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热休克转录因子(HSFs)与不同结合序列之间的相互作用:酵母HSFs和人类HSF1的结合特异性

Interaction between heat shock transcription factors (HSFs) and divergent binding sequences: binding specificities of yeast HSFs and human HSF1.

作者信息

Sakurai Hiroshi, Takemori Yukiko

机构信息

Division of Health Sciences, Graduate School of Medical Science, Kanazawa University, 5-11-80 Kodatsuno, Kanazawa, Ishikawa 920-0942, Japan.

出版信息

J Biol Chem. 2007 May 4;282(18):13334-41. doi: 10.1074/jbc.M611801200. Epub 2007 Mar 8.

Abstract

The target genes of the heat shock transcription factor (HSF) contain a cis-acting sequence, the heat shock element (HSE), which consists of multiple inverted repeats of the sequence 5'-nGAAn-3'. Using data acquired in this and a previous study, we have identified the HSEs in 59 of 62 target genes of Saccharomyces cerevisiae Hsf1. The Hsf1 protein recognizes continuous and discontinuous repeats of the nGAAn unit; the nucleotide sequences and configuration of the units diverge slightly among functional HSEs. When Schizosaccharomyces pombe HSF was expressed in S. cerevisiae cells, heat shock induced S. pombe HSF to bind to various HSE types, which properly activated transcription from almost all target genes, suggesting that the S. pombe genome also contains divergent HSEs. Human HSF1 induced the heat shock response via HSEs with continuous units in S. cerevisiae cells but failed to do so via HSEs with discontinuous units. Binding of human HSF1 to the discontinuous type of HSE was observed in vitro but was significantly inhibited in vivo. These results show that human HSF1 recognizes HSEs in a slightly different way than yeast HSFs and suggest that the configuration of the unit is an important determinant for HSF-HSE interactions.

摘要

热休克转录因子(HSF)的靶基因含有一个顺式作用序列,即热休克元件(HSE),它由5'-nGAAn-3'序列的多个反向重复组成。利用本研究及之前一项研究中获得的数据,我们在酿酒酵母Hsf1的62个靶基因中的59个中鉴定出了HSE。Hsf1蛋白识别nGAAn单元的连续和不连续重复;这些单元的核苷酸序列和构型在功能性HSE之间略有差异。当粟酒裂殖酵母HSF在酿酒酵母细胞中表达时,热休克诱导粟酒裂殖酵母HSF与各种类型的HSE结合,从而几乎正确激活了所有靶基因的转录,这表明粟酒裂殖酵母基因组中也含有不同的HSE。人类HSF1在酿酒酵母细胞中通过具有连续单元的HSE诱导热休克反应,但通过具有不连续单元的HSE则无法诱导。在体外观察到人类HSF1与不连续类型的HSE结合,但在体内显著受到抑制。这些结果表明,人类HSF1识别HSE的方式与酵母HSF略有不同,这表明单元的构型是HSF-HSE相互作用的一个重要决定因素。

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