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Research Article Free access | 10.1172/JCI1807

Neurological disturbances, premature lethality, and central myelination deficiency in transgenic mice overexpressing the homeo domain transcription factor Oct-6.

N A Jensen, K M Pedersen, J E Celis, and M J West

Department of Medical Biochemistry, University of Aarhus, 8000 Aarhus C, Denmark. naj@biobase.dk

Find articles by Jensen, N. in: PubMed | Google Scholar

Department of Medical Biochemistry, University of Aarhus, 8000 Aarhus C, Denmark. naj@biobase.dk

Find articles by Pedersen, K. in: PubMed | Google Scholar

Department of Medical Biochemistry, University of Aarhus, 8000 Aarhus C, Denmark. naj@biobase.dk

Find articles by Celis, J. in: PubMed | Google Scholar

Department of Medical Biochemistry, University of Aarhus, 8000 Aarhus C, Denmark. naj@biobase.dk

Find articles by West, M. in: PubMed | Google Scholar

Published March 15, 1998 - More info

Published in Volume 101, Issue 6 on March 15, 1998
J Clin Invest. 1998;101(6):1292–1299. https://doi.org/10.1172/JCI1807.
© 1998 The American Society for Clinical Investigation
Published March 15, 1998 - Version history
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Abstract

Pit, Oct, Unc (POU) homeo domain transcription factors have been implicated in various developmental processes, including cell division, differentiation, specification, and survival of specific cell types. Although expression of the transcription factor Oct-6 in oligodendroglia is confined to the promyelin stage and is downregulated at the myelin stage of development, the effect of Oct-6 overexpression on oligodendrocyte development has not been established. Here we show that transgenic animals overexpressing Oct-6 at late oligodendrocyte development develop a severe neurologic syndrome characterized by action tremors, recurrent seizures, and premature death. Axons in the central nervous system of Oct-6 transgenics were hypomyelinated, hypermyelinated, or dysmyelinated, and ultrastructural analyses suggested that myelin formation was premature. The vulnerability of developing oligodendroglia to Oct-6 deregulation provides evidence that the POU factor may play a direct role in myelin disease pathogenesis in the mammalian CNS.

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