Erman B, Sen R
Rosenstiel Basic Medical Sciences Research Center and Department of Biology, Brandeis University, Waltham, MA 02254, USA.
EMBO J. 1996 Sep 2;15(17):4665-75.
Enhancers and promoters nucleate the assembly of multiprotein complexes that are required for the transcriptional activation of eukaryotic genes. Although multimerized binding sites of individual transcription factors sometimes mimic the properties of an enhancer, the combinatorial use of factors is considered to be crucial for achieving biological specificity. The minimal B cell specific immunoglobulin mu heavy chain gene enhancer is activated by a combination of tissue-restricted ETS proteins and ubiquitously expressed basic helix-loop-helix transcription factors. Here we show that a domain of PU.1 that activates transcription from multimerized PU.1 binding sites is not required to activate the mu enhancer together with Ets-1. In contrast, a transactivation domain in Ets-1 is necessary to activate this enhancer synergistically with PU.1. Furthermore, the Ets-1 activation domain functions only when tethered to the muA site of the enhancer. These observations illuminate two forms of context dependence: first, all possible transcription activation domains may not be required to achieve combinatorial specificity; second, functional transcription activation domains may require appropriate positioning on DNA.
增强子和启动子促使多蛋白复合物组装,而这些复合物是真核基因转录激活所必需的。虽然单个转录因子的多聚化结合位点有时会模拟增强子的特性,但人们认为因子的组合使用对于实现生物学特异性至关重要。最小的B细胞特异性免疫球蛋白μ重链基因增强子由组织限制性ETS蛋白和普遍表达的碱性螺旋-环-螺旋转录因子共同激活。在此我们表明,激活多聚化PU.1结合位点转录的PU.1结构域并非与Ets-1共同激活μ增强子所必需的。相反,Ets-1中的一个反式激活结构域对于与PU.1协同激活该增强子是必需的。此外,Ets-1激活结构域仅在与增强子的μA位点相连时才起作用。这些观察结果揭示了两种形式的上下文依赖性:第一,实现组合特异性可能并不需要所有可能的转录激活结构域;第二,功能性转录激活结构域可能需要在DNA上进行适当定位。