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酿酒酵母减数分裂的诱导取决于转录抑制因子Ume6通过与转录激活因子Ime1的调控结合而转变为正调控因子。

Induction of meiosis in Saccharomyces cerevisiae depends on conversion of the transcriptional represssor Ume6 to a positive regulator by its regulated association with the transcriptional activator Ime1.

作者信息

Rubin-Bejerano I, Mandel S, Robzyk K, Kassir Y

机构信息

Faculty of Biology, Technion-Israel Institute of Technology, Haifa, Israel.

出版信息

Mol Cell Biol. 1996 May;16(5):2518-26. doi: 10.1128/MCB.16.5.2518.

Abstract

The transcription of meiosis-specific genes, as well as the initiation of meiosis, in the budding yeast Saccharomyces cerevisiae depends on IME1. IME1 encodes a transcriptional activator which lacks known DNA binding motifs. In this study we have determined the mode by which Ime1 specifically activates the transcription of meiotic genes. We demonstrate that Ime1 is recruited to the promoters of meiotic genes by interacting with a DNA-binding protein, Ume6. This association between Ime1 and Ume6 depends on both starvation and the activity of a protein kinase, encoded by RIM11 In the absence of Ime1, Ume6 represses the transcription of meiotic genes. However, in the presence of Ime1, or when Ume6 is fused in frame to the Gal4 activation domain, Ume6 is converted from a repressor to an activator, resulting in the transcription of meiosis-specific genes and the formation of asci.

摘要

在芽殖酵母酿酒酵母中,减数分裂特异性基因的转录以及减数分裂的起始都依赖于IME1。IME1编码一种缺乏已知DNA结合基序的转录激活因子。在本研究中,我们确定了Ime1特异性激活减数分裂基因转录的方式。我们证明,Ime1通过与一种DNA结合蛋白Ume6相互作用,被招募到减数分裂基因的启动子区域。Ime1与Ume6之间的这种关联既依赖于饥饿状态,也依赖于由RIM11编码的一种蛋白激酶的活性。在没有Ime1的情况下,Ume6会抑制减数分裂基因的转录。然而,在有Ime1存在时,或者当Ume6与Gal4激活结构域进行读码框融合时,Ume6会从一个阻遏物转变为激活因子,从而导致减数分裂特异性基因的转录以及子囊的形成。

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