Program in Cellular and Molecular Biology, University of Wisconsin-Madison, Madison, Wisconsin 53705, USA.
J Neurochem. 2010 Dec;115(6):1409-20. doi: 10.1111/j.1471-4159.2010.07045.x. Epub 2010 Nov 4.
Myelination of peripheral nerves by Schwann cells depends upon a gene regulatory network controlled by early growth response Egr2/Krox20, which is specifically required for Schwann cells to initiate and maintain myelination. To elucidate the mechanism by which Egr2 regulates gene expression during myelination, we have performed chromatin immunoprecipitation analysis on myelinating rat sciatic nerve in vivo. The resulting samples were applied to a tiled microarray consisting of a broad spectrum of genes that are activated or repressed in Egr2-deficient mice. The results show extensive binding within myelin-associated genes, as well as some genes that become repressed in myelinating Schwann cells. Many of the Egr2 peaks coincide with regions of open chromatin, which is a marker of enhancer regions. In addition, further analysis showed that there is substantial colocalization of Egr2 binding with Sox10, a transcription factor required for Schwann cell specification and other stages of Schwann cell development. Finally, we have found that Egr2 binds to promoters of several lipid biosynthetic genes, which is consistent with their dramatic up-regulation during the formation of lipid-rich myelin. Overall, this analysis provides a locus-wide profile of Egr2 binding patterns in major myelin-associated genes using myelinating peripheral nerve.
许旺细胞对周围神经的髓鞘形成依赖于一个由早期生长反应 Egr2/Krox20 控制的基因调控网络,该网络专门用于许旺细胞启动和维持髓鞘形成。为了阐明 Egr2 在髓鞘形成过程中调节基因表达的机制,我们对体内髓鞘形成的大鼠坐骨神经进行了染色质免疫沉淀分析。将得到的样本应用于由广泛激活或抑制 Egr2 缺陷型小鼠的基因组成的平铺微阵列。结果表明,Egr2 在髓鞘相关基因中有广泛的结合,以及一些在髓鞘形成许旺细胞中被抑制的基因。许多 Egr2 峰与开放染色质区域重合,这是增强子区域的标志。此外,进一步的分析表明,Egr2 结合与 Sox10 有大量的共定位,Sox10 是许旺细胞特化和其他许旺细胞发育阶段所必需的转录因子。最后,我们发现 Egr2 结合到几个脂质生物合成基因的启动子上,这与它们在富含脂质的髓鞘形成过程中的显著上调一致。总的来说,这项分析提供了使用髓鞘形成的周围神经对主要髓鞘相关基因中 Egr2 结合模式的全基因座图谱。