. J., Ding, W., Albrecht, B., Green, P. L., & Lairmore, M. D. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m210210200 · Cited by 71
Hagiwara, D., Kondo, A., Fujioka, T., & Abe, K. (2008) · Current Genetics · doi:10.1007/s00294-008-0220-z · Cited by 69
Heath, V. L., Shaw, S. L., Roy, S., & Cyert, M. (2004) · Eukaryotic Cell · doi:10.1128/ec.3.3.695-704.2004 · Cited by 68
Self-citationWhi5 Regulation by Site Specific CDK-Phosphorylation in Saccharomyces cerevisiae
Wagner, M. V., Smolka, M. B., de Bruin, R. A. M., Zhou, H., Wittenberg, C., & Dowdy, S. F. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004300 · Cited by 67
Tucker, S. L., Besi, M. I., Galhano, R., Franceschetti, M., Goetz, S., Lenhert, S., Osbourn, A., & Sesma, A. (2010) · The Plant Cell · doi:10.1105/tpc.109.066340 · Cited by 67
Hernández-Ortíz, P., & Espeso, E. A. (2013) · Molecular Microbiology · doi:10.1111/mmi.12294 · Cited by 62
Direct Regulation of Genes Involved in Glucose Utilization by the Calcium/Calcineurin Pathway
Ruiz, A., Serrano, R., & Ariño, J. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m708683200 · Cited by 60
Towpik, J., Graczyk, D., Gajda, A. E., Lefebvre, O., & Boguta, M. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m709157200 · Cited by 59
A Calcineurin-dependent Switch Controls the Trafficking Function of α-Arrestin Aly1/Art6
O’Donnell, A. F., Huang, L., Thorner, J. W., & Cyert, M. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.478511 · Cited by 58
Self-citationGenetic Factors That Regulate the Attenuation of the General Stress Response of Yeast
Bose, S., Dutko, J. A., & Zitomer, R. S. (2004) · Genetics · doi:10.1534/genetics.104.034603 · Cited by 49
SUMO and Nucleocytoplasmic Transport
Ptak, C. P., & Wozniak, R. W. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-50044-7_7 · Cited by 48
Adler, A., Park, Y., Larsen, P. E., Nagarajan, V., Wollenberg, K. R., Qiu, J. F., Myers, T. G., & Williamson, P. R. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.230268 · Cited by 48
Cell Cycle Activation of the Swi6p Transcription Factor Is Linked to Nucleocytoplasmic Shuttling
Queralt, E., & Igual, J. C. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.9.3126-3140.2003 · Cited by 48
Mathematical modeling of calcium homeostasis in yeast cells
Cui, J., & Kaandorp, J. A. (2006) · Cell Calcium · doi:10.1016/j.ceca.2005.12.001 · Cited by 47
Fox, D. S., Cox, G. M., & Heitman, J. (2003) · Eukaryotic Cell · doi:10.1128/ec.2.5.1025-1035.2003 · Cited by 47
Tisi, R., Rigamonti, M. M., Groppi, S., & Belotti, F. (2016) · AIMS molecular science · doi:10.3934/molsci.2016.4.505 · Cited by 41
Yang, Y. Y., Xie, P., Li, Y., Bi, Y., & Prusky, D. (2022) · Journal of Fungi · doi:10.3390/jof8101082 · Cited by 39
On the Roles of Calcineurin in Fungal Growth and Pathogenesis
Chen, Y., Kozubowski, L., Cardenas, M. E., & Heitman, J. (2010) · Current Fungal Infection Reports · doi:10.1007/s12281-010-0027-5 · Cited by 39
Bodvard, K., Jörhov, A., Blomberg, A., Molin, M., & Käll, M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0053404 · Cited by 39
A small molecule‐directed approach to control protein localization and function
Geda, P., Patury, S., Ma, J., Bharucha, N., Dobry, C. J., Lawson, S. K., Gestwicki, J. E., & Kumar, A. (2008) · Yeast · doi:10.1002/yea.1610 · Cited by 38
Sugiyama, M., 赤瀬, 晋., Nakanishi, R., Horie, H., Kaneko, Y., & Harashima, S. (2014) · Applied and Environmental Microbiology · doi:10.1128/aem.04241-13 · Cited by 39
Petrezsélyová, S., López‐Malo, M., Canadell, D., Roque, A., Serra‐Cardona, A., Marqués, M. C., Vilaprinyó, E., Alves, R., Yenush, L., & Ariño, J. (2016) · PLoS ONE · doi:10.1371/journal.pone.0158424 · Cited by 34
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
Espeso, E. A. (2016) · Advances in Experimental Medicine and Biology · doi:10.1007/978-3-319-25304-6_7 · Cited by 33
Quan, X., Tsoulos, P., Kuritzky, A., Zhang, R., & Stochaj, U. (2006) · Molecular Microbiology · doi:10.1111/j.1365-2958.2006.05395.x · Cited by 33
Regulation of Salt Tolerance byTorulaspora delbrueckiiCalcineurin Target Crz1p
Hernandez-Lopez, M., Panadero, J., Prieto, J. A., & Rández‐Gil, F. (2006) · Eukaryotic Cell · doi:10.1128/ec.5.3.469-479.2006 · Cited by 31
Regulation of developmental transitions
Chuck, G. S., & Hake, S. (2004) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2004.11.002 · Cited by 31
Koike, A., Kato, T., Sugiura, R., Ma, Y., Tabata, Y., Ohmoto, K., Sio, S. O., & Kuno, T. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.310615 · Cited by 25
Tsuzi, D., Maeta, K., Takatsume, Y., Izawa, S., & Inoue, Y. (2004) · FEBS Letters · doi:10.1016/j.febslet.2004.05.077 · Cited by 25
Dubey, A. K., Barad, S., Luria, N., Kumar, D., Espeso, E. A., & Prusky, D. (2016) · PLoS ONE · doi:10.1371/journal.pone.0168561 · Cited by 24
Takatsume, Y., Ohdate, T., Maeta, K., Nomura, W., Izawa, S., & Inoue, Y. (2010) · Biochemical Journal · doi:10.1042/bj20091334 · Cited by 23
Dual control by Cdk1 phosphorylation of the budding yeast APC/C ubiquitin ligase activator Cdh1
Höckner, S., Neumann-Arnold, L., & Seufert, W. (2016) · Molecular Biology of the Cell · doi:10.1091/mbc.e15-11-0787 · Cited by 22
Kap120 Functions as a Nuclear Import Receptor for Ribosome Assembly Factor Rpf1 in Yeast
Caesar, S., Greiner, M., & Schlenstedt, G. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.26.8.3170-3180.2006 · Cited by 22
Collins, M. E., Black, J. J., & Liu, Z. (2017) · Applied and Environmental Microbiology · doi:10.1128/aem.00672-17 · Cited by 22
Klee, C. B., & Means, A. R. (2002) · EMBO Reports · doi:10.1093/embo-reports/kvf182 · Cited by 17
The Ca2+–calcineurin–NFAT signalling pathway
Feske, S., Rao, A., & Hogan, P. G. (2007) · New comprehensive biochemistry · doi:10.1016/s0167-7306(06)41014-0 · Cited by 18
CRZ1 transcription factor is involved in cell survival, stress tolerance, and virulence in fungi
Gupta, S., Kumar, A., & Tamuli, R. (2022) · Journal of Biosciences · doi:10.1007/s12038-022-00294-3 · Cited by 17
Hsu, I. S., Strome, B., Lash, E., Robbins, N., Cowen, L. E., & Moses, A. M. (2021) · PLoS Genetics · doi:10.1371/journal.pgen.1009629 · Cited by 17
The CRZ1 transcription factor in plant fungi: regulation mechanism and impact on pathogenesis
Cacciotti, A., Beccaccioli, M., & Reverberi, M. (2024) · Molecular Biology Reports · doi:10.1007/s11033-024-09593-4 · Cited by 15
Jee, C., Choi, T.-W., Kalichamy, K., Yee, J. Z., Song, H., Ji, Y. J., Lee, J., Lee, J. I., L’Étoile, N. D., Ahnn, J., et al. (2012) · Journal of Molecular Biology · doi:10.1016/j.jmb.2012.01.012 · Cited by 14
Nuclear export of Ho endonuclease of yeast via Msn5
Bakhrat, A., Baranes‐Bachar, K., Reshef, D., Voloshin, O., Krichevsky, O., & Raveh, D. (2008) · Current Genetics · doi:10.1007/s00294-008-0216-8 · Cited by 15
An age-dependent feedback control model of calcium dynamics in yeast cells
Tang, F., & Liu, W. (2009) · Journal of Mathematical Biology · doi:10.1007/s00285-009-0289-0 · Cited by 13
Barroso, E. C., Yance-Chávez, T., Kito, A., Sugiura, R., Gómez-Hierro, A., Giménez-Zaragoza, D., & Aligué, R. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku684 · Cited by 12
Molecular basis of the functional distinction between Cln1 and Cln2 cyclins
Quilis, I., & Igual, J. C. (2012) · Cell Cycle · doi:10.4161/cc.21505 · Cited by 11
Belanger, K. D., Griffith, A. L., Baker, H. L., Hansen, J. N., Kovacs, L. A. S., Seconi, J. S., & Strine, A. C. (2011) · DNA and Cell Biology · doi:10.1089/dna.2010.1071 · Cited by 11
Belanger, K. D., Simmons, L. A., Roth, J. K., VanderPloeg, K. A., Lichten, L., & Fahrenkrog, B. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m407641200 · Cited by 11
Regulation of cell cycle transcription factor Swi5 by karyopherin Msn5
Taberner, F. J., Quilis, I., Sendra, J., Bañó, M. C., & Igual, J. C. (2012) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2012.02.009 · Cited by 10
Expression of the yeast calcineurin subunitsCNA1andCNA2during growth and hyper-osmotic stress
Aguila, E. M. D., Silva, J. T., & Paschoalin, V. M. F. (2003) · FEMS Microbiology Letters · doi:10.1016/s0378-1097(03)00181-2 · Cited by 10
Zhao, K., Liu, Z., Li, M., Hu, Y., Yang, L., Song, X., & Qin, Y. (2021) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2021.103652 · Cited by 9
Genetic Bypass of Aspergillus nidulans crzA Function in Calcium Homeostasis
Almeida, R. S., Loss, O., Colabardini, A. C., Brown, N. A., Bignell, E., Savoldi, M., Pantano, S., Goldman, M. H. S., Arst, H. N., & Goldman, G. H. (2013) · G3 Genes Genomes Genetics · doi:10.1534/g3.113.005983 · Cited by 10
Chawla, S., Ahmadpour, D., Schneider, K. L., Kumar, N., Fischbach, A., Molin, M., & Nyström, T. (2023) · Cell Communication and Signaling · doi:10.1186/s12964-023-01242-w · Cited by 9
A subset of FG-nucleoporins is necessary for efficient Msn5-mediated nuclear protein export
Finn, E. M., DeRoo, E., Clement, G. W., Rao, S., Kruse, S. E., Kokanovich, K. M., & Belanger, K. D. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2012.12.020 · Cited by 8
Cyert, M., Goldman, A. R., Roy, J., Bodenmiller, B., Wanka, S., Landry, C. R., & Aebersold, R. H. (2014) · The FASEB Journal · doi:10.1096/fasebj.28.1_supplement.586.3 · Cited by 6
Self-citationPhosphate-dependent nuclear export via a non-classical NES class recognized by exportin Msn5
Fung, H. Y. J., Mittal, S. R., Niesman, A. B., Jiou, J., Shakya, B., Yoshizawa, T., Cansizoglu, A. E., Rout, M. P., & Chook, Y. M. (2025) · Nature Communications · doi:10.1038/s41467-025-57752-3 · Cited by 5
Metadata
- Authors
- Boustany, L. M., & Cyert, M. S.
- Affiliations
- Stanford University (US)
- Venue
- Genes & Development
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2002-03-01
- Volume
- 16
- Issue
- 5
- Pages
- 608-619
- ISSN
- 0890-9369 (ISSN-L)
- 1549-5477
- PMC
- PMC155349
- OpenAlex
- W2110510554
- Cited by
- 115
- References
- 62
- Citations by year
- 2025: 1 · 2024: 1 · 2023: 1 · 2022: 2 · 2021: 3 · 2019: 1 · 2017: 3 · 2016: 7 · 2015: 4 · 2014: 6 · 2013: 5 · 2012: 6
- Type
- posted content
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Genes & Development (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Institute of General Medical Sciences (5 T32 GM07276, GM-48729, T32GM007276, R01GM048729)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Signaling Pathways in Disease
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nuclear Structure and Function
- Keywords
- calcineurin, nuclear export, nuclear export signal, protein dephosphorylation, NFAT, transcription factor regulation, Ca2+/calmodulin signaling, Saccharomyces cerevisiae, exportins
- MeSH terms
- Binding Sites, Carrier Proteins, Cell Nucleus, DNA-Binding Proteins, Mutation, Protein Binding, Saccharomyces cerevisiae, Transcription Factors, Trans-Activators, Conserved Sequence, Sequence Deletion, Calcineurin, Amino Acid Motifs, Protein Sorting Signals, Active Transport, Cell Nucleus, Karyopherins, 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