The mechanisms by which muscle cells construct thick filaments from myosin and associated proteins are the central focus of this proposal. Thick filament structure and assembly are studied in the nematode, Caenorhabditis elegans because of the utility of mutants in discovering new relationships and proteins and the ever-increasing store of genetic, molecular, and cellular information on this organism and its muscles.
The first aim i s to molecularly characterize associated thick filament proteins by peptide sequencing, cloning, and DNA sequencing. Are any proteins other than myosin and paramyosin chains associated with thick filaments? What is their molecular structure? Where are they located? Do any localize to the core substructure? The second aim is to study paramyosin-core substructures as potential templates in thick filament assembly. Do core substructures act as molecular templates for the assembly of paramyosin and myosin? Do the reassembled filaments show native length? Are associated proteins involved in this regulated assembly? The third aim is to purify and characterize multi-filament assemblages. Do these assemblages have associated proteins not found in thick filaments? Are any thick filament proteins missing in assemblages? Are any assemblage-specific proteins structurally related to known molecular chaperons for assembly? The fourth aim concerns the dynamics of the assemblages with respect to thick filament assembly. Are assemblages active in thick filament assembly as intermediates or catalysts? Are the assemblages side products that accumulate when assembly is blocked or slowed? Do the assemblages represent complexes of disassembling thick filaments? Understanding the assembly of thick filaments in C. elegans relates directly to developmental, physiological , and pathological problems in human skeletal muscle and provides useful models for the roles of gene products in normal differentiation and morphogenesis and of altered proteins in inherited human diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM033223-10
Application #
2176923
Study Section
Molecular Cytology Study Section (CTY)
Project Start
1984-04-01
Project End
1996-07-31
Budget Start
1994-08-01
Budget End
1996-07-31
Support Year
10
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Baylor College of Medicine
Department
Neurology
Type
Schools of Medicine
DUNS #
074615394
City
Houston
State
TX
Country
United States
Zip Code
77030
Liu, F; Barral, J M; Bauer, C C et al. (1997) Assemblases and coupling proteins in thick filament assembly. Cell Struct Funct 22:155-62
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