Department of Biology and Biotechnology "Charles Darwin", Sapienza University of Rome, P.le Aldo Moro 5, 00185 Rome, Italy.
Department of Biochemical Sciences, Sapienza University of Rome, P.le Aldo Moro 5, 00185 Rome, Italy.
Biomolecules. 2019 Sep 17;9(9):497. doi: 10.3390/biom9090497.
Studying transcription machinery assembly is challenging because of long intrinsically disordered regions present within the multi-modular transcription factors. One example is alcohol dehydrogenase repressor 1 (Adr1p) from fermenting yeast, responsible for the metabolic switch from glucose to ethanol. The role of each individual transcription activation domain (TAD) has been previously studied, but their interplay and their roles in enhancing the stability of the protein is not known. In this work, we designed five unique miniAdr1 constructs containing either TADs I-II-III or TAD I and III, connected by linkers of different sizes and compositions. We demonstrated that miniAdr1-BL, containing only PAR-TAD I+III with a basic linker (BL), binds the cognate DNA sequence, located in the promoter of the (alcohol dehydrogenase 2) gene, and is necessary to stabilize the heterologous expression. In fact, we found that the sequence of the linker between TAD I and III affected the solubility of free miniAdr1 proteins, as well as the stability of their complexes with DNA. miniAdr1-BL is the stable unit able to recognize , and hence it is a promising tool for future studies on nucleosomal DNA binding and transcription machinery assembly .
研究转录机器的组装具有挑战性,因为多模块化转录因子中存在长的固有无序区域。一个例子是发酵酵母中的醇脱氢酶阻遏物 1(Adr1p),它负责从葡萄糖到乙醇的代谢转换。每个单独的转录激活结构域(TAD)的作用以前已经研究过,但它们的相互作用及其在增强蛋白质稳定性方面的作用尚不清楚。在这项工作中,我们设计了五个独特的 miniAdr1 构建体,分别包含 TAD I-II-III 或 TAD I 和 III,由不同大小和组成的接头连接。我们证明,仅包含 PAR-TAD I+III 和碱性接头(BL)的 miniAdr1-BL 与位于 (醇脱氢酶 2 基因)启动子中的同源 DNA 序列结合,并且是稳定异源表达所必需的。事实上,我们发现 TAD I 和 III 之间的接头序列影响游离 miniAdr1 蛋白的溶解度以及它们与 DNA 复合物的稳定性。miniAdr1-BL 是能够识别 的稳定单元,因此它是未来研究核小体 DNA 结合和转录机器组装的有前途的工具。