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CDF-1 mediated repression of cell cycle genes targets a specific subset of transactivators.

机译:CDF-1介导的细胞周期基因阻遏作用靶向反式激活子的特定子集。

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摘要

The cdc25C, cyclin A and cdc2 genes are regulated during the cell cycle through two contiguous repressor binding sites, the CDE and CHR, located in the region of transcription initiation and interacting with a factor termed CDF-1. The target of this repression seems to be transcriptional activation of these promoters by transcription factors bound upstream. The majority of these factors falls into the class of glutamine-rich activators, suggesting that CDF-1-mediated repression might be activation domain specific. In the present study we have used chimeric promoter constructs to demonstrate that the cdc25C UAS, but not the core promoter, is crucial for repression. In addition, we show that only specific transcription factors and activation domains are responsive to CDE-CHR-mediated cell cycle regulation. These observations clearly indicate that CDF-1 interferes with activation of transcription by a specific subset of transactivators. The repressible activation domains belong to the same class of glutamine-rich activators, pointing to specific interactions of CDF-1 with components of the transcription machinery. In agreement with this conclusion we find that a simple inversion of the CDF-CHR module completely abrogates cell cycle-regulated repression.
机译:cdc25C,cyclin A和cdc2基因在细胞周期中通过两个连续的阻遏物结合位点CDE和CHR进行调节,这些位点位于转录起始区域并与称为CDF-1的因子相互作用。该抑制的目标似乎是通过结合在上游的转录因子对这些启动子的转录激活。这些因素大多数属于富含谷氨酰胺的激活剂,这表明CDF-1介导的抑制可能是激活域特异性的。在本研究中,我们已使用嵌合启动子构建体来证明cdc25C UAS(而非核心启动子)对于阻遏至关重要。此外,我们表明,只有特定的转录因子和激活域才响应CDE-CHR介导的细胞周期调控。这些观察结果清楚地表明,CDF-1会干扰反式激活子的特定子集的转录激活。可抑制的激活域属于同一类富含谷氨酰胺的激活剂,表明CDF-1与转录机制的成分之间存在特定的相互作用。与此结论相符,我们发现CDF-CHR模块的简单倒置完全消除了细胞周期调节的阻遏作用。

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