Dataset Information


Genome-wide mapping of Olig2 targets in primary oligodendrocytes

ABSTRACT: Myelination by oligodendrocytes in the central nervous system (CNS) is essential for proper brain function, yet the molecular determinants that control this process remain poorly understood. The basic helix-loop-helix transcription factors Olig1 and Olig2 promote myelination, whereas bone morphogenetic protein (BMP) and Wnt/β-catenin signaling inhibit myelination. Here we show that these opposing regulators of myelination are functionally linked by the Olig1/2 common target Smad-interacting protein-1 (Sip1). We demonstrate that Sip1 is an essential modulator of CNS myelination. Sip1 represses differentiation inhibitory signals by antagonizing BMP receptor-activated Smad activity while activating crucial oligodendrocyte-promoting factors. Importantly, a key Sip1-activated target, Smad7, is required for oligodendrocyte differentiation and partially rescues differentiation defects caused by Sip1 loss. Smad7 promotes myelination by blocking the BMP- and β-catenin-negative regulatory pathways. Thus, our findings reveal that Sip1-mediated antagonism of inhibitory signaling is critical for promoting CNS myelination and point to new mediators for myelin repair. Overall design: ChIP-seq was performed to identify Olig2 direct target genes in oligodendrocytes during oligodendrocyte differentiation.

INSTRUMENT(S): Illumina Genome Analyzer (Rattus norvegicus)

ORGANISM(S): Rattus norvegicus  

SUBMITTER: Qing Richard Lu  




Similar Datasets

2012-08-31 | E-GEOD-40506 | ArrayExpress
2012-08-31 | E-GEOD-40510 | ArrayExpress
| GSE119815 | GEO
| GSE119814 | GEO
2013-01-20 | E-GEOD-42447 | ArrayExpress
| GSE119812 | GEO
| GSE101535 | GEO
2016-02-19 | E-GEOD-65119 | ArrayExpress
| GSE103324 | GEO
| GSE82210 | GEO