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核糖体RNA产生与成熟之间的耦合:才刚刚开始。

Coupling Between Production of Ribosomal RNA and Maturation: Just at the Beginning.

作者信息

Azouzi Chaima, Jaafar Mariam, Dez Christophe, Abou Merhi Raghida, Lesne Annick, Henras Anthony K, Gadal Olivier

机构信息

Laboratoire de Biologie Moléculaire, Cellulaire et du Développement (MCD), Centre de Biologie Intégrative (CBI), CNRS, UPS, Université de Toulouse, Toulouse, France.

Genomic Stability and Biotherapy (GSBT) Laboratory, Faculty of Sciences, Rafik Hariri Campus, Lebanese University, Beirut, Lebanon.

出版信息

Front Mol Biosci. 2021 Oct 26;8:778778. doi: 10.3389/fmolb.2021.778778. eCollection 2021.

Abstract

Ribosomal RNA (rRNA) production represents the most active transcription in the cell. Synthesis of the large rRNA precursors (35S/47S in yeast/human) is achieved by up to hundreds of RNA polymerase I (Pol I) enzymes simultaneously transcribing a single rRNA gene. In this review, we present recent advances in understanding the coupling between rRNA production and nascent rRNA folding. Mapping of the distribution of Pol I along ribosomal DNA at nucleotide resolution, using either native elongating transcript sequencing (NET-Seq) or crosslinking and analysis of cDNAs (CRAC), revealed frequent Pol I pausing, and CRAC results revealed a direct coupling between pausing and nascent RNA folding. High density of Pol I per gene imposes topological constraints that establish a defined pattern of polymerase distribution along the gene, with a persistent spacing between transcribing enzymes. RNA folding during transcription directly acts as an anti-pausing mechanism, implying that proper folding of the nascent rRNA favors elongation . Defects in co-transcriptional folding of rRNA are likely to induce Pol I pausing. We propose that premature termination of transcription, at defined positions, can control rRNA production .

摘要

核糖体RNA(rRNA)的产生是细胞中最活跃的转录过程。大型rRNA前体(酵母/人类中的35S/47S)的合成是由多达数百个RNA聚合酶I(Pol I)酶同时转录单个rRNA基因来实现的。在本综述中,我们介绍了在理解rRNA产生与新生rRNA折叠之间的耦合方面的最新进展。使用天然延伸转录本测序(NET-Seq)或cDNA交联与分析(CRAC)以核苷酸分辨率绘制Pol I沿核糖体DNA的分布图谱,揭示了Pol I频繁停顿,并且CRAC结果揭示了停顿与新生RNA折叠之间的直接耦合。每个基因中Pol I的高密度施加了拓扑限制,从而建立了沿基因的聚合酶分布的特定模式,转录酶之间存在持续的间距。转录过程中的RNA折叠直接作为一种抗停顿机制,这意味着新生rRNA的正确折叠有利于延伸。rRNA共转录折叠中的缺陷可能会诱导Pol I停顿。我们提出,在特定位置的转录过早终止可以控制rRNA的产生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a621/8575686/e914db58a8b6/fmolb-08-778778-g001.jpg

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