Transgenic complementation of rumpshaker with wild type proteolipid protein

Barrie, Jennifer Ann (2008) Transgenic complementation of rumpshaker with wild type proteolipid protein. MSc(R) thesis, University of Glasgow.

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Printed Thesis Information: https://eleanor.lib.gla.ac.uk/record=b2645522

Abstract

Mutations in the x-linked myelin proteolipid protein 1 gene (PLP1) cause the heterogeneous syndromes of Pelizaeus Merzbacher disease (PMD) and Spastic paraplegia type 2(SPG2) in man (Hudson et al., 2004). A single base change mutation in our spontaneous mouse model rumpshaker (Plpjp-rsh)(Ile186Thr) (Schneider et al., 1992) generates a misfolded protein resulting in dysmyelination and increased numbers of apoptotic oligodendrocytes. The phenotype varies from mild on the original C3H background to lethal when backcrossed onto the C57BL/6 mouse strain (Al-Saktawi et al., 2003). Utilising the more severe variant we sought to ameliorate the lethal phenotype by transgenic complementation with wild type Plp1 (Readhead et al., 1994) to normalise the levels of proteolipid protein (PLP) and it’s smaller isoform DM20.
The presence of the wild type protein improves the survival of the mice, decreases oligodendrocyte apoptosis and restores normal periodicity to the myelin, however hypomyelination remains severe. Although the PLP/DM20 level is restored to normal the level of myelin basic protein remains low. In addition the presence of the wild type protein does not ameliorate the unfolded protein response induced by the rumpshaker PLP/DM20.

Item Type: Thesis (MSc(R))
Qualification Level: Masters
Keywords: PLP,rumpshaker,transgenic complementation,
Subjects: Q Science > QH Natural history > QH301 Biology
S Agriculture > SF Animal culture > SF600 Veterinary Medicine
Colleges/Schools: College of Medical Veterinary and Life Sciences > School of Biodiversity, One Health & Veterinary Medicine
Supervisor's Name: Griffiths, Professor Ian,R
Date of Award: 2008
Depositing User: Mrs Jennifer Barrie
Unique ID: glathesis:2008-368
Copyright: Copyright of this thesis is held by the author.
Date Deposited: 14 Nov 2008
Last Modified: 10 Dec 2012 13:18
URI: https://theses.gla.ac.uk/id/eprint/368

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