Chapter

Myelin-specific genes and their mutations in the mouse

Klaus-Armin Nave

in Glial Cell Development

Published in print November 1997 | ISBN: 9781872748542
Published online March 2012 | e-ISBN: 9780191724367 | DOI: http://dx.doi.org/10.1093/acprof:oso/9781872748542.003.0008

Series: The Molecular and Cellular Neurobiology Series

Myelin-specific genes and their mutations in the mouse

Show Summary Details

Preview

Myelination depends on the co-ordinate expression of a battery of structural proteins which are responsible for the architecture of compacted myelin. Mutations of myelin genes illustrate how development proceeds in the absence of the corresponding myelin proteins (and often in the presence of the mutant gene product). These observations allow the reconstruction of myelin protein functions, and merge slowly into a larger picture. Whereas some hypotheses of a structure-function relationship have been confirmed (e.g., for MBP and PO), the mutations in the genes for PLP, PMP22, and MAG are more difficult to interpret. Both, the unexpected phenotype and the lack thereof will lead to modifications of existing models and suggest specific experiments often times in more simplified systems. Some of the mouse mutants have become accurate models for human dysmyelinating disease (Pelizaeus–Merzbacher disease, Charcot–Marie–Tooth disease). Experimental mouse genetics will continue to be an important tool for both developmental neurobiology and clinical research.

Keywords: myelination; genetic mutations; myelin proteins; PLP; PMP22; MAG

Chapter.  10489 words.  Illustrated.

Subjects: Neuroscience

Full text: subscription required

How to subscribe Recommend to my Librarian

Buy this work at Oxford University Press »

Users without a subscription are not able to see the full content. Please, subscribe or login to access all content.