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Genome-wide Analysis Reveals New Roles for the Activation Domains of the Saccharomyces cerevisiae Heat Shock Transcription Factor (Hsf1) during the Transient Heat Shock Response

机译:全基因组分析揭示了瞬时热休克反应过程中啤酒酵母热激转录因子(Hsf1)激活域的新作用。

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摘要

In response to elevated temperatures, cells from many organisms rapidly transcribe a number of mRNAs. In Saccharomyces cerevisiae, this protective response involves two regulatory systems: the heat shock transcription factor (Hsf1) and the Msn2 and Msn4 (Msn2/4) transcription factors. Both systems modulate the induction of specific heat shock genes. However, the contribution of Hsf1, independent of Msn2/4, is only beginning to emerge. To address this question, we constructed an msn2/4 double mutant and used microarrays to elucidate the genome-wide expression program of Hsf1. The data showed that 7.6% of the genome was heat-induced. The up-regulated genes belong to a wide range of functional categories, with a significant increase in the chaperone and metabolism genes. We then focused on the contribution of the activation domains of Hsf1 to the expression profile and extended our analysis to include msn2/4Δ strains deleted for the N-terminal or C-terminal activation domain of Hsf1. Cluster analysis of the heat-induced genes revealed activation domain-specific patterns of expression, with each cluster also showing distinct preferences for functional categories. Computational analysis of the promoters of the induced genes affected by the loss of an activation domain showed a distinct preference for positioning and topology of the Hsf1 binding site. This study provides insight into the important role that both activation domains play for the Hsf1 regulatory system to rapidly and effectively transcribe its regulon in response to heat shock.
机译:响应高温,来自许多生物的细胞会迅速转录许多mRNA。在酿酒酵母中,这种保护性反应涉及两个调节系统:热休克转录因子(Hsf1)和Msn2和Msn4(Msn2 / 4)转录因子。两种系统均调节特定热激基因的诱导。但是,与Msn2 / 4无关的Hsf1的贡献才刚刚开始出现。为了解决这个问题,我们构建了一个msn2 / 4双突变体,并使用微阵列阐明了Hsf1的全基因组表达程序。数据显示7.6%的基因组是热诱导的。上调的基因属于广泛的功能类别,伴随着伴侣和代谢基因的显着增加。然后,我们集中研究了Hsf1激活域对表达谱的贡献,并扩展了我们的分析范围,包括针对Hsf1的N端或C端激活域缺失的msn2 /4Δ菌株。热诱导基因的聚类分析显示了激活域特定的表达模式,每个聚类也显示出功能类别的独特偏好。对受激活结构域丢失影响的诱导基因启动子的计算分析表明,其对Hsf1结合位点的定位和拓扑有明显的偏爱。这项研究提供了对两个激活域在Hsf1调节系统快速有效地转录其调节子以响应热冲击中发挥重要作用的见解。

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  • 年(卷),期 -1(281),43
  • 年度 -1
  • 页码 32909–32921
  • 总页数 22
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