| Literature DB >> 30414965 |
Tien-Hao Chen1, Marcos Sotomayor2, Venkat Gopalan3.
Abstract
RNase P catalyzes removal of the 5' leader from precursor tRNAs (pre-tRNAs) in all three domains of life. Some eukaryotic cells contain multiple forms of the protein-only RNase P (PRORP) variant, prompting efforts to unravel this seeming redundancy. Previous studies concluded that there were only modest differences in the processing of typical pre-tRNAs by the three isoforms in Arabidopsis thaliana [AtPRORP1 (organellar), AtPRORP2 and AtPRORP3 (nuclear)]. Here, we investigated if different physical attributes of the three isoforms might engender payoffs under specific conditions. Our temperature-activity profiling studies revealed that AtPRORPs display substrate-identity dependent behavior at elevated temperatures (37-45 °C), with the organellar variant outperforming the nuclear counterparts. Echoing these findings, molecular dynamics simulations revealed that AtPRORP2 relative to AtPRORP1 samples a wider conformational ensemble that deviates from the crystal structure. Results from our biochemical studies and molecular dynamics simulations support the idea that AtPRORPs have overlapping but not necessarily redundant attributes and inspire new perspectives on the suitability of each variant to perform its function(s) in a specific cellular locale.Entities:
Keywords: PRORP; molecular dynamics; substrate recognition; tRNA maturation; temperature–activity profiles
Mesh:
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Year: 2018 PMID: 30414965 PMCID: PMC6349523 DOI: 10.1016/j.jmb.2018.11.004
Source DB: PubMed Journal: J Mol Biol ISSN: 0022-2836 Impact factor: 5.469