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Apical Sterol-rich Membranes Are Essential for Localizing Cell End Markers That Determine Growth Directionality in the Filamentous Fungus Aspergillus nidulans
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In filamentous fungi, hyphal extension depends on the continuous delivery of vesicles to the growing tip. Here, we describe the identification of two cell end marker proteins, TeaA and TeaR, in Aspergillus nidulans, corresponding to Tea1 and Mod5 in Schizosaccharomyces pombe. Deletion of teaA or teaR caused zig-zag-growing and meandering hyphae, respectively. The Kelch-repeat protein TeaA, the putatively prenylated TeaR protein, and the formin SepA were highly concentrated in the Spitzenkörper, a vesicle transit station at the tip, and localized along the tip membrane. TeaA localization at tips depended on microtubules, and TeaA was required for microtuble convergence in the hyphal apex. The CENP-E family kinesin KipA was necessary for proper localization of TeaA and TeaR, but not for their transportation. TeaA and TeaR localization were interdependent. TeaA interacted in vivo with TeaR, and TeaA colocalized with SepA. Sterol-rich membrane domains localized at the tip in teaA and teaR mutants like in wild type, and filipin treatment caused mislocalization of both proteins. This suggests that sterol-rich membrane domains determine cell end factor destinations and thereby polarized growth.
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“Interestingly, Takeshita et al. (2008) recently observed that localization of key deposition proteins involved in polarized growth at the hyphal tip requires apical sterol-rich membranes [52].”
From A Sterol-Regulatory Element Binding Protein Is Required for Cell Polarity, Hypoxia Adaptation, Azole Drug Resistance, and Virulence in Aspergillus fumigatus (2008) · cites this paper as [52]
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Cites
Molecular cloning: A laboratory manual
Deininger, P. L. (1990) · Analytical Biochemistry · doi:10.1016/0003-2697(90)90595-z · Cited by 84,684
Transformation of Aspergillus nidulans by using a trpC plasmid.
Yelton, M., Hamer, J. E., & Timberlake, W. E. (1984) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.81.5.1470 · Cited by 782
Adaptation of core mechanisms to generate cell polarity
Nelson, W. J. (2003) · Nature · doi:10.1038/nature01602 · Cited by 716
The Ashbya gossypii Genome as a Tool for Mapping the Ancient Saccharomyces cerevisiae Genome
Dietrich, F. S., Voegeli, S., Brachat, S., Lerch, A., Gates, K., Steiner, S., Mohr, C., Pöhlmann, R., Luedi, P. P., Choi, S., et al. (2004) · Science · doi:10.1126/science.1095781 · Cited by 633
Lipid rafts and membrane dynamics
Rajendran, L., & Simons, K. (2005) · Journal of Cell Science · doi:10.1242/jcs.01681 · Cited by 590
Rothberg, K. G., Ying, Y. S., Kamen, B. A., & Anderson, R. G. W. (1990) · The Journal of Cell Biology · doi:10.1083/jcb.111.6.2931 · Cited by 532
Protoplasmic organization of hyphal tips among fungi: vesicles and Spitzenkorper.
Grove, S. N., & Bracker, C. E. (1970) · Journal of Bacteriology · doi:10.1128/jb.104.2.989-1009.1970 · Cited by 432
Fischer-Parton, S., Parton, R. M., Hickey, P. C., Dijksterhuis, J., Atkinson, H. A., & Read, N. D. (2000) · Journal of Microscopy · doi:10.1046/j.1365-2818.2000.00708.x · Cited by 422
Mata, J., & Nurse, P. (1997) · Cell · doi:10.1016/s0092-8674(00)80279-2 · Cited by 353
Hill, T. W., & Käfer, E. (2001) · Fungal Genetics Reports · doi:10.4148/1941-4765.1173 · Cited by 349
Research works printed but not linked: 2
- Hill T. W., 2001, Fungal Genet. Newsl, 48, 20
- Riquelme M., 1998, Biol, 24, 101
Cited by
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Riquelme, M., Aguirre, J., Bartnicki-Garcı́a, S., Braus, G. H., Feldbrügge, M., Fleig, U. N., Hansberg, W., Herrera‐Estrella, A., Kämper, J., Kück, U., et al. (2018) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00068-17 · Cited by 403
Self-citationWillger, S. D., Puttikamonkul, S., Kim, K.-H., Burritt, J. B., Grahl, N., Metzler, L. J., Barbuch, R., Bard, M., Lawrence, C. B., & Cramer, R. A. (2008) · PLoS Pathogens · doi:10.1371/journal.ppat.1000200 · Cited by 345
Fischer, R., Zekert, N., & Takeshita, N. (2008) · Molecular Microbiology · doi:10.1111/j.1365-2958.2008.06193.x · Cited by 220
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Berepiki, A., Lichius, A., & Read, N. (2011) · Nature Reviews Microbiology · doi:10.1038/nrmicro2666 · Cited by 181
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Brand, A., & Gow, N. A. R. (2009) · Current Opinion in Microbiology · doi:10.1016/j.mib.2009.05.007 · Cited by 170
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Lara‐Rojas, F., Sánchez, O., Kawasaki, L., & Aguirre, J. (2011) · Molecular Microbiology · doi:10.1111/j.1365-2958.2011.07581.x · Cited by 156
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Takemoto, D., Kamakura, S., Saikia, S., Becker, Y., Wrenn, R. E., Tanaka, A., Sumimoto, H., & Scott, B. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1017309108 · Cited by 132
Aparicio, J. F., Barreales, E. G., Payero, T. D., Vicente, C. M., de Pedro, A., & Santos‐Aberturas, J. (2015) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-015-7077-0 · Cited by 124
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Thomson, D. D., Wehmeier, S., Byfield, F. J., Janmey, P. A., Caballero-Lima, D., Crossley, A., & Brand, A. C. (2015) · Cellular Microbiology · doi:10.1111/cmi.12369 · Cited by 81
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Brand, A., Lee, K., Veses, V., & Gow, N. A. R. (2009) · Molecular Microbiology · doi:10.1111/j.1365-2958.2008.06592.x · Cited by 71
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Takeshita, N. (2016) · Bioscience Biotechnology and Biochemistry · doi:10.1080/09168451.2016.1179092 · Cited by 72
Self-citationCarreras-Villaseñor, N., Naranjo, E. U. E., Villalobos‐Escobedo, J. M., Abreu‐Goodger, C., & Herrera‐Estrella, A. (2013) · Molecular Microbiology · doi:10.1111/mmi.12261 · Cited by 65
Seiler, S., & Justa‐Schuch, D. (2010) · Molecular Microbiology · doi:10.1111/j.1365-2958.2010.07392.x · Cited by 63
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Pöhlmann, J., Risse, C., Seidel, C., Pohlmann, T., Jakopec, V., Walla, E., Ramrath, P., Takeshita, N., Baumann, S. J., Feldbrügge, M., et al. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004586 · Cited by 56
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Schultzhaus, Z. S., & Shaw, B. D. (2015) · Fungal Biology Reviews · doi:10.1016/j.fbr.2015.04.002 · Cited by 48
Higashitsuji, Y., Herrero, S., Takeshita, N., & Fischer, R. (2009) · Eukaryotic Cell · doi:10.1128/ec.00251-08 · Cited by 47
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Takeshita, N., Diallinas, G., & Fischer, R. (2012) · Molecular Microbiology · doi:10.1111/j.1365-2958.2012.07996.x · Cited by 46
Self-citationIshitsuka, Y., Savage, N. S., Li, Y., Bergs, A., Grün, N., Kohler, D., Donnelly, R., Nienhaus, G. U., Fischer, R., & Takeshita, N. (2015) · Science Advances · doi:10.1126/sciadv.1500947 · Cited by 46
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Self-citation
Metadata
- Authors
- Takeshita, N., Higashitsuji, Y., Konzack, S., & Fischer, R.
- Affiliations
- Karlsruhe Institute of Technology (DE)
- Applied Microbiology, University of Karlsruhe, D-76187 Karlsruhe, Germany
- ORCID
- Takeshita, Norio
- Venue
- Molecular Biology of the Cell
- Published
- 2008-01
- Volume
- 19
- Issue
- 1
- Pages
- 339-351
- ISSN
- 1059-1524 (ISSN-L)
- 1939-4586
- PMC
- PMC2174190
- OpenAlex
- W2137246929
- Cited by
- 163
- References
- 58
- Citations by year
- 2026: 9 · 2025: 6 · 2024: 8 · 2023: 4 · 2022: 2 · 2021: 5 · 2020: 5 · 2019: 12 · 2018: 6 · 2017: 13 · 2016: 12 · 2015: 14 · 2014: 13 · 2013: 6 · 2012: 4
- FWCI
- 3.84
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Molecular Biology of the Cell (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Keywords
- Aspergillus nidulans, hyphal tip, polarized growth, tear, Spitzenkörper, vesicle trafficking, filipin, hyphal morphology
- MeSH terms
- Aspergillus nidulans, Cell Membrane, Filipin, Fungal Proteins, Microtubules, Phenotype, Protein Binding, Sterols, Biomarkers, Cell Polarity, Gene Deletion, Protein Transport, Hyphae
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