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Hot1转录因子的C末端区域与其靶基因启动子中的GGGACAAA相关序列结合。

The C-terminal region of the Hot1 transcription factor binds GGGACAAA-related sequences in the promoter of its target genes.

作者信息

Gomar-Alba Mercè, Amaral Catarina, Artacho Alejandro, D'Auria Giuseppe, Pimentel Catarina, Rodrigues-Pousada Claudina, lí del Olmo Marcel

机构信息

Departament de Bioquímica i Biologia Molecular, Facultat de Ciències Biològiques, Universitat de València, Burjassot, Valencia, Spain.

Genomics and Stress Laboratory, Instituto de Tecnologia Química e Biológica António Xavier, Universidade Nova de Lisboa, Oeiras, Portugal.

出版信息

Biochim Biophys Acta. 2015 Dec;1849(12):1385-97. doi: 10.1016/j.bbagrm.2015.10.007. Epub 2015 Nov 3.

Abstract

Response to hyperosmotic stress in the yeast Saccharomyces cerevisiae involves the participation of the general stress response mediated by Msn2/4 transcription factors and the HOG pathway. One of the transcription factors activated through this pathway is Hot1, which contributes to the control of the expression of several genes involved in glycerol synthesis and flux, or in other functions related to adaptation to adverse conditions. This work provides new data about the interaction mechanism of this transcription factor with DNA. By means of one-hybrid and electrophoretic mobility assays, we demonstrate that the C-terminal region, which corresponds to amino acids 610-719, is the DNA-binding domain of Hot1. We also describe how this domain recognizes sequence 5'-GGGACAAA-3' located in the promoter of gene STL1. The bioinformatics analysis carried out in this work allowed the identification of identical or similar sequences (with up to two mismatches) in the promoter of other Hot1 targets, where central element GGACA was quite conserved among them. Finally, we found that small variations in the sequence recognized by Hot1 may influence its ability to recognize its targets in vivo.

摘要

酿酒酵母对高渗胁迫的应答涉及由Msn2/4转录因子介导的一般应激反应和HOG途径的参与。通过该途径激活的转录因子之一是Hot1,它有助于控制参与甘油合成和通量或与适应不利条件相关的其他功能的几个基因的表达。这项工作提供了关于该转录因子与DNA相互作用机制的新数据。通过单杂交和电泳迁移率测定,我们证明对应于氨基酸610 - 719的C末端区域是Hot1的DNA结合结构域。我们还描述了该结构域如何识别位于基因STL1启动子中的序列5'-GGGACAAA-3'。在这项工作中进行的生物信息学分析使得能够在其他Hot1靶标的启动子中鉴定出相同或相似的序列(最多有两个错配),其中中心元件GGACA在它们之间相当保守。最后,我们发现Hot1识别的序列中的小变化可能会影响其在体内识别靶标的能力。

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