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果蝇生物钟中 PER 的动态 PER 抑制机制:从 DNA 上到 DNA 外。

Dynamic PER repression mechanisms in the Drosophila circadian clock: from on-DNA to off-DNA.

机构信息

Department of Biology, Howard Hughes Medical Institute, National Center for Behavioral Genomics, Brandeis University, Waltham, Massachusetts 02454, USA.

出版信息

Genes Dev. 2010 Feb 15;24(4):358-67. doi: 10.1101/gad.1883910.

Abstract

Transcriptional feedback loops are central to the generation and maintenance of circadian rhythms. In animal systems as well as Neurospora, transcriptional repression is believed to occur by catalytic post-translational events. We report here in the Drosophila model two different mechanisms by which the circadian repressor PERIOD (PER) inhibits CLOCK/CYCLE (CLK/CYC)-mediated transcription. First, PER is recruited to circadian promoters, which leads to the nighttime decrease of CLK/CYC activity. This decrease is proportional to PER levels on DNA, and PER recruitment probably occurs via CLK. Then CLK is released from DNA and sequestered in a strong, approximately 1:1 PER-CLK off-DNA complex. The data indicate that the PER levels bound to CLK change dynamically and are important for repression, first on-DNA and then off-DNA. They also suggest that these mechanisms occur upstream of post-translational events, and that elements of this two-step mechanism likely apply to mammals.

摘要

转录反馈回路是昼夜节律产生和维持的核心。在动物系统和 Neurospora 中,转录抑制被认为是通过催化的翻译后事件发生的。我们在这里的果蝇模型中报告了两种不同的机制,即昼夜节律抑制剂 PERIOD(PER)如何抑制 CLOCK/CYCLE(CLK/CYC)介导的转录。首先,PER 被招募到昼夜节律启动子上,导致夜间 CLK/CYC 活性的降低。这种降低与 DNA 上的 PER 水平成正比,并且 PER 的招募可能通过 CLK 发生。然后 CLK 从 DNA 上释放出来,并被强的、大约 1:1 的 PER-CLK 离线 DNA 复合物隔离。数据表明,与 CLK 结合的 PER 水平动态变化,对于在 DNA 上和在 DNA 外的抑制很重要。它们还表明,这些机制发生在后翻译事件的上游,并且该两步机制的要素可能适用于哺乳动物。

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