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m6Am RNA 修饰调控基因表达。

Regulation of Gene Expression by m6Am RNA Modification.

机构信息

Department of Biology and Biotechnology 'Charles Darwin', Sapienza University of Rome, 00165 Rome, Italy.

Department of Anatomical, Histological, Forensic & Orthopedic Sciences, Section of Histology & Medical Embryology, Sapienza University of Rome, 00165 Rome, Italy.

出版信息

Int J Mol Sci. 2023 Jan 23;24(3):2277. doi: 10.3390/ijms24032277.

Abstract

The field of RNA modification, also referred to as "epitranscriptomics," is gaining more and more interest from the scientific community. More than 160 chemical modifications have been identified in RNA molecules, but the functional significance of most of them still needs to be clarified. In this review, we discuss the role of N,2'-O-dimethyladenosine (mA) in gene expression regulation. mA is present in the first transcribed nucleotide close to the cap in many mRNAs and snRNAs in mammals and as internal modification in the snRNA U2. The writer and eraser proteins for these modifications have been recently identified and their deletions have been utilized to understand their contributions in gene expression regulation. While the role of U2 snRNA-mA in splicing regulation has been reported by different independent studies, conflicting data were found for the role of cap-associated mA in mRNA stability and translation. However, despite the open debate on the role of mA in mRNA expression, the modulation of regulators produced promising results in cancer cells. We believe that the investigation on mA will continue to yield relevant results in the future.

摘要

RNA 修饰领域,也被称为“表观转录组学”,正受到科学界越来越多的关注。在 RNA 分子中已经鉴定出超过 160 种化学修饰,但它们大多数的功能意义仍需要阐明。在这篇综述中,我们讨论了 N,2'-O-二甲基腺苷(mA)在基因表达调控中的作用。mA 存在于哺乳动物许多 mRNA 和 snRNA 的第一个转录核苷酸接近帽的位置,并且作为 snRNA U2 的内部修饰。这些修饰的写入器和擦除器蛋白最近已被鉴定出来,它们的缺失被用来了解它们在基因表达调控中的贡献。虽然 U2 snRNA-mA 在剪接调控中的作用已被不同的独立研究报道,但在帽相关 mA 在 mRNA 稳定性和翻译中的作用方面发现了相互矛盾的数据。然而,尽管 mA 在 mRNA 表达中的作用存在争议,但调节剂的调节在癌细胞中产生了有希望的结果。我们相信,对 mA 的研究将在未来继续产生相关结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8909/9916840/51e1a42f7624/ijms-24-02277-g001.jpg

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