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The Transcription Factors Sox10 and Myrf Define an Essential Regulatory Network Module in Differentiating Oligodendrocytes

Overview
Journal PLoS Genet
Specialty Genetics
Date 2013 Nov 9
PMID 24204311
Citations 106
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Abstract

Myelin is essential for rapid saltatory conduction and is produced by Schwann cells in the peripheral nervous system and oligodendrocytes in the central nervous system. In both cell types the transcription factor Sox10 is an essential component of the myelin-specific regulatory network. Here we identify Myrf as an oligodendrocyte-specific target of Sox10 and map a Sox10 responsive enhancer to an evolutionarily conserved element in intron 1 of the Myrf gene. Once induced, Myrf cooperates with Sox10 to implement the myelination program as evident from the physical interaction between both proteins and the synergistic activation of several myelin-specific genes. This is strongly reminiscent of the situation in Schwann cells where Sox10 first induces and then cooperates with Krox20 during myelination. Our analyses indicate that the regulatory network for myelination in oligodendrocytes is organized along similar general principles as the one in Schwann cells, but is differentially implemented.

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References
1.
Liu Z, Hu X, Cai J, Liu B, Peng X, Wegner M . Induction of oligodendrocyte differentiation by Olig2 and Sox10: evidence for reciprocal interactions and dosage-dependent mechanisms. Dev Biol. 2006; 302(2):683-93. DOI: 10.1016/j.ydbio.2006.10.007. View

2.
Bondurand N, Girard M, Pingault V, Lemort N, Dubourg O, Goossens M . Human Connexin 32, a gap junction protein altered in the X-linked form of Charcot-Marie-Tooth disease, is directly regulated by the transcription factor SOX10. Hum Mol Genet. 2001; 10(24):2783-95. DOI: 10.1093/hmg/10.24.2783. View

3.
Wissmuller S, Kosian T, Wolf M, Finzsch M, Wegner M . The high-mobility-group domain of Sox proteins interacts with DNA-binding domains of many transcription factors. Nucleic Acids Res. 2006; 34(6):1735-44. PMC: 1421504. DOI: 10.1093/nar/gkl105. View

4.
Stolt C, Rehberg S, Ader M, Lommes P, Riethmacher D, Schachner M . Terminal differentiation of myelin-forming oligodendrocytes depends on the transcription factor Sox10. Genes Dev. 2002; 16(2):165-70. PMC: 155320. DOI: 10.1101/gad.215802. View

5.
McCarthy K, de Vellis J . Preparation of separate astroglial and oligodendroglial cell cultures from rat cerebral tissue. J Cell Biol. 1980; 85(3):890-902. PMC: 2111442. DOI: 10.1083/jcb.85.3.890. View