| Literature DB >> 20080941 |
Shen Yi B Howng1, Robin L Avila, Ben Emery, Maria Traka, Wensheng Lin, Trent Watkins, Susan Cook, Roderick Bronson, Muriel Davisson, Ben A Barres, Brian Popko.
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-protein-interacting 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.Entities:
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Year: 2010 PMID: 20080941 PMCID: PMC2811831 DOI: 10.1101/gad.1864510
Source DB: PubMed Journal: Genes Dev ISSN: 0890-9369 Impact factor: 11.361