The purpose of this proposal is to study the function of a novel protein interacting with microtubules and microtubule-organizing centers (MTOCs). Microtubules are involved in vital cell processes including cell division and morphogenesis, and elucidation of the mechanism of microtubule functions and its regulation is crucial to an understanding of biological growth, differentiation and its pathologies. The key elements for regulation of microtubule functions are MAPs (Microtubule-associated proteins) and MTOCs which modulate properties of microtubules and direct organization of higher ordered structures which are essential for performance of microtubule functions. This proposal will focus on a molecule that has recently been identified by a monoclonal anti-phosphoprotein antibody, AX3, raised against MTOCs from the cellular slime mole, Dictyostelium discoideum. The AX3 antigen is a novel MAP associated with MTOCs in a wide range of organisms from fungi to human. The genes coding for the protein in different biological systems (Dictyostelium and HeLa cells) will be cloned and their nucleotide sequences will be compared. Phosphorylation properties of the antigen will be examined during the process of cell cycle and cell differentiation, and the effect of phosphorylation on its association with microtubules will be analyzed in The proteins' capacity to interact with other MTOC components will be examined by constructing affinity columns with fusion proteins produced using recombinant DNA technology. The gene corresponding to the AX3 antigen in Dictyostelium will be disrupted using the gene targeting method found to be successful in this organism, and the phenotype of transformed cells and changes in the microtubule organization and mitotic spindle formation will be analyzed by microscopy. The protein's role in HeLa cells will be evaluated by employing in vitro inhibition of microtubule assembly onto isolated centrosomes, and by microinjection of antibodies into living cells at different cell cycle stages. Intracellular concentration of the protein will be modulated either by introduction of antisense RNA, or microinjection of fusion proteins, or transfection of cells with DNAs expressing the AX3 antigen. Such studies on MAPs and their role in MTOC-directed regulation of microtubule organization enable us to analyze the molecular basis of the microtubule-dependent cellular processes, which will be important for understanding the mechanism of uncontrolled cell division and differentiation.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM041350-05
Application #
3299495
Study Section
Cellular Biology and Physiology Subcommittee 1 (CBY)
Project Start
1988-12-01
Project End
1995-11-30
Budget Start
1992-12-01
Budget End
1993-11-30
Support Year
5
Fiscal Year
1993
Total Cost
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Type
Schools of Medicine
DUNS #
168559177
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Ferhat, L; Kuriyama, R; Lyons, G E et al. (1998) Expression of the mitotic motor protein CHO1/MKLP1 in postmitotic neurons. Eur J Neurosci 10:1383-93
Yu, W; Sharp, D J; Kuriyama, R et al. (1997) Inhibition of a mitotic motor compromises the formation of dendrite-like processes from neuroblastoma cells. J Cell Biol 136:659-68
Lee, K S; Yuan, Y L; Kuriyama, R et al. (1995) Plk is an M-phase-specific protein kinase and interacts with a kinesin-like protein, CHO1/MKLP-1. Mol Cell Biol 15:7143-51
Vassilev, A; Kimble, M; Silflow, C D et al. (1995) Identification of intrinsic dimer and overexpressed monomeric forms of gamma-tubulin in Sf9 cells infected with baculovirus containing the Chlamydomonas gamma-tubulin sequence. J Cell Sci 108 ( Pt 3):1083-92
Kuriyama, R; Levin, A; Nelson, D et al. (1995) Monoclonal anti-dipeptide antibodies cross-react with detyrosinated and glutamylated forms of tubulins. Cell Motil Cytoskeleton 30:171-82
Kuriyama, R; Kofron, M; Essner, R et al. (1995) Characterization of a minus end-directed kinesin-like motor protein from cultured mammalian cells. J Cell Biol 129:1049-59
Kuriyama, R; Dragas-Granoic, S; Maekawa, T et al. (1994) Heterogeneity and microtubule interaction of the CHO1 antigen, a mitosis-specific kinesin-like protein. Analysis of subdomains expressed in insect sf9 cells. J Cell Sci 107 ( Pt 12):3485-99
Kuriyama, R; Maekawa, T (1992) Phosphorylation of a 225-kDa centrosomal component in mitotic CHO cells and sea urchin eggs. Exp Cell Res 202:345-54
Kimble, M; Kuriyama, R (1992) Functional components of microtubule-organizing centers. Int Rev Cytol 136:1-50
Kimble, M; Khodjakov, A L; Kuriyama, R (1992) Identification of ubiquitous high-molecular-mass, heat-stable microtubule-associated proteins (MAPs) that are related to the Drosophila 205-kDa MAP but are not related to the mammalian MAP-4. Proc Natl Acad Sci U S A 89:7693-7

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