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酿酒酵母Pho2与Pho4的相互作用增加了Pho4激活域的可及性。

Interaction of Saccharomyces cerevisiae Pho2 with Pho4 increases the accessibility of the activation domain of Pho4.

作者信息

Shao D, Creasy C L, Bergman L W

机构信息

Department of Microbiology and Immunology, Medical College of Pennsylvania, Philadelphia 19102, USA.

出版信息

Mol Gen Genet. 1996 Jun 12;251(3):358-64. doi: 10.1007/BF02172527.

Abstract

In Saccharomyces cerevisiae, expression of acid phosphatase, encoded by the PHO5 gene, requires two positive regulatory factors, Pho4 and Pho2 (also called Bas2 or Grf10). Using GAL4-PHO4 fusions, we demonstrate that a functional interaction between these two proteins is necessary for transcriptional activation to occur. This functional interaction between Pho4 and Pho2 is independent of the presence of the negative regulatory factor, Pho80, which also interacts with Pho4. Interestingly, truncations of Pho4 missing amino acids 252-265, which encompass the basic region of the basic helix-loop-helix (bHLH) DNA binding motif, exhibit high transcriptional activation that is independent of the Pho2 molecule. Single amino acid mutations of highly conserved residues within this area all display this Pho2-independent phenotype. A region near the C-terminus of Pho2 appears to be critical for this interaction with Pho4. A model to account for the requirement for Pho2 in Pho4-dependent transcriptional activation is proposed.

摘要

在酿酒酵母中,由PHO5基因编码的酸性磷酸酶的表达需要两种正调控因子,即Pho4和Pho2(也称为Bas2或Grf10)。通过使用GAL4-PHO4融合蛋白,我们证明这两种蛋白质之间的功能相互作用对于转录激活的发生是必需的。Pho4和Pho2之间的这种功能相互作用独立于负调控因子Pho80的存在,Pho80也与Pho4相互作用。有趣的是,缺失包含碱性螺旋-环-螺旋(bHLH)DNA结合基序碱性区域的252-265位氨基酸的Pho4截短体表现出与Pho2分子无关的高转录激活。该区域内高度保守残基的单氨基酸突变均表现出这种不依赖Pho2的表型。Pho2 C末端附近的一个区域似乎对于与Pho4的这种相互作用至关重要。我们提出了一个模型来解释Pho4依赖性转录激活中对Pho2的需求。

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