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单个核心启动子元件对转录动力学的差异上下文特异性影响。

Differential context-specific impact of individual core promoter elements on transcriptional dynamics.

作者信息

Hendy Oliver, Campbell John, Weissman Jocelyn D, Larson Daniel R, Singer Dinah S

机构信息

Experimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.

Laboratory of Receptor Biology and Gene Expression, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.

出版信息

Mol Biol Cell. 2017 Nov 7;28(23):3360-3370. doi: 10.1091/mbc.E17-06-0408. Epub 2017 Sep 20.

Abstract

Eukaryotic transcription occurs in bursts that vary in size and frequency, but the contribution of individual core promoter elements to transcriptional bursting is not known. Here we analyze the relative contributions to bursting of the individual core promoter elements-CCAAT, TATAA-like, Sp1BS, and Inr-of an MHC class I gene in primary B-cells during both basal and activated transcription. The TATAA-like, Sp1BS, and Inr elements all function as negative regulators of transcription, and each was found to contribute differentially to the overall bursting pattern of the promoter during basal transcription. Whereas the Sp1BS element regulates burst size, the Inr element regulates burst frequency. The TATAA-like element contributes to both. Surprisingly, each element has a distinct role in bursting during transcriptional activation by γ-interferon. The CCAAT element does not contribute significantly to the constitutive transcriptional dynamics of primary B-cells, but modulates both burst size and frequency in response to γ-interferon activation. The ability of core promoter elements to modulate transcriptional bursting individually allows combinatorial fine-tuning of the level of MHC class I gene expression in response to intrinsic and extrinsic signals.

摘要

真核生物转录以大小和频率各异的爆发形式发生,但单个核心启动子元件对转录爆发的贡献尚不清楚。在此,我们分析了在基础转录和激活转录过程中,初级B细胞中MHC I类基因的单个核心启动子元件——CCAAT、TATA样、Sp1结合位点(Sp1BS)和起始子(Inr)——对转录爆发的相对贡献。TATA样、Sp1BS和Inr元件均作为转录的负调控因子,并且发现在基础转录过程中,它们各自对启动子的整体爆发模式有不同贡献。Sp1BS元件调节爆发大小,而Inr元件调节爆发频率。TATA样元件对两者均有作用。令人惊讶的是,在γ干扰素介导的转录激活过程中,每个元件在爆发中都有独特作用。CCAAT元件对初级B细胞的组成型转录动态没有显著贡献,但在γ干扰素激活时调节爆发大小和频率。核心启动子元件能够单独调节转录爆发,这使得MHC I类基因表达水平能够根据内在和外在信号进行组合微调。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7c5/5687036/eb69cc12c81e/3360fig1.jpg

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