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在启动子区域的 G-四链体结构作为基因表达的调控元件发挥作用。

A G-Quadruplex Structure in the Promoter Region of Functions as a Regulatory Element for Gene Expression.

机构信息

Department of Biochemical Science and Technology, National Taiwan University, Taipei 106, Taiwan.

Institute of Atomic and Molecular Sciences, Academia Sinica, Taipei 115, Taiwan.

出版信息

Int J Mol Sci. 2018 Sep 10;19(9):2678. doi: 10.3390/ijms19092678.

Abstract

The differential transcriptional expression of between tumor cells and the surrounding stroma during cancer progression has been suggested to have a tumor-promoting effect. However, little is known about the transcriptional regulation of . To better understand how this gene is regulated, the promoter region of was analyzed. We found that a high GC content near the transcriptional start site (TSS) might form an alternative G-quadruplex (G4) structure. Nuclear magnetic resonance spectroscopy (NMR) confirmed their formation in vitro. The reporter assay showed that one of the G4 structures exerted a regulatory role in gene transcription. When the G4-forming sequence was mutated to disrupt the G4 structure, the transcription activity dropped. To examine whether this G4 structure actually has an influence on gene transcription in the chromosome, we utilized the CRISPR/Cas9 system to edit the G4-forming sequence within the promoter in the cell genome. The pop-in/pop-out strategy was adopted to isolate the precisely-edited A375 cell clone. In CRISPR-modified A375 cell clones whose G4 was disrupted, there was a decrease in the endogenous messenger RNA (mRNA) expression level. In conclusion, we found that the G4 structure in the promoter might play an important role in regulating the level of transcription.

摘要

在癌症进展过程中,肿瘤细胞与周围基质之间的差异转录表达被认为具有促进肿瘤的作用。然而,关于 的转录调控知之甚少。为了更好地理解这个基因是如何被调控的,我们分析了 的启动子区域。我们发现,靠近转录起始位点(TSS)的高 GC 含量可能形成一种替代的 G-四链体(G4)结构。核磁共振波谱(NMR)实验在体外证实了它们的形成。报告基因实验表明,G4 结构之一在基因转录中发挥调节作用。当 G4 形成序列发生突变以破坏 G4 结构时,转录活性下降。为了研究这种 G4 结构是否真的会影响染色体上的基因转录,我们利用 CRISPR/Cas9 系统在细胞基因组中编辑 的启动子中的 G4 形成序列。采用 pop-in/pop-out 策略分离出精确编辑的 A375 细胞克隆。在 G4 被破坏的 CRISPR 修饰的 A375 细胞克隆中,内源性 的信使 RNA(mRNA)表达水平下降。总之,我们发现 启动子中的 G4 结构可能在调节转录水平方面发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f7/6165315/eaf4b5bad067/ijms-19-02678-g001.jpg

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