Wellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK.
Methods Mol Biol. 2024;2807:229-242. doi: 10.1007/978-1-0716-3862-0_16.
The identification of RNA modifications at single nucleotide resolution has become an emerging area of interest within biology and specifically among virologists seeking to ascertain how this untapped area of RNA regulation may be altered or hijacked upon viral infection. Herein, we describe a straightforward biochemical approach modified from two original published Ψ mapping protocols, BID-seq and PRAISE, to specifically identify pseudouridine modifications on mRNA transcripts from an HIV-1 infected T cell line. This protocol could readily be adapted for other viral infected cell types and additionally for populations of purified virions from infected cells.
在生物学领域,尤其是在试图确定病毒感染时这种未开发的 RNA 调控区域可能发生何种改变或被劫持的病毒学家中,实现单个核苷酸分辨率下的 RNA 修饰鉴定已经成为一个新兴的研究领域。在此,我们描述了一种源自两个原始 Ψ 图谱分析方案(BID-seq 和 PRAISE)的改良生化方法,用于专门鉴定 HIV-1 感染的 T 细胞系中转录 mRNA 上的假尿嘧啶修饰。该方案可以很容易地应用于其他病毒感染的细胞类型,并且还可以应用于从感染细胞中纯化的病毒粒子群体。