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G-四链体 DNA 在癌症中形成核旁斑点的作用。

The role of G-Quadruplex DNA in Paraspeckle formation in cancer.

机构信息

School of Molecular Sciences, The University of Western Australia, Perth, Australia.

ARNA Laboratory, IECB, INSERM U1212, CNRS UMR5320, Université de Bordeaux, Pessac, France.

出版信息

Biochimie. 2021 Nov;190:124-131. doi: 10.1016/j.biochi.2021.07.008. Epub 2021 Jul 27.

Abstract

Paraspeckles are RNA-protein structures within the nucleus of mammalian cells, capable of orchestrating various biochemical processes. An overexpression of the architectural component of paraspeckles, a long non-coding RNA called NEAT1 (Nuclear Enriched Abundant Transcript 1), has been linked to a variety of cancers and is often associated with poor patient prognosis. Thus, there is an accumulating interest in the role of paraspeckles in carcinogenesis, however there is a limited understanding of how NEAT1 expression is regulated. Here, we demonstrate that both nuclear G-quadruplex (G4) and paraspeckle formation are significantly increased in a human breast cancer cell line compared to non-tumorigenic breast cells. Moreover, we identified and characterized G4-forming sequences within the NEAT1 promoter and demonstrate stabilization of G4 DNA with a G4-stabilizing small molecule results in a significant alteration in both paraspeckle formation and NEAT1 expression. This G4-mediated alteration of NEAT1 at both the transcriptional and post-transcriptional levels was evident in U2OS osteosarcoma cells, MCF-7 breast adenocarcinoma and MDA-MB-231 triple negative breast cancer cells.

摘要

核内多泡体是哺乳动物细胞核内的 RNA-蛋白质结构,能够协调各种生化过程。核内多泡体的结构成分,一种称为 NEAT1(核丰富的大量转录物 1)的长非编码 RNA 的过表达与多种癌症有关,并且通常与患者预后不良相关。因此,人们对核内多泡体在致癌作用中的作用越来越感兴趣,但是对于 NEAT1 表达如何受到调节的理解有限。在这里,我们证明与非致瘤性乳腺细胞相比,人乳腺癌细胞系中的核 G-四链体 (G4) 和核内多泡体的形成显著增加。此外,我们鉴定并表征了 NEAT1 启动子中的 G4 形成序列,并证明 G4 稳定小分子稳定 G4 DNA 会导致核内多泡体形成和 NEAT1 表达的显著改变。在 U2OS 骨肉瘤细胞、MCF-7 乳腺癌腺癌和 MDA-MB-231 三阴性乳腺癌细胞中,都可以明显观察到 G4 介导的 NEAT1 在转录和转录后水平上的改变。

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