Our long term goal is to define the characteristic cellular and developmental role or roles of spectrin and understand how spectrin molecules contribute to specific cellular functions. We believe our long term goal can be attained by using a model system, Drosophila melanogaster, that can be investigated at both the cellular and the tissue level using a combination of biochemical, structural and genetic approaches. Antibodies will be used to study the distribution and expression of spectrin both in cell culture and during development and to identify DNA sequences that express Drosophila spectrin. Clones of these DNA sequences will be used to map the physical location of the spectrin coding sequences on the genetic map of Drosophila and classical genetic analysis and in vitro mutant production will then be carried out. The mutants will be used to investigate spectrin function in vivo and to determine the effects of the complete absence of functional spectrin. The clones will also be used together with the technology of anti-sense inhibition of expression to inhibit spectrin expression in cultured cells so that we may probe the effects of the absence of functional spectrin or the consequences of mutant spectrin expression in cultured cells. Spectrin is present in nearly all human cells but the health consequences of defective spectrin expression have only been explored in erythrocytes. The proposed experiments should provide an in-depth understanding of spectrin's role in non- erythroid cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM039686-02
Application #
3296787
Study Section
Cellular Biology and Physiology Subcommittee 1 (CBY)
Project Start
1988-06-01
Project End
1993-05-31
Budget Start
1989-06-01
Budget End
1990-05-31
Support Year
2
Fiscal Year
1989
Total Cost
Indirect Cost
Name
Harvard University
Department
Type
Schools of Arts and Sciences
DUNS #
071723621
City
Cambridge
State
MA
Country
United States
Zip Code
02138
Lee, J K; Brandin, E; Branton, D et al. (1997) alpha-Spectrin is required for ovarian follicle monolayer integrity in Drosophila melanogaster. Development 124:353-62
Lue, R A; Brandin, E; Chan, E P et al. (1996) Two independent domains of hDlg are sufficient for subcellular targeting: the PDZ1-2 conformational unit and an alternatively spliced domain. J Cell Biol 135:1125-37
Deng, H; Lee, J K; Goldstein, L S et al. (1995) Drosophila development requires spectrin network formation. J Cell Biol 128:71-9
Zhang, P; Talluri, S; Deng, H et al. (1995) Solution structure of the pleckstrin homology domain of Drosophila beta-spectrin. Structure 3:1185-95
Lee, J K; Coyne, R S; Dubreuil, R R et al. (1993) Cell shape and interaction defects in alpha-spectrin mutants of Drosophila melanogaster. J Cell Biol 123:1797-809
Byers, T J; Brandin, E; Lue, R A et al. (1992) The complete sequence of Drosophila beta-spectrin reveals supra-motifs comprising eight 106-residue segments. Proc Natl Acad Sci U S A 89:6187-91
Winograd, E; Hume, D; Branton, D (1991) Phasing the conformational unit of spectrin. Proc Natl Acad Sci U S A 88:10788-91
Dubreuil, R R (1991) Structure and evolution of the actin crosslinking proteins. Bioessays 13:219-26
Dubreuil, R R; Brandin, E; Reisberg, J H et al. (1991) Structure, calmodulin-binding, and calcium-binding properties of recombinant alpha spectrin polypeptides. J Biol Chem 266:7189-93
Dubreuil, R R; Byers, T J; Stewart, C T et al. (1990) A beta-spectrin isoform from Drosophila (beta H) is similar in size to vertebrate dystrophin. J Cell Biol 111:1849-58

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