The mechanisms by which muscle cells construct thick filaments of precise dimensions from myosin and associated proteins under biological regulation are the central focus of this proposal. The structure and assembly of thick filaments of the nematode, Caenorhabditis elegans are studied because of the continuing usefulness of mutants in uncovering new information and the increasing store of genetic, molecular and cellular information about this organism and its muscles.
The first aim i s to complete current work on the macromolecular composition of the thick filaments. Resolution of the components of the core structures within the filament backbones is a major goal. The localization of these and other macromolecular components in addition to the established two myosins and paramyosin by the development and use of specific antibodies will complete this aim.
The second aim will pursue partial reconstitution of nematode thick filaments from previously dissociated myosin, paramyosin and core structures. The establishment of conditions for depolymerization and repolymerization of isolated core structures will complete this aim.
The third aim concerns the newly discovered assemblages of multiple thick filament-related structures that are enriched in specific nematode mutants. Do the distributions of the two myosins and paramyosin change with time? Can isolated assemblages produce thick filaments in vitro? What are the biochemical requirements in terms of specific proteins and cofactors for either dynamical change? The fourth aim is an analysis of additional mutants by the kinetic results of the third aim so as to potentially order genetically specified functions with respect to the sequence of events in thick filament assembly. Further, the effects upon assembly of genetically altering the amounts of specific filament components synthesized will be monitored. The understanding of the mechanisms for assembly of thick filaments in C.elegans is directly relevant to development, physiological and pathological problems in human skeletal muscle and provides useful models for the roles of gene products in the morphogenesis of differentiated tissues that are important in many inherited human diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM033223-06
Application #
3282650
Study Section
Molecular Cytology Study Section (CTY)
Project Start
1984-04-01
Project End
1991-07-31
Budget Start
1990-02-01
Budget End
1991-07-31
Support Year
6
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Baylor College of Medicine
Department
Type
Schools of Medicine
DUNS #
074615394
City
Houston
State
TX
Country
United States
Zip Code
77030
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Epstein, H F; Lu, G Y; Deitiker, P R et al. (1995) Preliminary three-dimensional model for nematode thick filament core. J Struct Biol 115:163-74
Liu, F; Thatcher, J D; Barral, J M et al. (1995) Bifunctional glyoxylate cycle protein of Caenorhabditis elegans: a developmentally regulated protein of intestine and muscle. Dev Biol 169:399-414
Epstein, H F; Bernstein, S I (1992) Genetic approaches to understanding muscle development. Dev Biol 154:231-44
Epstein, H F; Fischman, D A (1991) Molecular analysis of protein assembly in muscle development. Science 251:1039-44