The proposed research is directed towards understanding at a molecular level how chromosomes are moved to daughter cells during cell division by the mitotic spindle.
The specific aim of this grant is to determine how the polymerization of microtubules at their site of attachment to chromosomes (the kinetochore) is regulated, and how polymerization and depolymerization at the kinetochore contribute to chromosome movement. Kinetic and structural methods will be used to probe the difference between polymerizing and depolymerizing microtubule ends and how they spontaneously interconvert (dynamic instability). Models which postulate that growing microtubules are stabilized by a cap of GTP containing subunits will be tested by following GTP hydrolysis during polymerization, and examining the effects of non-hydrolyseable analogues on depolymerization rate. The modification of inherent microtubule dynamic behavior which occurs after their capture by kinetochores will be studied in vitro using immunofluorescent and real-time assays. These experiments will examine the role of ATP hydrolysis in microtubule polymerization at the kinetochore and test whether kinetochores can be pulled polewards by depolymerizing microtubules. Functional in vitro assays will be complemented by probing microtubule dynamics in living mitotic cells. A novel photoactivable fluorescent probe attached to tubulin will be used to assess the contribution of microtubule polymerization at the kinetochore to chromosome congression during prometaphase, and the extent to which anaphase movement occurs by depolymerization there. Biochemical methods will be used to bring the analysis of kinetochore function to a molecular level. Cross-linking to tubulin, microtubule affinity, ATP photoaffinity labeling, and subfractionation will be used to identify and characterize the molecules in the kinetochores of isolated mitotic chromosomes responsible for interaction with microtubules. Understanding microtubule dynamics at the kinetochore and its role in chromosome movement may lead to better methods for interfering with the cell-division of tumor cells and parasites, and to the construction of artificial chromosomes for genetic manipulation of food-animals and crops.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM039565-03
Application #
3296669
Study Section
Molecular Cytology Study Section (CTY)
Project Start
1988-02-01
Project End
1993-01-31
Budget Start
1990-02-01
Budget End
1991-01-31
Support Year
3
Fiscal Year
1990
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
Schools of Medicine
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Nguyen, P A; Field, C M; Mitchison, T J (2018) Prc1E and Kif4A control microtubule organization within and between large Xenopus egg asters. Mol Biol Cell 29:304-316
Pineda, Javier J; Miller, Miles A; Song, Yuyu et al. (2018) Site occupancy calibration of taxane pharmacology in live cells and tissues. Proc Natl Acad Sci U S A 115:E11406-E11414
Field, Christine M; Mitchison, Timothy J (2018) Assembly of Spindles and Asters in Xenopus Egg Extracts. Cold Spring Harb Protoc 2018:pdb.prot099796
Liu, Ling; Su, Xiaoyang; Quinn 3rd, William J et al. (2018) Quantitative Analysis of NAD Synthesis-Breakdown Fluxes. Cell Metab 27:1067-1080.e5
Presler, Marc; Van Itallie, Elizabeth; Klein, Allon M et al. (2017) Proteomics of phosphorylation and protein dynamics during fertilization and meiotic exit in the Xenopus egg. Proc Natl Acad Sci U S A 114:E10838-E10847
Costigliola, Nancy; Ding, Liya; Burckhardt, Christoph J et al. (2017) Vimentin fibers orient traction stress. Proc Natl Acad Sci U S A 114:5195-5200
Hanley, Mariah L; Yoo, Tae Yeon; Sonnett, Matthew et al. (2017) Chromosomal passenger complex hydrodynamics suggests chaperoning of the inactive state by nucleoplasmin/nucleophosmin. Mol Biol Cell 28:1444-1456
Mitchison, Timothy J; Field, Christine M (2017) Spindle-to-Cortex Communication in Cleaving Frog Eggs. Cold Spring Harb Symp Quant Biol 82:165-171
Guild, Joshua; Ginzberg, Miriam B; Hueschen, Christina L et al. (2017) Increased lateral microtubule contact at the cell cortex is sufficient to drive mammalian spindle elongation. Mol Biol Cell 28:1975-1983
Boke, Elvan; Mitchison, Timothy J (2017) The balbiani body and the concept of physiological amyloids. Cell Cycle 16:153-154

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