Control of myelination in Schwann cells:: a Krox20 cis-regulatory element integrates Oct6, Brn2 and Sox10 activities

被引:135
作者
Ghislain, J [1 ]
Charnay, P [1 ]
机构
[1] INSERM, U368, Ecole Normale Super, F-75230 Paris 05, France
关键词
Krox20/Egr2; Oct6/Tst1/SCIP/Pou3f1/Oft-6; Brn2/N-Oct3/Pou3f2/Oft-7; myelination; peripheral nervous system; transcriptional regulation;
D O I
10.1038/sj.embor.7400573
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Myelination in Schwann cells is governed by several transcription factors, including the POU proteins Oct6 and Brn2, the high mobility group protein Sox10 and the zinc-finger protein Krox20. How the function of these factors is integrated in the control of myelination has not been established. Previously, we identified an enhancer element controlling Krox20 expression throughout myelination in Schwann cells. In this paper, cell culture experiments were combined with transgenesis to identify transcription factors acting directly upstream of Krox20. The results show that during the promyelin-myelin transition, Krox20 expression is directly activated by Oct6 and Brn2 acting on this enhancer. In addition, the enhancer-dependent synergism between these POU proteins and Sox10 suggests that Krox20 expression requires this combination of factors. These results resolve previous controversy concerning the mechanism of action of Oct6 and Brn2 during myelination and provide an explanation for myelin deficiencies in Waardenberg-Hirschsprung disease patients whereby Sox10 mutations could lead to a loss of Krox20 expression.
引用
收藏
页码:52 / 58
页数:7
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