Gutierrez Pedro A, Baughman Kirk, Sun Yadong, Tong Liang
Department of Biological Sciences, Columbia University, New York, New York 10027, USA.
RNA. 2021 Oct;27(10):1148-1154. doi: 10.1261/rna.078764.121. Epub 2021 Jul 6.
CPSF73 is the endonuclease that catalyzes the cleavage reaction for 3'-end processing of mRNA precursors (pre-mRNAs) in two distinct machineries, a canonical machinery for the majority of pre-mRNAs and a U7 snRNP (U7 machinery) for replication-dependent histone pre-mRNAs in animal cells. CPSF73 also possesses 5'-3' exonuclease activity in the U7 machinery, degrading the downstream cleavage product after the endonucleolytic cleavage. Recent studies show that CPSF73 is a potential target for developing anticancer, antimalarial, and antiprotozoal drugs, spurring interest in identifying new small-molecule inhibitors against this enzyme. CPSF73 nuclease activity has so far been demonstrated using a gel-based end-point assay, using radiolabeled or fluorescently labeled RNA substrates. By taking advantage of unique properties of the U7 machinery, we have developed a novel, real-time fluorescence assay for the nuclease activity of CPSF73. This assay is facile and high-throughput, and should also be helpful for the discovery of new CPSF73 inhibitors.
CPSF73是一种核酸内切酶,它在两种不同的机制中催化mRNA前体(前体mRNA)3'端加工的切割反应,一种是大多数前体mRNA的经典机制,另一种是动物细胞中依赖复制的组蛋白前体mRNA的U7 snRNP(U7机制)。CPSF73在U7机制中还具有5'-3'核酸外切酶活性,在内切核酸酶切割后降解下游切割产物。最近的研究表明,CPSF73是开发抗癌、抗疟疾和抗原生动物药物的潜在靶点,这激发了人们对鉴定针对该酶的新型小分子抑制剂的兴趣。到目前为止,CPSF73核酸酶活性已通过基于凝胶的终点测定法得到证实,该方法使用放射性标记或荧光标记的RNA底物。利用U7机制的独特特性,我们开发了一种用于CPSF73核酸酶活性的新型实时荧光测定法。该测定法简便且高通量,也有助于发现新的CPSF73抑制剂。