Mandemakers W, Zwart R, Jaegle M, Walbeehm E, Visser P, Grosveld F, Meijer D
Department of Cell Biology and Genetics and Department of Plastic Surgery, Erasmus University Rotterdam, PO Box 1738, 3000 DR Rotterdam, The Netherlands.
EMBO J. 2000 Jun 15;19(12):2992-3003. doi: 10.1093/emboj/19.12.2992.
The POU domain transcription factor Oct-6 is a major regulator of Schwann cell differentiation and myelination. During nerve development and regeneration, expression of Oct-6 is under the control of axonal signals. Identification of the cis-acting elements necessary for Oct-6 gene regulation is an important step in deciphering the complex signalling between Schwann cells and axons governing myelination. Here we show that a fragment distal to the Oct-6 gene, containing two DNase I-hypersensitive sites, acts as the Oct-6 Schwann cell-specific enhancer (SCE). The SCE is sufficient to drive spatially and temporally correct expression, during both normal peripheral nerve development and regeneration. We further demonstrate that a tagged version of Oct-6, driven by the SCE, rescues the peripheral nerve phenotype of Oct-6-deficient mice. Thus, our isolation and characterization of the Oct-6 SCE provides the first description of a cis-acting genetic element that responds to converging signalling pathways to drive myelination in the peripheral nervous system.
POU结构域转录因子Oct-6是雪旺细胞分化和髓鞘形成的主要调节因子。在神经发育和再生过程中,Oct-6的表达受轴突信号的控制。鉴定Oct-6基因调控所需的顺式作用元件是破译雪旺细胞与轴突之间控制髓鞘形成的复杂信号的重要一步。在此,我们表明Oct-6基因远端的一个片段,包含两个DNase I超敏位点,作为Oct-6雪旺细胞特异性增强子(SCE)。在正常外周神经发育和再生过程中,SCE足以驱动空间和时间上正确的表达。我们进一步证明,由SCE驱动的Oct-6标记版本挽救了Oct-6缺陷小鼠的外周神经表型。因此,我们对Oct-6 SCE的分离和表征首次描述了一种顺式作用遗传元件,它响应汇聚的信号通路以驱动外周神经系统中的髓鞘形成。