Distributive enzyme binding controlled by local RNA context results in 3′ to 5′ directional processing of dicistronic tRNA precursors by Escherichia coli ribonuclease P

• Published in: Nucleic acids research Vol. 47; no. 3; pp. 1451 - 1467
• Main Authors: Zhao, Jing, Harris, Michael E
• Format: Journal Article
• Language: English
• Published: England Oxford University Press 20.02.2019
• Subjects: Escherichia coli - chemistry; Escherichia coli - genetics; Lysine - chemistry; Ribonuclease P - chemistry; Ribonuclease P - genetics; RNA and RNA-protein complexes; RNA Processing, Post-Transcriptional - genetics; RNA, Transfer - genetics; RNA-Binding Motifs - genetics; Structure-Activity Relationship; Substrate Specificity; Valine - chemistry
• ISSN: 0305-1048; 1362-4962
• DOI: 10.1093/nar/gky1162

Abstract RNA processing by ribonucleases and RNA modifying enzymes often involves sequential reactions of the same enzyme on a single precursor transcript. In Escherichia coli, processing of polycistronic tRNA precursors involves separation into individual pre-tRNAs by one of several ribonucleases followed by 5′ end maturation by ribonuclease P. A notable exception are valine and lysine tRNAs encoded by three polycistronic precursors that follow a recently discovered pathway involving initial 3′ to 5′ directional processing by RNase P. Here, we show that the dicistronic precursor containing tRNAvalV and tRNAvalW undergoes accurate and efficient 3′ to 5′ directional processing by RNase P in vitro. Kinetic analyses reveal a distributive mechanism involving dissociation of the enzyme between the two cleavage steps. Directional processing is maintained despite swapping or duplicating the two tRNAs consistent with inhibition of processing by 3′ trailer sequences. Structure-function studies identify a stem–loop in 5′ leader of tRNAvalV that inhibits RNase P cleavage and further enforces directional processing. The results demonstrate that directional processing is an intrinsic property of RNase P and show how RNA sequence and structure context can modulate reaction rates in order to direct precursors along specific pathways.