Abstract
The controlling factors that prompt mature oligodendrocytes to myelinate axons are largely undetermined. In this study, we used a forward genetics approach to identify a mutant mouse strain characterized by the absence of CNS myelin despite the presence of abundant numbers of late-stage, process-extending oligodendrocytes. Through linkage mapping and complementation testing, we identified the mutation as a single nucleotide insertion in the gene encoding zinc finger protein 191 (Zfp191), which is a widely expressed, nuclear-localized protein that belongs to a family whose members contain both DNA-binding zinc finger domains and protein-proteininteracting SCAN domains. Zfp191 mutants express an array of myelin-related genes at significantly reduced levels, and our in vitro and in vivo data indicate that mutant ZFP191 acts in a cell-autonomous fashion to disrupt oligodendrocyte function. Therefore, this study demonstrates that ZFP191 is required for the myelinating function of differentiated oligodendrocytes.
Original language | English (US) |
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Pages (from-to) | 301-311 |
Number of pages | 11 |
Journal | Genes and Development |
Volume | 24 |
Issue number | 3 |
DOIs | |
State | Published - Feb 1 2010 |
Keywords
- Conditional allele
- Forward genetics
- Hypomyelination
- Mouse mutant
- Scan domain
- Zinc finger protein