The long-range goal of this research is to understand the purpose and mechanism of a cytoskeletal differentiation, that is, modifications in the cytoskeleton which alter its role in cellular events. In particular, a reversible post-translational modification of a tubulin involves the addition or removal of a tyrosine residue at the C terminus. Previous research in the laboratory has determined that tyrosinated and nontyrosinated tubulin are contained in different populations of macrotubules in cultured cells.
The aims of this project are three-fold: (1) to determine whether asymmetry of distribution of nontyrosinated (Glu) and tyrosinated (Tyr) tubulins in microtubules is of widespread occurrence; (2) to ascertain whether or not the segregation of the Glu and Tyr tubulins into separate microtubules appears to be involved in mitosis or cell transformation; and (3) to determine the mechanism by which these two post-translationally modified tubulins become differentially distributed in vivo. Several types of cultured cells will be examined using peptide antibodies specific for Tyr and for Glu tubulin. Cells engaged in mitosis will be examined with light and electron microscopic immunolocalization in order to determine which population of mitotic microtubules contain which species of alpha-tubulin. Transformation by SV40 virus in two cell lines will be used as an example of cytoskeletal abnormalities induced by transformation. In each case in which asymmetry of Tyr and Glu tubulin is observed, the location and any putative functions of microtubules containing each will be noted. To learn about the significance and the mechanism of obtaining the observed differential distribution of Tyr and Glu tubulin, microtubules will be depolymerized in vivo and in lysed cell models. Repolymerization under several conditions will result in differential or equivalent distributions of Glu and Tyr tubulin. Several possible mechanisms for the segregation of Glu and Tyr tubulins into separate microtubules can thus be tested. Since the abnormal function of microtubules is an integral part of cancer and other diseases, attempts to discover the control of their localization and function in cell division, differentiation, and transformation is of obvious importance. (L)

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
1R01CA039755-01
Application #
3179154
Study Section
Cellular Biology and Physiology Subcommittee 1 (CBY)
Project Start
1985-04-01
Project End
1988-03-31
Budget Start
1985-04-01
Budget End
1986-03-31
Support Year
1
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Type
Schools of Arts and Sciences
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Chapin, S J; Bulinski, J C (1994) Cellular microtubules heterogeneous in their content of microtubule-associated protein 4 (MAP4). Cell Motil Cytoskeleton 27:133-49
Bulinski, J C; Bossler, A (1994) Purification and characterization of ensconsin, a novel microtubule stabilizing protein. J Cell Sci 107 ( Pt 10):2839-49
Webster, D R; Modesti, N M; Bulinski, J C (1992) Regulation of cytoplasmic tubulin carboxypeptidase activity during neural and muscle differentiation: characterization using a microtubule-based assay. Biochemistry 31:5849-56
Bulinski, J C; Gundersen, G G (1991) Stabilization of post-translational modification of microtubules during cellular morphogenesis. Bioessays 13:285-93
Gundersen, G G; Bulinski, J C (1988) Selective stabilization of microtubules oriented toward the direction of cell migration. Proc Natl Acad Sci U S A 85:5946-50
Khawaja, S; Gundersen, G G; Bulinski, J C (1988) Enhanced stability of microtubules enriched in detyrosinated tubulin is not a direct function of detyrosination level. J Cell Biol 106:141-9
Bulinski, J C; Richards, J E; Piperno, G (1988) Posttranslational modifications of alpha tubulin: detyrosination and acetylation differentiate populations of interphase microtubules in cultured cells. J Cell Biol 106:1213-20
Webster, D R; Gundersen, G G; Bulinski, J C et al. (1987) Assembly and turnover of detyrosinated tubulin in vivo. J Cell Biol 105:265-76
Webster, D R; Gundersen, G G; Bulinski, J C et al. (1987) Differential turnover of tyrosinated and detyrosinated microtubules. Proc Natl Acad Sci U S A 84:9040-4
Gundersen, G G; Khawaja, S; Bulinski, J C (1987) Postpolymerization detyrosination of alpha-tubulin: a mechanism for subcellular differentiation of microtubules. J Cell Biol 105:251-64

Showing the most recent 10 out of 13 publications