Blaiseau P L, Thomas D
Centre de Génétique Moléculaire, Centre National de la Recherche Scientifique, 91198 Gif-sur-Yvette, France.
EMBO J. 1998 Nov 2;17(21):6327-36. doi: 10.1093/emboj/17.21.6327.
The transcriptional regulation of the sulfur amino acid pathway in Saccharomyces cerevisiae depends on a single activator, Met4p, whose function requires different combinations of the auxiliary factors Cbf1p, Met28p, Met31p and Met32p. The first description of how these factors cooperate to activate transcription was provided by the identification of the Cbf1-Met4-Met28 complex which is assembled on the regulatory region of the MET16 gene. In this paper, we demonstrate that other pathways are used to recruit Met4p on the 5' upstream region of the two genes, MET3 and MET28. In these cases, Met4p is tethered to DNA through two alternative complexes associating Met4p with Met28p and either Met31p or Met32p. These complexes are formed over the AAACTGTG sequence, a cis-acting element found upstream of several MET genes. The identification of a domain within Met4p that mediates its interaction with Met31p and Met32p allowed in vivo analysis of the specificity of the Met4p-containing complexes. The results therefore demonstrate that the co-regulation of a single gene network may be gained through different molecular mechanisms. In addition the sulfur system exacerbates the structural variety of the nucleoprotein complexes in which a single bZIP factor can be engaged.
酿酒酵母中硫氨基酸途径的转录调控依赖于单一激活因子Met4p,其功能需要辅助因子Cbf1p、Met28p、Met31p和Met32p的不同组合。通过鉴定在MET16基因调控区域组装的Cbf1-Met4-Met28复合物,首次描述了这些因子如何协同激活转录。在本文中,我们证明了其他途径可用于在MET3和MET28这两个基因的5'上游区域募集Met4p。在这些情况下,Met4p通过将Met4p与Met28p以及Met31p或Met32p相关联的两种替代复合物与DNA相连。这些复合物在AAACTGTG序列上形成,该序列是在几个MET基因上游发现的顺式作用元件。对Met4p内介导其与Met31p和Met32p相互作用的结构域的鉴定,使得能够在体内分析含Met4p复合物的特异性。因此,结果表明,单一基因网络的协同调控可能通过不同的分子机制实现。此外,硫系统加剧了核蛋白复合物的结构多样性,其中单个bZIP因子可能参与其中。