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酵母热激蛋白1转录因子对于激活单个靶基因STL1至关重要。

The yeast Hot1 transcription factor is critical for activating a single target gene, STL1.

作者信息

Bai Chen, Tesker Masha, Engelberg David

机构信息

CREATE-NUS-HUJ Cellular and Molecular Mechanisms of Inflammation Programme, National University of Singapore, Singapore 138602 Department of Microbiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117456.

Department of Biological Chemistry, Institute of Life Science, Hebrew University of Jerusalem, Jerusalem 91904, Israel.

出版信息

Mol Biol Cell. 2015 Jun 15;26(12):2357-74. doi: 10.1091/mbc.E14-12-1626. Epub 2015 Apr 22.

Abstract

Transcription factors are commonly activated by signal transduction cascades and induce expression of many genes. They therefore play critical roles in determining the cell's fate. The yeast Hog1 MAP kinase pathway is believed to control the transcription of hundreds of genes via several transcription factors. To identify the bona fide target genes of Hog1, we inducibly expressed the spontaneously active variant Hog1(D170A+F318L) in cells lacking the Hog1 activator Pbs2. This system allowed monitoring the effects of Hog1 by itself. Expression of Hog1(D170A+F318L) in pbs2∆ cells imposed induction of just 105 and suppression of only 26 transcripts by at least twofold. We looked for the Hog1-responsive element within the promoter of the most highly induced gene, STL1 (88-fold). A novel Hog1 responsive element (HoRE) was identified and shown to be the direct target of the transcription factor Hot1. Unexpectedly, we could not find this HoRE in any other yeast promoter. In addition, the only gene whose expression was abolished in hot1∆ cells was STL1. Thus Hot1 is essential for transcription of just one gene, STL1. Hot1 may represent a class of transcription factors that are essential for transcription of a very few genes or even just one.

摘要

转录因子通常由信号转导级联反应激活,并诱导许多基因的表达。因此,它们在决定细胞命运中起着关键作用。酵母Hog1丝裂原活化蛋白激酶途径被认为通过几种转录因子控制数百个基因的转录。为了鉴定Hog1真正的靶基因,我们在缺乏Hog1激活剂Pbs2的细胞中诱导表达自发活性变体Hog1(D170A+F318L)。该系统允许单独监测Hog1的作用。在pbs2∆细胞中表达Hog1(D170A+F318L)仅诱导了105个转录本,且仅抑制了26个转录本至少两倍。我们在诱导程度最高的基因STL1(88倍)的启动子内寻找Hog1反应元件。一个新的Hog1反应元件(HoRE)被鉴定出来,并被证明是转录因子Hot1的直接靶点。出乎意料的是,我们在任何其他酵母启动子中都没有找到这个HoRE。此外,在hot1∆细胞中表达被消除的唯一基因是STL1。因此,Hot1对于仅一个基因STL1的转录是必不可少的。Hot1可能代表一类对极少数基因甚至仅一个基因的转录必不可少的转录因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5494/4462951/41e02090a6fb/2357fig1.jpg

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