Abstract
While an important role for the POU domain transcription factor Oct-6 in the developing peripheral nerve has been well established, studies into its exact role in nerve development and regeneration have been hampered by the high mortality rate of newborn Oct-6 mutant animals. In this study we have generated a Schwann cell-specific Oct-6 allele through deletion of the Schwann cell-specific enhancer element (SCE) in the Oct-6 locus. Analysis of mice homozygous for this allele (ΔSCE allele) reveals that rate-limiting levels of Oct-6 in Schwann cells are dependent on the SCE and that this element does not contribute to Oct-6 regulation in other cell types. We demonstrate a Schwann cell autonomous function for Oct-6 during nerve development as well as in regenerating nerve. Additionally, we show that Krox-20, an important regulatory target of Oct-6 in Schwann cells, is activated, with delayed kinetics, through an Oct-6-independent mechanism in these mice.
| Original language | English |
|---|---|
| Pages (from-to) | 4612-4620 |
| Number of pages | 9 |
| Journal | EMBO Journal |
| Volume | 21 |
| Issue number | 17 |
| DOIs | |
| Publication status | Published - 2 Sept 2002 |
Keywords / Materials (for Non-textual outputs)
- Enhancer
- Glia
- Myelin
- Oct-6
- POU domain