Busi Florent, Arluison Véronique, Régnier Philippe
Université Paris Diderot & LLB/CEA/CNRS, Gif-sur-Yvette, France.
Unité de Biologie Fonctionnelle et Adaptative, CNRS UMR 8251, Paris, France.
Methods Mol Biol. 2018;1737:231-248. doi: 10.1007/978-1-4939-7634-8_14.
Regulation of RNA turnover is of utmost importance for controlling the concentration of transcripts and consequently cellular protein levels. Among the processes controlling RNA decay, small noncoding regulatory RNAs (sRNAs) have recently emerged as major new players. In this chapter, we describe and discuss protocols that can be used to measure sRNA concentration in vivo and to assess sRNA decay rates in Gram-negative bacteria. Precisely, we focus our analyses on the Escherichia coli Gram-negative bacterium as a model. The information described in this chapter provides a guideline to help develop a protocol in order to assess these important parameters and to identify RNA-processing enzymes involved in sRNA degradation processes.
RNA 周转的调控对于控制转录本浓度进而控制细胞蛋白质水平至关重要。在控制 RNA 降解的过程中,小型非编码调节 RNA(sRNA)最近已成为主要的新参与者。在本章中,我们描述并讨论了可用于体内测量 sRNA 浓度以及评估革兰氏阴性菌中 sRNA 降解速率的实验方案。具体而言,我们将分析重点放在以大肠杆菌这种革兰氏阴性菌作为模型上。本章所描述的信息提供了一个指导方针,以帮助制定一个实验方案,以便评估这些重要参数并鉴定参与 sRNA 降解过程的 RNA 加工酶。