School of Molecular Sciences, The University of Western Australia, Perth, Australia.
ARNA Laboratory, IECB, INSERM U1212, CNRS UMR5320, Université de Bordeaux, Pessac, France.
Biochimie. 2021 Nov;190:124-131. doi: 10.1016/j.biochi.2021.07.008. Epub 2021 Jul 27.
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.
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。