- 1) Solomon, F., Analyses of the cytoskeleton in Saccharomyces cerevisiae. Annu. Rev. Cell Biol., 7, 633–662 (1991).
- 2) Botstein, D., Amberg, D., Mulholland, J., Huffaker, T., Adams, A., Drubin, D., and Stearns, T., The yeast cytoskeleton, 1. In “The Molecular and Cellular Biology of the Yeast Saccharomyces cerevisiae,” eds. Pringle, J. R., Broach, J. R., and Jones, E. W., Cold Spring Harbor Laboratory Press, New York, pp. 1–90 (1997).
- 3) Shitamukai, A., Mizunuma, M., Hirata, D., Takahashi, H., and Miyakawa, T., A positive screening for drugs that specifically inhibit the Ca2+-signaling activity on the basis of the growth promoting effect on a yeast mutant with a peculiar phenotype. Biosci. Biotechnol. Biochem., 64, 1942–1946 (2000).
- 4) Miyakawa, T., and Mizunuma, M., Physiological roles of calcineurin in Saccharomyces cerevisiae with special emphasis on its roles in G2/M cell-cycle regulation. Biosci. Biotechnol. Biochem., 71, 633–645 (2007).
- 5) Chanklan, R., Aihara, E., Koga, S., Takahashi, H., Mizunuma, M., and Miyakawa, T., Inhibition of Ca2+-signal-dependent growth regulation by radicicol in budding yeast. Biosci. Biotechnol. Biochem., 72, 132–138 (2008).
- 6) Koizumi, F., Fukumitsu, N., Zhao, J., Chanklan, R., Miyakawa, T., Kawahara, S., Iwamoto, S., Suzuki, M., Kakita, S., Rahayu, E. S., Hosokawa, S., Tatsuta, K., and Ichimura, M., YCM1008A, a novel Ca2+-signaling inhibitor, produced by Fusarium sp. YCM1008. J. Antibiotics, 60, 455–458 (2007).
- 7) Miyamoto, Y., Machida, K., Mizunuma, M., Emoto, Y., Sato, N., Miyahara, K., Hirata, D., Usui, T., Takahashi, H., Osada, H., and Miyakawa, T., Identification of Saccharomyces cerevisiae isoleucyl-tRNA synthetase as target of G1-specific inhibitor of reveromycin A. J. Biol. Chem., 277, 28810–28814 (2002).
- 8) Kongkathip, N., Hasitapan, K., Pradidphol, N., Kirtikara, K., Jongkon, N., and Kongkathip, B., Synthesis of novel 2-(2′-cyclopentyo)- and 2-(2′-cyclohexyl) substituted 1-naphthol derivatives with anticyclooxygenase activity. Curr. Med. Chem., 13, 3663–3674 (2006).
- 9) Mizunuma, M., Hirata, D., Miyaoka, R., and Miyakawa, T., GSK-3 kinase Mck1 and calcineurin coordinately mediate Hsl1 down-regulation by Ca2+ in budding yeast. EMBO J., 20, 1074–1085 (2001).
- 10) Kobayashi, Y., Mizunuma, M., Osada, H., and Miyakawa, T., Identification of Saccharomyces cerevisiae ribosomal protein L3 as a target of curvularol, a G1-specific inhibitor of mammalian cells. Biosci. Biotechnol. Biochem., 70, 2451–2459 (2006).
- 11) Straight, A. F., Marshall, W. F., Sedat, J. W., and Murray, A. W., Mitosis in living budding yeast: anaphase A but no metaphase plate. Science, 277, 574–578 (1997).
- 12) Mizunuma, M., Hirata, D., Miyahara, K., Tsuchiya, E., and Miyakawa, T., Role of calcineurin and Mpk1 in regulating the onset of mitosis in budding yeast. Nature, 392, 303–306 (1998).
- 13) Jacobs, C. W., Adams, A. E. M., Szaniszle, P. J., and Pringle, J. R., Functions of microtubules in the Saccharomyces cerevisiae cell cycle. J. Cell Biol., 107, 1409–1426 (1988).
- 14) Schatz, P. J., Solomon, F., and Botstein, D., Genetically essential and nonessential alpha-tubulin gene specify functionally interchangeable proteins. Mol. Cell. Biol., 6, 3722–3733 (1986).
- 15) Usui, T., Watanabe, H., Nakayama, H., Tada, Y., Kanoh, N., Kondoh, M., Asao, T., Takio, K., Watanabe, H., Nishikawa, K., Kitahara, T., and Osada, H., The anticancer natural product pironetin selectively targets Lys352 of α-tubulin. Chem. Biol., 11, 799–806 (2004).
- 16) Nogales, E., Wolf, S. G., and Downing, K. H., Structure of αβ tubulin dimer by electron crystallography. Nature, 391, 199–202 (1998).
- 17) Anders, K. R., and Botstein, D., Dominant-lethal α-tubulin mutants defective in microtubule depolymerization in yeast. Mol. Biol. Cell, 12, 3973–3986 (2001).
- 18) Anthony, R. G., Waldin, T. R., Ray, J. A., Bright, S. W. J., and Hussey, P. J., Herbicide resistance caused by spontaneous mutation of the cytoskeletal protein tubulin. Nature, 393, 260–263 (1998).
Full access
Identification of Saccharomyces cerevisiae Tub1 α-Tubulin as a Potential Target for NKH-7, a Cytotoxic 1-Naphthol Derivative Compound
Reprints and Corporate Permissions
Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?
To request a reprint or corporate permissions for this article, please click on the relevant link below:
Academic Permissions
Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?
Obtain permissions instantly via Rightslink by clicking on the button below:
If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.
Related research
People also read lists articles that other readers of this article have read.
Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.
Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.