Neurofilaments are major, but nonetheless poorly understood, neuron specific 10nm filaments. They are composed of three subunit proteins usually referred to as NF-1, NF-M and NF-H. NF-M and NF-H differ from other characterized 10 nm filament proteins in that they contain long heavily phosphorylated carboxyterminal extensions. These carboxyterminal regions have recently been shown to contain two distinct segments, probably corresponding to two types of functional domain. The first contains multiple repeats of 5-8 amino acid segments each containing the sequence lysine-serine-proline, and is here referred to as KSP segment. The second domain, at the extreme carboxyterminus, has a high content of lysine and glutamic acid, and is called the KE segment. In the present proposal I wish to test two hypotheses I have proposed which assign functions to these unusual segments. These hypotheses are; 1. That some or all of the KE segments are responsible for a strong interaction which binds neurofilaments together into bundles. i will search for such an interaction using isolated KE domains and fusion proteins containing KE segments. Detection of a binding interaction will be followed by characterization of his interaction in detail and proof that this interaction is actually responsible for filament bundling in vivo. 2. That phosphorylation of the KSP regions of the NF-H and NF-M molecules is responsible for modulating the spacing of neurofilaments from one another in bundles. Evidence for or against this hypothesis will not detract from the importance of identifying and characterizing the KSP kinase activity, which may phosphorylate other axonal proteins besides neurofilaments and appears to change in activity following neuronal injury and in various disease states. I will make use of the new sequence data to isolate this enzyme. In summary the studies proposed will increase our understanding of the function of two unusual regions of the neurofilament molecules, and will characterize a kinase activity of great potential importance in recovery from injury and in the maintenance of differences between axons and dendrites.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS022695-06
Application #
3405471
Study Section
Neurological Sciences Subcommittee 1 (NLS)
Project Start
1985-07-01
Project End
1993-06-30
Budget Start
1991-02-01
Budget End
1993-06-30
Support Year
6
Fiscal Year
1991
Total Cost
Indirect Cost
Name
University of Florida
Department
Type
Schools of Medicine
DUNS #
073130411
City
Gainesville
State
FL
Country
United States
Zip Code
32611
Errante, L; Tang, D; Gardon, M et al. (1998) The intermediate filament protein peripherin is a marker for cerebellar climbing fibres. J Neurocytol 27:69-84
Lu, D; Yang, H; Shaw, G et al. (1998) Angiotensin II-induced nuclear targeting of the angiotensin type 1 (AT1) receptor in brain neurons. Endocrinology 139:365-75
Wang, D S; Deng, T; Shaw, G (1997) Membrane binding and enzymatic activation of a Dbl homology domain require the neighboring pleckstrin homology domain. Biochem Biophys Res Commun 234:183-9
Shaw, G; Miller, R; Wang, D S et al. (1997) Characterization of additional casein kinase I sites in the C-terminal ""tail"" region of chicken and rat neurofilament-M. J Neurochem 69:1729-37
Wang, D S; Miller, R; Shaw, R et al. (1996) The pleckstrin homology domain of human beta I sigma II spectrin is targeted to the plasma membrane in vivo. Biochem Biophys Res Commun 225:420-6
Benson, D L; Mandell, J W; Shaw, G et al. (1996) Compartmentation of alpha-internexin and neurofilament triplet proteins in cultured hippocampal neurons. J Neurocytol 25:181-96
Shaw, G (1996) The pleckstrin homology domain: an intriguing multifunctional protein module. Bioessays 18:35-46
Hollander, B A; Bennett, G S; Shaw, G (1996) Localization of sites in the tail domain of the middle molecular mass neurofilament subunit phosphorylated by a neurofilament-associated kinase and by casein kinase I. J Neurochem 66:412-20
Wang, D S; Shaw, G (1995) The association of the C-terminal region of beta I sigma II spectrin to brain membranes is mediated by a PH domain, does not require membrane proteins, and coincides with a inositol-1,4,5 triphosphate binding site. Biochem Biophys Res Commun 217:608-15
Wang, D S; Shaw, R; Hattori, M et al. (1995) Binding of pleckstrin homology domains to WD40/beta-transducin repeat containing segments of the protein product of the Lis-1 gene. Biochem Biophys Res Commun 209:622-9

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