Mutation of the gene encoding the ribonuclease P RNA in the hyperthermophilic archaeon Thermococcus kodakarensis causes decreased growth rate and impaired processing of tRNA precursors
- PMID: 26551464
- DOI: 10.1016/j.bbrc.2015.11.012
Mutation of the gene encoding the ribonuclease P RNA in the hyperthermophilic archaeon Thermococcus kodakarensis causes decreased growth rate and impaired processing of tRNA precursors
Abstract
Ribonuclease P (RNase P) catalyzes the processing of 5' leader sequences of tRNA precursors in all three phylogenetic domains. RNase P also plays an essential role in non-tRNA biogenesis in bacterial and eukaryotic cells. For archaeal RNase Ps, additional functions, however, remain poorly understood. To gain insight into the biological function of archaeal RNase Ps in vivo, we prepared archaeal mutants KUWΔP3, KUWΔP8, and KUWΔP16, in which the gene segments encoding stem-loops containing helices, respectively, P3, P8 and P16 in RNase P RNA (TkopRNA) of the hyperthermophilic archaeon Thermococcus kodakarensis were deleted. Phenotypic analysis showed that KUWΔP3 and KUWΔP16 grew slowly compared with wild-type T. kodakarensis KUW1, while KUWΔP8 displayed no difference from T. kodakarensis KUW1. RNase P isolated using an affinity-tag from KUWΔP3 had reduced pre-tRNA cleavage activity compared with that from T. kodakarensis KUW1. Moreover, quantitative RT-PCR (qRT-PCR) and Northern blots analyses of KUWΔP3 showed greater accumulation of unprocessed transcripts for pre-tRNAs than that of T. kodakarensis KUW1. The current study represents the first attempt to prepare mutant T. kodakarensis with impaired RNase P for functional investigation. Comparative whole-transcriptome analysis of T. kodakarensis KUW1 and KUWΔP3 should allow for the comprehensive identification of RNA substrates for archaeal RNase Ps.
Keywords: Hyperthermophilic archaea; Pre-tRNA processing; Ribonuclease P; Thermococcus kodakarensis.
Copyright © 2015 Elsevier Inc. All rights reserved.
Similar articles
-
On archaeal homologs of the human RNase P proteins Pop5 and Rpp30 in the hyperthermophilic archaeon Thermococcus kodakarensis.Biosci Biotechnol Biochem. 2015;79(6):952-9. doi: 10.1080/09168451.2014.1003130. Epub 2015 Feb 23. Biosci Biotechnol Biochem. 2015. PMID: 25704799
-
Distinct Modified Nucleosides in tRNATrp from the Hyperthermophilic Archaeon Thermococcus kodakarensis and Requirement of tRNA m2G10/m22G10 Methyltransferase (Archaeal Trm11) for Survival at High Temperatures.J Bacteriol. 2019 Oct 4;201(21):e00448-19. doi: 10.1128/JB.00448-19. Print 2019 Nov 1. J Bacteriol. 2019. PMID: 31405913 Free PMC article.
-
Extra-structural elements in the RNA recognition motif in archaeal Pop5 play a crucial role in the activation of RNase P RNA from Pyrococcus horikoshii OT3.Biochem Biophys Res Commun. 2013 Nov 1;440(4):594-8. doi: 10.1016/j.bbrc.2013.09.140. Epub 2013 Oct 10. Biochem Biophys Res Commun. 2013. PMID: 24120499
-
Structural basis for activation of an archaeal ribonuclease P RNA by protein cofactors.Biosci Biotechnol Biochem. 2017 Sep;81(9):1670-1680. doi: 10.1080/09168451.2017.1353404. Epub 2017 Jul 17. Biosci Biotechnol Biochem. 2017. PMID: 28715256 Review.
-
Ribonuclease P: unity and diversity in a tRNA processing ribozyme.Annu Rev Biochem. 1998;67:153-80. doi: 10.1146/annurev.biochem.67.1.153. Annu Rev Biochem. 1998. PMID: 9759486 Review.
Cited by
-
Dynamic RNA acetylation revealed by quantitative cross-evolutionary mapping.Nature. 2020 Jul;583(7817):638-643. doi: 10.1038/s41586-020-2418-2. Epub 2020 Jun 17. Nature. 2020. PMID: 32555463 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources