Friedrich Ralf P, Schlierf Beate, Tamm Ernst R, Bösl Michael R, Wegner Michael
Institut für Biochemie, Universität Erlangen, Fahrstrasse 17, 91054 Erlangen, Germany.
Mol Cell Biol. 2005 Mar;25(5):1821-9. doi: 10.1128/MCB.25.5.1821-1829.2005.
For differentiation, Schwann cells rely on the class III POU domain transcription factor Oct-6, which is expressed transiently when Schwann cells have established a one-to-one relation with axons but have not yet started to myelinate. Loss of Oct-6 leads to a transient arrest in this promyelinating stage and a delay in myelination. Although the closely related POU domain protein Brn-2 is coexpressed with Oct-6 in Schwann cells, its loss has only mild consequences. Combined loss of both POU domain proteins, in contrast, dramatically increases the myelination delay, raising the question of how related POU domain proteins compare to each other in their activities. Here, we have replaced Oct-6 expression in the mouse with expression of the class III POU domain protein Brn-1. Although this protein is not normally expressed in Schwann cells, Brn-1 was capable of fully replacing Oct-6. Brn-1 efficiently induced Krox-20 expression as a prerequisite for myelination. Onset and extent of myelination were also indistinguishable from that of the wild type in mice that carried only Brn-1 instead of Oct-6 alleles. Similar to Oct-6, Brn-1 down-regulated its own expression at later stages of myelination. Thus, class III POU domain proteins can fully replace each other in Schwann cell development.
为了实现分化,施万细胞依赖于III类POU结构域转录因子Oct-6,当施万细胞与轴突建立一对一关系但尚未开始髓鞘化时,Oct-6会短暂表达。Oct-6的缺失会导致这个促髓鞘化阶段的短暂停滞以及髓鞘化延迟。尽管密切相关的POU结构域蛋白Brn-2在施万细胞中与Oct-6共表达,但其缺失仅产生轻微后果。相比之下,两种POU结构域蛋白的共同缺失会显著增加髓鞘化延迟,这就引发了一个问题,即相关的POU结构域蛋白在活性方面如何相互比较。在这里,我们用III类POU结构域蛋白Brn-1的表达取代了小鼠体内Oct-6的表达。尽管这种蛋白通常不在施万细胞中表达,但Brn-1能够完全替代Oct-6。Brn-1有效地诱导了Krox-20的表达,这是髓鞘化的先决条件。在仅携带Brn-1而非Oct-6等位基因的小鼠中,髓鞘化的起始和程度与野生型也没有区别。与Oct-6相似,Brn-1在髓鞘化后期下调了自身的表达。因此,III类POU结构域蛋白在施万细胞发育过程中可以完全相互替代。