揭示与调控元件相关的非编码 RNA 的功能和机制。

IF 2.6 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Biochimica et Biophysica Acta-Gene Regulatory Mechanisms Pub Date : 2024-09-01 DOI:10.1016/j.bbagrm.2024.195059
Olivier Fosseprez, Olivier Cuvier
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引用次数: 0

摘要

在过去十年中,由 RNA Pol II 产生的调控性非编码 RNA(ncRNA)被发现在各种基本细胞功能中发挥着重要作用。特别是,数以千计的 ncRNA 在增强子和启动子等转录调控元件上产生,它们可能发挥多种功能,调控正常发育、细胞编程、转录或基因组稳定性。在这里,我们回顾了涉及这些与调控元件相关的 ncRNA,特别是增强子 RNA(eRNA)和 PROMoter uPstream Transcripts(PROMPT)的机制。我们介绍了这些短寿命 RNA 的处理和降解机制。我们总结了最近的研究发现,这些发现解释了 ncRNA 如何在启动子和增强子局部或更远的地方发挥作用,或者在 RNA Pol II 产生后不久发挥作用,或者通过转录后稳定发挥作用。这些发现为 ncRNA 如何通过作用于转录和染色质结构来影响细胞命运提供了一个统一的模型,该模型可能进一步涉及参与三维核组织的各种因素。
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Uncovering the functions and mechanisms of regulatory elements-associated non-coding RNAs

Over the past decade, regulatory non-coding RNAs (ncRNAs) produced by RNA Pol II have been revealed as meaningful players in various essential cellular functions. In particular, thousands of ncRNAs are produced at transcriptional regulatory elements such as enhancers and promoters, where they may exert multiple functions to regulate proper development, cellular programming, transcription or genomic stability. Here, we review the mechanisms involving these regulatory element-associated ncRNAs, and particularly enhancer RNAs (eRNAs) and PROMoter uPstream Transcripts (PROMPTs). We contextualize the mechanisms described to the processing and degradation of these short lived RNAs. We summarize recent findings explaining how ncRNAs operate locally at promoters and enhancers, or further away, either shortly after their production by RNA Pol II, or through post-transcriptional stabilization. Such discoveries lead to a converging model accounting for how ncRNAs influence cellular fate, by acting on transcription and chromatin structure, which may further involve factors participating to 3D nuclear organization.

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来源期刊
CiteScore
9.20
自引率
2.10%
发文量
63
审稿时长
44 days
期刊介绍: BBA Gene Regulatory Mechanisms includes reports that describe novel insights into mechanisms of transcriptional, post-transcriptional and translational gene regulation. Special emphasis is placed on papers that identify epigenetic mechanisms of gene regulation, including chromatin, modification, and remodeling. This section also encompasses mechanistic studies of regulatory proteins and protein complexes; regulatory or mechanistic aspects of RNA processing; regulation of expression by small RNAs; genomic analysis of gene expression patterns; and modeling of gene regulatory pathways. Papers describing gene promoters, enhancers, silencers or other regulatory DNA regions must incorporate significant functions studies.
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