The Saccharomyces cerevisiae spindle pole body is a dynamic structure

Molecular Biology of the Cell

Volumn 14, Issue 8, 2003, Pages 3494-3505

  Yoder, Tennessee J ^a   Pearson, Chad G ^b   Bloom, Kerry ^b   Davis, Trisha N ^a  

^a UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF NORTH CAROLINA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MICROTUBULE PROTEIN; PROTEIN SPC110P; UNCLASSIFIED DRUG;

ARTICLE; CELL CYCLE; CELL CYCLE G1 PHASE; CELL CYCLE G2 PHASE; CELL CYCLE S PHASE; FLUORESCENCE; FUNGUS GROWTH; MITOSIS INHIBITION; NONHUMAN; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; SACCHAROMYCES CEREVISIAE; SPINDLE POLE BODY;

CELL CYCLE; G1 PHASE; G2 PHASE; MITOSIS; MITOTIC SPINDLE APPARATUS; NUCLEAR PROTEINS; SACCHAROMYCES CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEINS;

FUNGI; SACCHAROMYCES; SACCHAROMYCES CEREVISIAE;

EID: 0042970575     PISSN: 10591524     EISSN: None     Source Type: Journal    
DOI: 10.1091/mbc.E02-10-0655     Document Type: Article

References (52)

1. Adams, I.R., and Kilmartin, J.V. (1999). Localization of core spindle pole body (SPB) components during SPB duplication in Saccharomyces cerevisiae. J. Cell Biol. 145, 809-823.
2. Bardin, A.J., Visintin, R., and Amon, A. (2000). A mechanism for coupling exit from mitosis to partitioning of the nucleus. Cell 102, 21-31.
3. Bevis, B.J., and Glick, B.S. (2002). Rapidly maturing variants of the Discosoma red fluorescent protein (DsRed). Nat. Biotechnol. 20, 83-87.
4. Bullitt, E., Rout, M.P., Kilmartin, J.V., and Akey, C.W. (1997). The yeast spindle pole body is assembled around a central crystal of Spc42p. Cell 89, 1077-1086.
5. Byers, B., and Goetsch, L. (1974). Duplication of spindle plaques and integration of the yeast cell cycle. Cold Spring Harb. Symp. Quant. Biol. 38, 123-131.
6. Byers, B., and Goetsch, L. (1975). Behavior of spindles and spindle plaques in the cell cycle and conjugation of Saccharomyces cerevisiae. J. Bacteriol. 124, 511-523.
7. Cenamor, R., Jimenez, J., Cid, V.J., Nombela, C., and Sanchez, M. (1999). The budding yeast Cdc15 localizes to the spindle pole body in a cell-cycle-dependent manner. Mol. Cell. Biol. Res. Commun 2, 178-184.
8. Davis, T.N. (1992). A temperature-sensitive calmodulin mutant loses viability during mitosis. J. Cell Biol. 118, 607-617.
9. Ding, R., West, R.R., Morphew, D.M., Oakley, B.R., and McIntosh, J.R. (1997). The spindle pole body of Schizosaccharomyces pombe enters and leaves the nuclear envelope as the cell cycle proceeds. Mol. Biol. Cell 8, 1461-1479.
10. Donaldson, A.D., and Kilmartin, J.V. (1996). Spc42p: a phosphorylated component of the S. cerevisiae spindle pole body (SPD) with an essential function during SPB duplication. J. Cell Biol. 132, 887-901.
11. Elliott, S., Knop, M., Schlenstedt, G., and Schiebel, E. (1999). Spc29p is a component of the Spc110p subcomplex and is essential for spindle pole body duplication. Proc. Natl. Acad. Sci. USA 96, 6205-6210.
12. Friedman, D.B., Sundberg, H.A., Huang, E.Y., and Davis, T.N. (1996). The 110-kD spindle pole body component of Saccharomyces cerevisiae is a phosphoprotein that is modified in a cell cycle-dependent manner. J. Cell Biol. 132, 903-914.
13. Garvik, B., Carson, M., and Hartwell, L. (1995). Single-stranded DNA arising at telomeres in cdc13 mutants may constitute a specific signal for the RAD9 checkpoint. Mol. Cell. Biol. 15, 6128-6138.
14. Geiser, J.R., van-Tuinen, D., Brockerhoff, S.E., Neff, M.M., and Davis, T.N. (1991). Can calmodulin function without binding calcium? Cell 65, 949-959.
15. Hardwick, K.G., Weiss, E., Luca, F.C., Winey, M., and Murray, A.W. (1996). Activation of the budding yeast spindle assembly checkpoint without mitotic spindle disruption. Science 273, 953-956.
16. Heath, I.B. (1980). Behavior of kinetochores during mitosis in the fungus Saprolegnia ferax. J. Cell Biol. 84, 531-546.
17. Howell, B.J., Hoffman, D.B., Fang, G., Murray, A.W., and Salmon, E.D. (2000). Visualization of Mad2 dynamics at kinetochores, along spindle fibers, and at spindle poles in living cells. J. Cell Biol. 150, 1233-1250.
18. Irniger, S., Piatti, S., Michaelis, C., and Nasmyth, K. (1995). Genes involved in sister chromatid separation are needed for B-type cyclin proteolysis in budding yeast. Cell 81, 269-278.
19. Janke, C., Ortiz, J., Tanaka, T.U., Lechner, J., and Schiebel, E. (2002). Four new subunits of the Daml-Duol complex reveal novel functions in sister kinetochore biorientation. EMBO J. 21, 181-193.
20. Jaspersen, S.L., Charles, J.F., Tinker-Kulberg, R.L., and Morgan, D.O. (1998). A late mitotic regulatory network controlling cyclin destruction in Saccharomyces cerevisiae. Mol. Biol. Cell 9, 2803-2817.
21. Kallio, M.J., Beardmore, V.A., Weinstein, J., and Gorbsky, G.J. (2002). Rapid microtubule-independent dynamics of Cdc20 at kinetochores and centrosomes in mammalian cells. J. Cell Biol. 158, 841-847.
22. Khodjakov, A., and Rieder, C.L. (1999). The sudden recruitment of gamma-tubulin to the centrosome at the onset of mitosis and its dynamic exchange throughout the cell cycle, do not require microtubules. J. Cell Biol. 146, 585-596.
23. Kilmartin, J.V., Dyos, S.L., Kershaw, D., and Finch, J.T. (1993). A spacer protein in the Saccharomyces cerevisiae spindle poly body whose transcript is cell cycle-regulated. J. Cell Biol. 123, 1175-1184.
24. King, R.W., Peters, J.M., Tugendreich, S., Rolfe, M., Hieter, P., and Kirschner, M.W. (1995). A 20S complex containing CDC27 and CDC16 catalyzes the mitosis-specific conjugation of ubiquitin to cyclin B. Cell 81, 279-288.
25. Kochanski, R.S., and Borisy, G.G. (1990). Mode of centriole duplication and distribution. J. Cell Biol. 110, 1599-1605.
26. Lew, D.J., Weinert, T., and Pringle, J.R. (1997). Cell cycle control in Saccharomyces cerevisiae. In: The Molecular and Cellular Biology of the Yeast Saccharomyces, vol. 3, ed. J.R. Pringle, J.R. Broach, and E.W. Jones, Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press, 607-696.
27. Maddox, P.S., Bloom, K.S., and Salmon, E.D. (2000). The polarity and dynamics of microtubule assembly in the budding yeast Saccharomyces cerevisiae. Nat. Cell Biol. 2, 36-41.
28. Marschall, L.G., Jeng, R.L., Mulholland, J., and Stearns, T. (1996). Analysis of Tub4p, a yeast gamma-tubulin-like protein: implications for microtubule-organizing center function. J. Cell Biol. 134, 443-454.
29. Mathias, N., Johnson, S.L., Winey, M., Adams, A.E., Goetsch, L., Pringle, J.R., Byers, B., and Goebl, M.G. (1996). Cdc53p acts in concert with Cdc4p and Cdc34p to control the G1-to-S-phase transition and identifies a conserved family of proteins. Mol. Cell. Biol. 16, 6634-6643.
30. Mayer, V.W., and Aguilera, A. (1990). High levels of chromosome instability in polyploids of Saccharomyces cerevisiae. Mutat. Res. 231, 177-186.
31. Menssen, R., Neutzner, A., and Seufert, W. (2001). Asymmetric spindle pole localization of yeast Cdc15 kinase links mitotic exit and cytokinesis. Curr. Biol. 11, 345-350.
32. Neff, M.W., and Burke, D.J. (1991). Random segregation of chromatids at mitosis in Saccharomyces cerevisiae. Genetics 127, 463-473.
33. O'Toole, E.T., Mastronarde, D.N., Giddings, T.H., Jr., Winey, M., Burke, D.J., and McIntosh, J.R. (1997). Three-dimensional analysis and ultrastructural design of mitotic spindles from the cdc20 mutant of Saccharomyces cerevisiae. Mol. Biol. Cell 8, 1-11.
34. O'Toole, E.T., Winey, M., and McIntosh, J.R. (1999). High-voltage electron tomography of spindle pole bodies and early mitotic spindles in the yeast Saccharomyces cerevisiae. Mol. Biol. Cell 10, 2017-2031.
35. Pereira, G., Hofken, T., Grindlay, J., Manson, C., and Schiebel, E. (2000). The Bub2p spindle checkpoint links nuclear migration with mitotic exit. Mol. Cell 6, 1-10.
36. Pereira, G., Tanaka, T.U., Nasmyth, K., and Schiebel, E. (2001). Modes of spindle pole body inheritance and segregation of the Bfa1p-Bub2p checkpoint protein complex. EMBO J. 20, 6359-6370.
37. Piatti, S., Lengauer, C., and Nasmyth, K. (1995). Cdc6 is an unstable protein whose de novo synthesis in G1 is important for the onset of S phase and for preventing a 'reductional' anaphase in the budding yeast Saccharomyces cerevisiae. EMBO J. 14, 3788-3799.
38. Schutz, A.R., and Winey, M. (1998). New alleles of the yeast MPS1 gene reveal multiple requirements in spindle pole body duplication. Mol. Biol. Cell 9, 759-774.
39. Schuyler, S.C., Liu, J.Y., and Pellman, D. (2003). The molecular function of Aselp: evidence for a MAP-dependent midzone-specific spindle matrix. J. Cell Biol. 160, 517-528.
40. Sherman, F., Fink, G.R., and Hicks, J.B. (1986). Methods in Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press Yeast Genetics, Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press.
41. Sikorski, R.S., and Hieter, P. (1989). A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae. Genetics 122, 19-27.
42. Stern, B.M., and Murray, A.W. (2001). Lack of tension at kinetochores activates the spindle checkpoint in budding yeast. Curr. Biol. 11, 1462-1467.
43. Stricker, J., Maddox, P., Salmon, E.D., and Erickson, H.P. (2002). Rapid assembly dynamics of the Escherichia coli FtsZ-ring demonstrated by fluorescence recovery after photobleaching. Proc. Natl. Acad. Sci. USA 99, 3171-3175.
44. Sundberg, H.A., and Davis, T.N. (1997). A mutational analysis identifies three functional regions of the spindle pole component Spc110p in Saccharomyces cerevisiae. Mol. Biol. Cell 8, 2575-2590.
45. Sundberg, H.A., Goetsch, L., Byers, B., and Davis, T.N. (1996). Role of calmodulin and Spc110p interaction in the proper assembly of spindle pole body components. J. Cell Biol. 133, 111-124.
46. Swaminathan, R., Hoang, C.P., and Verkman, A.S. (1997). Photo-bleaching recovery and anisotropy decay of green fluorescent protein GFP-S65T in solution and cells: cytoplasmic viscosity probed by green fluorescent protein translational and rotational diffusion. Biophys. J. 72, 1900-1907.
47. Tanaka, T.U., Rachidi, N., Janke, C., Pereira, G., Galova, M., Schiebel, E., Stark, M.J., and Nasmyth, K. (2002). Evidence that the Ipl-Sli15 (Aurora kinase-INCENP) complex promotes chromosome bi-orientation by altering kinetochore-spindle pole connections. Cell 108, 317-329.
48. Wach, A., Brachat, A., Alberti-Segui, C., Rebischung, C., and Philippsen, P. (1997). Heterologous HIS3 marker and GFP reporter modules for PCR-targeting in Saccharomyces cerevisiae. Yeast 13, 1065-1075.
49. Wasch, R., and Cross, F.R. (2002). APC-dependent proteolysis of the mitotic cyclin Clb2 is essential for mitotic exit. Nature 418, 556-562.
50. Winey, M., Goetsch, L., Baum, P., and Byers, B. (1991). MPS1 and MPS 2, novel yeast genes defining distinct steps of spindle pole body duplication. J. Cell Biol. 114, 745-754.
51. Xu, S., Huang, H.K., Kaiser, P., Latterich, M., and Hunter, T. (2000). Phosphorylation and spindle pole body localization of the Cdc15p mitotic regulatory protein kinase in budding yeast. Curr. Biol. 10, 329-332.
52. Zachariae, W., and Nasmyth, K. (1996). TPR proteins required for anaphase progression mediate ubiquitination of mitotic B-type cyclins in yeast. Mol. Biol. Cell 7, 791-801.