Myelination is a complex developmental process seen only in the nervous system, whereby a specialized glial membrane, the myelin sheath, is elaborated around axons. In mice there are a number of neurological mutants whose phenotypic expression is abnormal myelination. One of those mutants, the shiverer mouse, has been shown to have a partial deletion of the myelin basic protein (MBP) gene. This single gene codes for four different forms of MBP, a major myelin protein. The first objective of this proposal is to identify in vitro those cis-acting regulatory elements responsible for the expression of MBP in the oligodendrocyte. A second objective is to utilize methods for the production of transgenic systems to transfer the cloned MBP gene into the genetic background found in the shiverer mouse. A genomic clone containing the entire genomic structure of the MBP gene and a cDNA clone for the 18.5kd form of MBP will be expressed in transgenic animals using the flanking regions of the MBP gene. These transgenic systems will be used for the following purposes: (1) to identify those cis elements involved in the high level expression of the myelin basic proteins in the oligodendrocyte; (2) to examine which tissues and cell types possess the trans factors necessary for utilization of these cis elements; (3) to analyze the splicing patterns that are responsible for the different forms of MBP; and (4) to study whether multiple forms of MBP are necessary for myelination, by expressing only one form of MBP in a transgenic shiverer mouse. The objective of this study is to utilize molecular biology and genetic mutations affecting myelination to advance the understanding of the biology of myelination. This understanding will be crucial to the future determination of how this biology is altered in the dysmyelinating and demyelinating disorders of man.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Clinical Investigator Award (CIA) (K08)
Project #
5K08NS001163-03
Application #
3083919
Study Section
Neurological Disorders Program Project Review B Committee (NSPB)
Project Start
1986-12-01
Project End
1991-11-30
Budget Start
1988-12-01
Budget End
1989-11-30
Support Year
3
Fiscal Year
1989
Total Cost
Indirect Cost
Name
California Institute of Technology
Department
Type
Schools of Arts and Sciences
DUNS #
078731668
City
Pasadena
State
CA
Country
United States
Zip Code
91125
Puckett, C; Concannon, P; Casey, C et al. (1991) Genomic structure of the human prion protein gene. Am J Hum Genet 49:320-9
Puckett, C; Gomez, C M; Korenberg, J R et al. (1991) Molecular cloning and chromosomal localization of one of the human glutamate receptor genes. Proc Natl Acad Sci U S A 88:7557-61
Popko, B; Puckett, C; Lai, E et al. (1987) Myelin deficient mice: expression of myelin basic protein and generation of mice with varying levels of myelin. Cell 48:713-21
Bergmann, K J; Mendoza, M R; Yahr, M D (1987) Parkinson's disease and long-term levodopa therapy. Adv Neurol 45:463-7