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莱茵衣藻 E 盒元件的多重角色和互作因子。

Multiple roles and interaction factors of an E-box element in Chlamydomonas reinhardtii.

机构信息

Institute of General Botany and Plant Physiology, Friedrich Schiller University, 07743 Jena, Germany.

出版信息

Plant Physiol. 2010 Apr;152(4):2243-57. doi: 10.1104/pp.109.149195. Epub 2010 Feb 12.

Abstract

The two subunits of the circadian RNA-binding protein CHLAMY1 from Chlamydomonas reinhardtii are involved in maintaining period (C1 subunit) and phase (C3 subunit) of the circadian clock. C1 coregulates the level of C3. Overexpression of C1 causes a parallel increase in C3. Both subunits can also integrate temperature information, resulting in hyperphosphorylation of C1 and up-regulation of C3 at low temperature. Temperature-dependent up-regulation of C3 is mediated predominantly by an E-box element and only partially by two DREB1A-boxes that are situated within the C3 promoter. The E-box element is also involved in circadian C3 expression. Here, we show that the C3 promoter region drives C3 coregulation by C1. We also found that replacement of the E-box prevents the coregulation of C3 in strains overexpressing C1. In contrast, replacement of any of the two DREB1A-boxes does not influence either the coregulation of C3 by increased levels of C1 or circadian C3 expression. Thus, the E-box has multiple key roles, including temperature-dependent up-regulation of C3, its circadian expression, and its coregulation by C1. Using mobility shift assays and DNA-affinity chromatography along with mass spectrometry, we characterized proteins binding specifically to the E-box region and identified five of them. By immunoblotting, we could further show that C3 that was detected in nuclear extracts can be found in the E-box-binding protein complex. Our data indicate a complex transcriptional mechanism of C3 up-regulation and a positive feedback of C3 on its own promoter region.

摘要

莱茵衣藻昼夜节律 RNA 结合蛋白 CHLAMY1 的两个亚基参与维持生物钟的周期(C1 亚基)和相位(C3 亚基)。C1 核心调控 C3 的水平。C1 的过表达导致 C3 的平行增加。两个亚基还可以整合温度信息,导致 C1 高度磷酸化和 C3 在低温下的上调。C3 的温度依赖性上调主要由 E 盒元件介导,仅部分由位于 C3 启动子内的两个 DREB1A 盒介导。E 盒元件也参与昼夜节律 C3 的表达。在这里,我们表明 C3 启动子区域通过 C1 驱动 C3 的共调控。我们还发现,替换 E 盒会阻止 C1 过表达菌株中 C3 的共调控。相比之下,替换任何两个 DREB1A 盒都不会影响 C1 水平升高对 C3 的共调控或昼夜节律 C3 的表达。因此,E 盒具有多种关键作用,包括 C3 的温度依赖性上调、昼夜节律表达及其与 C1 的共调控。通过迁移率变动分析和 DNA 亲和层析以及质谱分析,我们鉴定了特异性结合 E 盒区域的蛋白质,并鉴定了其中的五个。通过免疫印迹,我们还可以进一步表明,在核提取物中检测到的 C3 可以在 E 盒结合蛋白复合物中找到。我们的数据表明 C3 上调的转录机制复杂,并且 C3 对其自身启动子区域有正反馈。

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