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Effects of Rumpshaker Mutation on CNS Myelin Composition and Structure
Author(s) -
Karthigasan J.,
Evans E. L.,
Vouyiouklis D. A.,
Inouye H.,
Borenshteyn N.,
Ramamurthy G. V.,
Kirschner D. A.
Publication year - 1996
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1046/j.1471-4159.1996.66010338.x
Subject(s) - myelin , mutant , chemistry , microbiology and biotechnology , optic nerve , electron microscope , proteolipid protein 1 , densitometry , polyacrylamide gel electrophoresis , mutation , gene , biochemistry , biology , myelin basic protein , central nervous system , endocrinology , anatomy , medicine , enzyme , physics , optics
Myelinated CNS tissues from homozygous/hemizygous and heterozygous jimpy rumpshaker jp rsh mutant mice were examined to determine the consequences on myelin structure of this mutation in the proteolipid protein (PLP) gene. Polyacrylamide gel electrophoresis and immunoblotting of brain homogenates confirmed that there was a decrease in PLP levels on the B6C3 genetic background onto which this gene was bred. We also observed an increase in level of a protein band that could correspond to the uncharacterized 10‐kDa PLP previously reported in jp rsh mice on an Rb(1.3) 1Bnr background. High‐performance TLC and densitometry of lipids from brain homogenate and isolated myelin revealed a decrease in content of cerebrosides and sulfatides. Electron microscopy on optic nerves revealed that normal radial component is retained in jp rsh myelin, further substantiating that PLP is not a component of this junctional complex. X‐raydiffraction measurements on unfixed optic nerves showed that the jp rsh period is 5–10 Å larger than normal. Moreover, jp rsh optic nerve myelin was unstable, as evidenced by a continual increase in the period postdissection. jp rsh myelin that was equilibrated at varying pH and ionic strength typically had a larger than normal period under all conditions (both swelling and compacting). Our findings thus demonstrate that the biochemical abnormalities in the jp rsh mutant correlate with a wider periodicity and less stable packing of the myelin.