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Activation of Haa1 and War1 transcription factors by differential binding of weak acid anions in Saccharomyces cerevisiae

机译:啤酒酵母中弱酸性阴离子的差异结合激活Haa1和War1转录因子

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摘要

In Saccharomyces cerevisiae, Haa1 and War1 transcription factors are involved in cellular adaptation against hydrophilic weak acids and lipophilic weak acids, respectively. However, it is unclear how these transcription factors are differentially activated depending on the identity of the weak acid. Using a field-effect transistor (FET)-type biosensor based on carbon nanofibers, in the present study we demonstrate that Haa1 and War1 directly bind to various weak acid anions with different affinities. Haa1 is most sensitive to acetate, followed by lactate, whereas War1 is most sensitive to benzoate, followed by sorbate, reflecting their differential activation during weak acid stresses. We show that DNA binding by Haa1 is induced in the presence of acetic acid and that the N-terminal Zn-binding domain is essential for this activity. Acetate binds to the N-terminal 150-residue region, and the transcriptional activation domain is located between amino acid residues 230 and 483. Our data suggest that acetate binding converts an inactive Haa1 to the active form, which is capable of DNA binding and transcriptional activation.
机译:在酿酒酵母中,Haa1和War1转录因子分别参与细胞对亲水性弱酸和亲脂性弱酸的适应。但是,尚不清楚这些转录因子如何根据弱酸的身份而被不同地激活。使用基于碳纳米纤维的场效应晶体管(FET)型生物传感器,在本研究中,我们证明了Haa1和War1直接结合具有不同亲和力的各种弱酸阴离子。 Haa1对乙酸盐最敏感,其次是乳酸盐,而War1对苯甲酸盐最敏感,其次是山梨酸盐,反映了它们在弱酸胁迫下的差异激活。我们表明由Haa1的DNA结合是在乙酸的存在下诱导的,并且N末端Zn结合结构域对该活性至关重要。乙酸盐与N末端150个残基区域结合,转录激活结构域位于氨基酸残基230和483之间。我们的数据表明,乙酸盐结合将无活性的Haa1转化为活性形式,该形式能够进行DNA结合和转录激活。

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