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Ryoko Kuriyama, Ph.D.

Professor


Mailing Address:
University of Minnesota
Department of Genetics, Cell Biology, and Development
6-160 Jackson
321 Church St. SE
Minneapolis, MN 55455
USA


Education:
Ph.D., 1976, University of Tokyo, Tokyo, Japan;

Office:
6-134 MCB
P: 612-624-0471
F: 612-624-8118

Email:
kuriy001@umn.edu
Lab:

P: 612-626-4089

Areas of Research Strength:

Molecular cell biology of microtubule-organizing centers,
mitosis, cell growth, and cell cycle regulation in eukaryotic cells.


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Research Techniques:

Mammalian cell culture and synchronization
Centrosome biology
Molecular biology of mitotic spindles and spindle poles
Protein biochemistry

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Research Interests:

The research in Kuriyama's focuses on the cell cycle and cell growth
control in mammalian cells, and current efforts are oriented towards
understanding the molecular mechanism and regulation of mitosis and
cytoplasmic division using multidisciplinary experimental approaches.
Molecular components of the mitotic spindle and spindle poles were
analyzed by establishing the isolation procedure of highly purified
mitotic spindles from synchronized cultured cells, followed by generation
of monoclonal antibodies and screening of expression as well as two
hybrid libraries. Among dozens of molecules identified, the lab currently
focus on centrosomal components located at each spindle pole, and
a microtubule motor protein essential for completion of cytokinesis
via its interaction with small G-proteins and actin filaments at the
spindle midzone. By introducing small interfering RNA and rescue
constructs, the lab evaluates their roles in the assembly and function
of centrosomes, and coordination of cell cycle events during cell
division cycle.

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Selected Publications:

Kuriyama, R., C. Besse, M. Geze, C.K. Omoto, and J. Schrevel. 2005. Dynamic organization of microtubules and microtubule-organizing centers during the sexual phase of a parasitic protozoan, Lecudina tuzetae (Gregarine, Apicomplexa). Cell Motility Cytoskel. 62:195-209 (journal cover page)

Kuriyama, R., and J. Matuliene. 2005. Kinesin-like motor protein MKLP1/CHO1 in cytokinesis. In: Signal Transduction of Cell Division. T. Miki, ed., Research Signpost, Kerala, India.

Kuriyama, R. 2005. Mitotic Spindles. In: Encyclopedic Reference of Genomics and Proteomic in Molecular Medicine. Molecular Principles. Springer Verlag, Heidelberg.

Nelsen, C.J., R. Kuriyama, B. Hirsch, V.C. Negron, W.L. Lingle, M.M. Goggin, M.W. Stanley, and J.H. Albrecht. 2005. Short-term cyclin D1 overexpression induces centrosome amplification, mitotic abnormalities, and aneuploidy. J. Biol. Chem.280:768-776.

Matuliene, J., and R. Kuriyama. 2004. Role of CHO1 in mammalian cytokinesis: RNAi and genetic rescue analysis. Mol. Biol. Cell 15:3083-3094.

Uetake, Y., Y. Terada, J. Matuliene, and R. Kuriyama. 2004. Interaction of Cep135 with a p50 dynactin subunit in mammalian centrosomes. Cell Motility Cytoskel. 58:53-66.

Terada, Y., Y. Uetake, and R. Kuriyama. 2003. Interaction of Aurora-A and centrosomin at the microtubule-nuleating sites in Drosophila and mammalian cells. J. Cell Biol. 162:757-763.

Kuriyama, R., C. Gustus, Y. Terada, Y. Uetake, and J. Matuliene. 2002. CHO1, a mammalian kinesin-like protein, interacts with F-actin and is involved in the terminal phase of cytokinesis. J. Cell Biol. 156:783-790.

Matuliene, J., and R. Kuriyama. 2002. Kinesin-like motor protein CHO1 is required for the formation of midbody matrix and the completion of cytokinesis in mammalian cells. Mol. Biol. Cell 13:1832-1845.

Ohta, T., R. Essner, J.-H. Ryu, R.E. Palazzo, and R. Kuriyama. 2002. Characterization of Cep135, a novel centrosomal protein involved in microtubule organization in mammalian cells. J. Cell Biol. 156:87-99.


To view these and other publications visit http://www.ncbi.nlm.nih.gov/PubMed
search menu should say PubMed
type Kuriyama R in the avaliable line

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