4.7 Article

ZFP191 is required by oligodendrocytes for CNS myelination

Journal

GENES & DEVELOPMENT
Volume 24, Issue 3, Pages 301-311

Publisher

COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1101/gad.1864510

Keywords

Mouse mutant; forward genetics; hypomyelination; conditional allele; zinc finger protein; scan domain

Funding

  1. Myelin Repair Foundation
  2. NIH [R01NS067550]
  3. NIH/NCRR [P40 RR001183]

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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.

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