The myelination-associated G protein-coupled receptor 37 is regulated by Zfp488, Nkx2.2, and Sox10 during oligodendrocyte differentiation
- PMID: 38546197
- DOI: 10.1002/glia.24530
The myelination-associated G protein-coupled receptor 37 is regulated by Zfp488, Nkx2.2, and Sox10 during oligodendrocyte differentiation
Abstract
Oligodendrocyte differentiation and myelination in the central nervous system are controlled and coordinated by a complex gene regulatory network that contains several transcription factors, including Zfp488 and Nkx2.2. Despite the proven role in oligodendrocyte differentiation little is known about the exact mode of Zfp488 and Nkx2.2 action, including their target genes. Here, we used overexpression of Zfp488 and Nkx2.2 in differentiating CG4 cells to identify aspects of the oligodendroglial expression profile that depend on these transcription factors. Although both transcription factors are primarily described as repressors, the detected changes argue for an additional function as activators. Among the genes activated by both Zfp488 and Nkx2.2 was the G protein-coupled receptor Gpr37 that is important during myelination. In agreement with a positive effect on Gpr37 expression, downregulation of the G protein-coupled receptor was observed in Zfp488- and in Nkx2.2-deficient oligodendrocytes in the mouse. We also identified several potential regulatory regions of the Gpr37 gene. Although Zfp488 and Nkx2.2 both bind to one of the regulatory regions downstream of the Gpr37 gene in vivo, none of the regulatory regions was activated by either transcription factor alone. Increased activation by Zfp488 or Nkx2.2 was only observed in the presence of Sox10, a transcription factor continuously present in oligodendroglial cells. Our results argue that both Zfp488 and Nkx2.2 also act as transcriptional activators during oligodendrocyte differentiation and cooperate with Sox10 to allow the expression of Gpr37 as a modulator of the myelination process.
Keywords: Sox; glia; myelin; seven transmembrane receptor; transcription factor.
© 2024 The Authors. GLIA published by Wiley Periodicals LLC.
References
REFERENCES
-
- Aberle, T., Piefke, S., Hillgartner, S., Tamm, E. R., Wegner, M., & Küspert, M. (2022). Transcription factor Zfp276 drives oligodendroglial differentiation and myelination by switching off the progenitor cell program. Nucleic Acids Research, 50, 1951–1968. https://doi.org/10.1093/nar/gkac042
-
- Aprato, J., Sock, E., Weider, M., Elsesser, O., Fröb, F., & Wegner, M. (2020). Myrf guides target gene selection of transcription factor Sox10 during oligodendroglial development. Nucleic Acids Research, 48, 1254–1270. https://doi.org/10.1093/nar/gkz1158
-
- Bernhardt, C., Sock, E., Fröb, F., Hillgärtner, S., Nemer, M., & Wegner, M. (2022). KLF9 and KLF13 transcription factors boost myelin gene expression in oligodendrocytes as partners of SOX10 and MYRF. Nucleic Acids Research, 50, 11509–11528. https://doi.org/10.1093/nar/gkac953
-
- Bujalka, H., Koenning, M., Jackson, S., Perreau, V. M., Pope, B., Hay, C. M., Hill, A. F., Wegner, M., Srinivasan, R., Svaren, J., Willingham, M., Barres, B. A., & Emery, B. (2013). MYRF is a membrane‐associated transcription factor that autoproteolytically cleaves to directly activate myelin genes. PLoS Biology, 11, e1001625.
-
- Dessaud, E., Yang, L. L., Hill, K., Cox, B., Ulloa, F., Ribeiro, A., Mynett, A., Novitch, B. G., & Briscoe, J. (2007). Interpretation of the sonic hedgehog morphogen gradient by a temporal adaptation mechanism. Nature, 450, 717–720. https://doi.org/10.1038/nature06347
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Molecular Biology Databases
Miscellaneous