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Identification and Sequence Analysis of Metazoan tRNA 3′-End Processing Enzymes tRNase Zs
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 tRNas...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3433465/ https://www.ncbi.nlm.nih.gov/pubmed/22962606 http://dx.doi.org/10.1371/journal.pone.0044264 |
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author | Wang, Zhikang Zheng, Jia Zhang, Xiaojie Peng, Jingjing Liu, Jinyu Huang, Ying |
author_facet | Wang, Zhikang Zheng, Jia Zhang, Xiaojie Peng, Jingjing Liu, Jinyu Huang, Ying |
author_sort | Wang, Zhikang |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-3433465 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34334652012-09-07 Identification and Sequence Analysis of Metazoan tRNA 3′-End Processing Enzymes tRNase Zs Wang, Zhikang Zheng, Jia Zhang, Xiaojie Peng, Jingjing Liu, Jinyu Huang, Ying PLoS One Research Article 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. Public Library of Science 2012-09-04 /pmc/articles/PMC3433465/ /pubmed/22962606 http://dx.doi.org/10.1371/journal.pone.0044264 Text en © 2012 Wang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Wang, Zhikang Zheng, Jia Zhang, Xiaojie Peng, Jingjing Liu, Jinyu Huang, Ying Identification and Sequence Analysis of Metazoan tRNA 3′-End Processing Enzymes tRNase Zs |
title | Identification and Sequence Analysis of Metazoan tRNA 3′-End Processing Enzymes tRNase Zs |
title_full | Identification and Sequence Analysis of Metazoan tRNA 3′-End Processing Enzymes tRNase Zs |
title_fullStr | Identification and Sequence Analysis of Metazoan tRNA 3′-End Processing Enzymes tRNase Zs |
title_full_unstemmed | Identification and Sequence Analysis of Metazoan tRNA 3′-End Processing Enzymes tRNase Zs |
title_short | Identification and Sequence Analysis of Metazoan tRNA 3′-End Processing Enzymes tRNase Zs |
title_sort | identification and sequence analysis of metazoan trna 3′-end processing enzymes trnase zs |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3433465/ https://www.ncbi.nlm.nih.gov/pubmed/22962606 http://dx.doi.org/10.1371/journal.pone.0044264 |
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