Topalidou Irini, Thireos George
Institute of Molecular Biology and Biotechnology, Foundation for Research and Technology Hellas, PO Box 1527, Heraklion 711 10, Crete, Greece.
EMBO Rep. 2003 Sep;4(9):872-6. doi: 10.1038/sj.embor.embor931.
Eukaryotic transcriptional activators usually recognize short DNA motifs, which are not only located within promoter regions, but also scattered throughout the genome. Assuming that the function of activators at non-promoter regions is wasteful and perhaps harmful, one can ask whether such binding is somehow prevented or if transcription is blocked at a downstream step. Here, we show that the yeast transcriptional activator Gcn4 is associated in vivo with several non-promoter euchromatic sites. This association results in the recruitment of the SAGA (Spt3/Ada/Gcn5/acetyltransferase) complex and the consequent activity of the Gcn5 histone acetyltransferase. The functional recruitment of the Swi/Snf nucleosome-remodelling complex was also evident at sites located in positioned nucleosomes. We show that this assemblage of coactivator complexes is not productive because of the absence of core promoter elements, other than the TATA box, that are required for stable mediator recruitment.
真核转录激活因子通常识别短的DNA基序,这些基序不仅位于启动子区域,还散布于整个基因组中。假设激活因子在非启动子区域的功能是浪费的甚至可能是有害的,那么人们可能会问,这种结合是否以某种方式被阻止,或者转录是否在下游步骤被阻断。在这里,我们表明酵母转录激活因子Gcn4在体内与几个非启动子常染色质位点相关联。这种关联导致SAGA(Spt3/Ada/Gcn5/乙酰转移酶)复合物的募集以及随后Gcn5组蛋白乙酰转移酶的活性。Swi/Snf核小体重塑复合物的功能性募集在定位核小体中的位点也很明显。我们表明,由于缺乏除TATA框之外稳定中介物募集所需的核心启动子元件,这种共激活复合物的组装是无效的。