Cepek K L, Chasman D I, Sharp P A
Center for Cancer Research, Massachusetts Institute of Technology, Cambridge 02139, USA.
Genes Dev. 1996 Aug 15;10(16):2079-88. doi: 10.1101/gad.10.16.2079.
B-cell-specific transcription of immunoglobulin genes is mediated by the interaction of a POU domain containing transcription factor Oct-1 or Oct-2, with the B-cell-specific coactivator OCA-B (Bob-1, OBF-1) and a prototype octamer element. We find that OCA-B binds DNA directly in the major groove between the two subdomains of the POU domain, requiring both an A at the fifth position of the octamer element and contact with the POU domain. An amino-terminal fragment of OCA-B binds the octamer site in the absence of a POU domain with the same sequence specificity. Coactivator OCA-B may undergo a POU-dependent conformational change that exposes its amino terminus, allowing it to recognize specific DNA sequences in the major groove within the binding site for Oct-1 or Oct-2. The recognition of both the POU domain and the octamer sequence by OCA-B provides a mechanism for differential regulation of octamer sites containing genes by the ubiquitous factor Oct-1.
免疫球蛋白基因的B细胞特异性转录是由含POU结构域的转录因子Oct-1或Oct-2与B细胞特异性共激活因子OCA-B(Bob-1、OBF-1)及一个典型的八聚体元件相互作用介导的。我们发现,OCA-B直接结合于POU结构域两个亚结构域之间的大沟中的DNA,这既需要八聚体元件第五位上有一个A,也需要与POU结构域接触。在没有POU结构域的情况下,OCA-B的一个氨基末端片段以相同的序列特异性结合八聚体位点。共激活因子OCA-B可能会发生依赖于POU的构象变化,从而暴露出其氨基末端,使其能够识别Oct-1或Oct-2结合位点大沟中的特定DNA序列。OCA-B对POU结构域和八聚体序列的识别为普遍存在的因子Oct-1对含八聚体位点基因进行差异调控提供了一种机制。