Mitotic chromosome segregation is accomplished by the spindle, a motile microtubule-based structure. In the simple eukaryote S. cerevisiae, all of the microtubule-based motor proteins of the kinesin and dynein families are now known (total of six and one, respectively). Most act within the spindle, but the roles performed by each are not completely understood. A major goal of the proposed experiments is to determine these roles and the nature of the complex interactions exhibited by these motors. We are focusing upon two uncharacterized kinesin-related motors, Rrc805p and Kip2p, that we have linked to the essential process of mitotic spindle positioning (or """"""""nuclear migration""""""""). Surprisingly, these two motors and the dynein nuclear migration motor can all be eliminated without causing lethality. This indicates a previously unappreciated nuclear migration role for at least one of the four remaining kinesin-related motors (or the presence of novel microtubule-based motors - see below). We have also revealed a deleterious action of the Kip2p motor in the absence of dynein and Rrc8O5p. The causes of these related effects will be revealed by the construction of multiple motor mutant strains and observing the in vivo behavior of spindles and chromosomes. We will also perform a series of experiments designed to determine the molecular mechanism of action of the most important spindle assembly and pole-separating motor, Cin8p. This motor belongs to the BimC family of kinesin-related proteins that is conserved throughout the eukaryotes. The structure and function of wild- type and mutant Cin8p motor complexes will be examined by in vivo and in vitro assays. We have determined that the tail domain of Cin8p is required for multimerization, proper localization and normal regulation. These properties will be explored further. We will also describe the mechanisms of cell cycle regulation that act upon Cin8p. Finally, we will investigate the mitotic role performed by MONl, the largest gene in yeast, encoding a protein with features similar to molecular motors.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM040714-13
Application #
6180099
Study Section
Cellular Biology and Physiology Subcommittee 1 (CBY)
Program Officer
Deatherage, James F
Project Start
1988-07-01
Project End
2001-07-31
Budget Start
2000-08-01
Budget End
2001-07-31
Support Year
13
Fiscal Year
2000
Total Cost
$261,830
Indirect Cost
Name
Johns Hopkins University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Hildebrandt, Emily R; Gheber, Larisa; Kingsbury, Tami et al. (2006) Homotetrameric form of Cin8p, a Saccharomyces cerevisiae kinesin-5 motor, is essential for its in vivo function. J Biol Chem 281:26004-13
Hildebrandt, E R; Hoyt, M A (2001) Cell cycle-dependent degradation of the Saccharomyces cerevisiae spindle motor Cin8p requires APC(Cdh1) and a bipartite destruction sequence. Mol Biol Cell 12:3402-16
Hildebrandt, E R; Hoyt, M A (2000) Mitotic motors in Saccharomyces cerevisiae. Biochim Biophys Acta 1496:99-116
Gheber, L; Kuo, S C; Hoyt, M A (1999) Motile properties of the kinesin-related Cin8p spindle motor extracted from Saccharomyces cerevisiae cells. J Biol Chem 274:9564-72
Cottingham, F R; Gheber, L; Miller, D L et al. (1999) Novel roles for saccharomyces cerevisiae mitotic spindle motors. J Cell Biol 147:335-50
Saunders, W; Lengyel, V; Hoyt, M A (1997) Mitotic spindle function in Saccharomyces cerevisiae requires a balance between different types of kinesin-related motors. Mol Biol Cell 8:1025-33
Geiser, J R; Schott, E J; Kingsbury, T J et al. (1997) Saccharomyces cerevisiae genes required in the absence of the CIN8-encoded spindle motor act in functionally diverse mitotic pathways. Mol Biol Cell 8:1035-50
Cottingham, F R; Hoyt, M A (1997) Mitotic spindle positioning in Saccharomyces cerevisiae is accomplished by antagonistically acting microtubule motor proteins. J Cell Biol 138:1041-53
Hoyt, M A; Macke, J P; Roberts, B T et al. (1997) Saccharomyces cerevisiae PAC2 functions with CIN1, 2 and 4 in a pathway leading to normal microtubule stability. Genetics 146:849-57
Hoyt, M A; He, L; Totis, L et al. (1993) Loss of function of Saccharomyces cerevisiae kinesin-related CIN8 and KIP1 is suppressed by KAR3 motor domain mutations. Genetics 135:35-44

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