Temasek Life Sciences Laboratory, 1 Research Link, National University of Singapore 117604, Singapore.
School of Biological Sciences, Nanyang Technological University, 60 Nanyang Drive, Singapore 639798, Singapore.
Nucleic Acids Res. 2019 Apr 8;47(6):3101-3116. doi: 10.1093/nar/gky1300.
Argonaute proteins play important roles in gene regulation with small RNAs (sRNAs) serving as guides to targets. Argonautes are believed to bind sRNAs in a sequence non-specific manner. However, we recently discovered that Argonautes selectively load endogenous single-stranded (ss) RNAs, suggesting that Argonaute loading may conform to sequence specificity. To identify sequences preferred for Argonaute loading, we have developed HIgh-throughput Sequencing mediated Specificity Analysis (HISSA). HISSA allows massively parallel analysis of RNA binding efficiency by using randomized oligos in in vitro binding assays and quantifying RNAs by deep-sequencing. We chose Drosophila as a model system to take advantage of the presence of two biochemically distinct Argonautes, AGO1 and AGO2. Our results revealed AGO2 loading to be strongly favored by G-rich sequences. In contrast, AGO1 showed an enrichment of the 'GAC' motif in loaded species. Reanalysis of published sRNA sequencing data from fly tissues detected enrichment of the GAC motif in ssRNA-derived small RNAs in the immunopurified AGO1-complex under certain conditions, suggesting that the sequence preference of AGO1-loading may influence the repertoire of AGO1-bound endogenous sRNAs. Finally, we showed that human Ago2 also exhibited selectivity in loading ssRNAs in cell lysates. These findings may have implications for therapeutic ssRNA-mediated gene silencing.
Argonaute 蛋白在基因调控中发挥着重要作用,小 RNA(sRNA)作为靶向物的向导。Argonaute 蛋白被认为以非序列特异性的方式结合 sRNA。然而,我们最近发现 Argonaute 蛋白选择性地加载内源性单链(ss)RNA,这表明 Argonaute 蛋白的加载可能符合序列特异性。为了鉴定 Argonaute 蛋白加载的偏好序列,我们开发了高通量测序介导的特异性分析(HISSA)。HISSA 通过在体外结合实验中使用随机化寡核苷酸,并通过深度测序对 RNA 进行定量,实现了大规模平行分析 RNA 结合效率。我们选择果蝇作为模型系统,利用两种生化上不同的 Argonaute 蛋白(AGO1 和 AGO2)的存在。我们的结果表明,AGO2 的加载强烈偏好富含 G 的序列。相比之下,AGO1 在加载的物种中富集了“GAC”基序。在某些条件下,对来自果蝇组织的已发表 sRNA 测序数据的重新分析检测到免疫纯化的 AGO1 复合物中富含 GAC 基序的 ssRNA 衍生的小 RNA 的富集,这表明 AGO1 加载的序列偏好可能影响 AGO1 结合的内源性 sRNA 谱。最后,我们表明人 Ago2 也在细胞裂解物中显示出 ssRNA 加载的选择性。这些发现可能对治疗性 ssRNA 介导的基因沉默具有影响。