Department of Pharmacology, Weill Cornell Medicine, Cornell University, New York, New York 10065, USA.
Imperial College Centre for Synthetic Biology, Imperial College London, London SW7 2AZ, United Kingdom.
RNA. 2024 Oct 16;30(11):1529-1540. doi: 10.1261/rna.080008.124.
Internal ribosomal entry sites (IRESs) recruit the ribosome to promote translation, typically in an m7G cap-independent manner. Although IRESs are well-documented in viral genomes, they have also been reported in mammalian transcriptomes, where they have been proposed to mediate cap-independent translation of mRNAs. However, subsequent studies have challenged the idea of these "cellular" IRESs. Current methods for screening and discovering IRES activity rely on a bicistronic reporter assay, which is prone to producing false positive signals if the putative IRES sequence has a cryptic promoter or cryptic splicing sites. Here, we report an assay for screening IRES activity using a genetically encoded circular RNA comprising a split nanoluciferase (nLuc) reporter. The circular split nLuc reporter is less susceptible to the various sources of false positives that adversely affect the bicistronic IRES reporter assay and provides a streamlined method for screening IRES activity. Using the circular split nLuc reporter, we find that nine reported cellular IRESs have minimal IRES activity. Overall, the circular split nLuc reporter offers a simplified approach for identifying and validating IRESs and exhibits reduced propensity for producing the types of false positives that can occur with the bicistronic reporter assay.
内部核糖体进入位点 (IRES) 招募核糖体以促进翻译,通常以 m7G 帽非依赖性方式进行。尽管 IRES 在病毒基因组中已有详细记录,但它们也在哺乳动物转录组中被报道,在那里它们被提议介导 mRNA 的帽非依赖性翻译。然而,随后的研究对这些“细胞”IRES 的想法提出了挑战。目前用于筛选和发现 IRES 活性的方法依赖于双顺反子报告基因检测,而如果假定的 IRES 序列具有隐藏的启动子或隐藏的剪接位点,则该方法容易产生假阳性信号。在这里,我们报告了一种使用包含分裂纳米荧光素酶 (nLuc) 报告基因的遗传编码环状 RNA 筛选 IRES 活性的方法。环状分裂 nLuc 报告基因不太容易受到各种假阳性信号的影响,这些假阳性信号会对双顺反子 IRES 报告基因检测产生不利影响,并且提供了一种简化的筛选 IRES 活性的方法。使用环状分裂 nLuc 报告基因,我们发现九个报道的细胞 IRES 具有最小的 IRES 活性。总体而言,环状分裂 nLuc 报告基因为识别和验证 IRES 提供了一种简化的方法,并且与双顺反子报告基因检测相比,产生假阳性的倾向降低。