» Articles » PMID: 22962606

Identification and Sequence Analysis of Metazoan TRNA 3'-end Processing Enzymes TRNase Zs

Overview
Journal PLoS One
Date 2012 Sep 11
PMID 22962606
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

tRNase Z is the endonuclease responsible for removing the 3'-trailer sequences from precursor tRNAs, a prerequisite for the addition of the CCA sequence. It occurs in the short (tRNase Z(S)) and long (tRNase Z(L)) forms. Here we report the identification and sequence analysis of candidate tRNase Zs from 81 metazoan species. We found that the vast majority of deuterostomes, lophotrochozoans and lower metazoans have one tRNase Z(S) and one tRNase Z(L) genes, whereas ecdysozoans possess only a single tRNase Z(L) gene. Sequence analysis revealed that in metazoans, a single nuclear tRNase Z(L) gene is likely to encode both the nuclear and mitochondrial forms of tRNA 3'-end processing enzyme through mechanisms that include alternative translation initiation from two in-frame start codons and alternative splicing. Sequence conservation analysis revealed a variant PxKxRN motif, PxPxRG, which is located in the N-terminal region of tRNase Z(S)s. We also identified a previously unappreciated motif, AxDx, present in the C-terminal region of both tRNase Z(S)s and tRNase Z(L)s. The AxDx motif consisting mainly of a very short loop is potentially close enough to form hydrogen bonds with the loop containing the PxKxRN or PxPxRG motif. Through complementation analysis, we demonstrated the likely functional importance of the AxDx motif. In conclusion, our analysis supports the notion that in metazoans a single tRNase Z(L) has evolved to participate in both nuclear and mitochondrial tRNA 3'-end processing, whereas tRNase Z(S) may have evolved new functions. Our analysis also unveils new evolutionarily conserved motifs in tRNase Zs, including the C-terminal AxDx motif, which may have functional significance.

Citing Articles

Molecular basis of human nuclear and mitochondrial tRNA 3' processing.

Bhatta A, Kuhle B, Yu R, Spanaus L, Ditter K, Bohnsack K Nat Struct Mol Biol. 2025; .

PMID: 39747487 DOI: 10.1038/s41594-024-01445-w.


Mutations in ELAC2 associated with hypertrophic cardiomyopathy impair mitochondrial tRNA 3'-end processing.

Saoura M, Powell C, Kopajtich R, Alahmad A, Al-Balool H, Albash B Hum Mutat. 2019; 40(10):1731-1748.

PMID: 31045291 PMC: 6764886. DOI: 10.1002/humu.23777.


The mitochondrial transcriptome.

Shang J, Yang Y, Wu L, Zou M, Huang Y RNA. 2018; 24(9):1241-1254.

PMID: 29954949 PMC: 6097661. DOI: 10.1261/rna.064477.117.


The crystal structure of Trz1, the long form RNase Z from yeast.

Ma M, Li de la Sierra-Gallay I, Lazar N, Pellegrini O, Durand D, Marchfelder A Nucleic Acids Res. 2017; 45(10):6209-6216.

PMID: 28379452 PMC: 5449637. DOI: 10.1093/nar/gkx216.


Identification of glutathione (GSH)-independent glyoxalase III from Schizosaccharomyces pombe.

Zhao Q, Su Y, Wang Z, Chen C, Wu T, Huang Y BMC Evol Biol. 2014; 14:86.

PMID: 24758716 PMC: 4021431. DOI: 10.1186/1471-2148-14-86.


References
1.
Smith C, Patton J, Nadal-Ginard B . Alternative splicing in the control of gene expression. Annu Rev Genet. 1989; 23:527-77. DOI: 10.1146/annurev.ge.23.120189.002523. View

2.
Minagawa A, Takaku H, Ishii R, Takagi M, Yokoyama S, Nashimoto M . Identification by Mn2+ rescue of two residues essential for the proton transfer of tRNase Z catalysis. Nucleic Acids Res. 2006; 34(13):3811-8. PMC: 1540738. DOI: 10.1093/nar/gkl517. View

3.
Fan L, Wang Z, Liu J, Guo W, Yan J, Huang Y . A survey of green plant tRNA 3'-end processing enzyme tRNase Zs, homologs of the candidate prostate cancer susceptibility protein ELAC2. BMC Evol Biol. 2011; 11:219. PMC: 3161902. DOI: 10.1186/1471-2148-11-219. View

4.
Ho S, Hunt H, Horton R, Pullen J, Pease L . Site-directed mutagenesis by overlap extension using the polymerase chain reaction. Gene. 1989; 77(1):51-9. DOI: 10.1016/0378-1119(89)90358-2. View

5.
Schilling O, Spath B, Kostelecky B, Marchfelder A, Meyer-Klaucke W, Vogel A . Exosite modules guide substrate recognition in the ZiPD/ElaC protein family. J Biol Chem. 2005; 280(18):17857-62. DOI: 10.1074/jbc.M500591200. View