Morris James R, Petrov Dmitri A, Lee Anne M, Wu Chao-Ting
Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115, USA.
Genetics. 2004 Aug;167(4):1739-47. doi: 10.1534/genetics.104.026955.
Eukaryotic enhancers act over very long distances, yet still show remarkable specificity for their own promoter. To better understand mechanisms underlying this enhancer-promoter specificity, we used transvection to analyze enhancer choice between two promoters, one located in cis to the enhancer and the other in trans to the enhancer, at the yellow gene of Drosophila melanogaster. Previously, we demonstrated that enhancers at yellow prefer to act on the cis-linked promoter, but that mutation of core promoter elements in the cis-linked promoter releases enhancers to act in trans. Here, we address the mechanism by which these elements affect enhancer choice. We consider and explicitly test three models that are based on promoter competency, promoter pairing, and promoter identity. Through targeted gene replacement of the endogenous yellow gene, we show that competency of the cis-linked promoter is a key parameter in the cis-trans choice of an enhancer. In fact, complete replacement of the yellow promoter with both TATA-containing and TATA-less heterologous promoters maintains enhancer action in cis.
真核生物增强子的作用距离非常远,但对其自身的启动子仍表现出显著的特异性。为了更好地理解这种增强子 - 启动子特异性背后的机制,我们利用转位作用来分析果蝇黄色基因处两个启动子之间的增强子选择,其中一个启动子与增强子顺式相连,另一个与增强子反式相连。此前,我们证明黄色基因处的增强子倾向于作用于顺式连接的启动子,但顺式连接启动子中核心启动子元件的突变会使增强子转而反式作用。在这里,我们探讨这些元件影响增强子选择的机制。我们考虑并明确测试了基于启动子活性、启动子配对和启动子身份的三种模型。通过对内源黄色基因进行靶向基因替换,我们表明顺式连接启动子的活性是增强子顺反选择的关键参数。事实上,用含TATA和不含TATA的异源启动子完全替换黄色启动子后,增强子仍能顺式发挥作用。