Cargando…
An evolutionary ‘intermediate state’ of mitochondrial translation systems found in Trichinella species of parasitic nematodes: co-evolution of tRNA and EF-Tu
EF-Tu delivers aminoacyl-tRNAs to ribosomes in the translation system. However, unusual truncations found in some animal mitochondrial tRNAs seem to prevent recognition by a canonical EF-Tu. We showed previously that the chromadorean nematode has two distinct EF-Tus, one of which (EF-Tu1) binds only...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2006
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1636415/ https://www.ncbi.nlm.nih.gov/pubmed/17012285 http://dx.doi.org/10.1093/nar/gkl526 |
_version_ | 1782130743781097472 |
---|---|
author | Arita, Masashi Suematsu, Takuma Osanai, Arihiro Inaba, Takashi Kamiya, Haruo Kita, Kiyoshi Sisido, Masahiko Watanabe, Yoh-ichi Ohtsuki, Takashi |
author_facet | Arita, Masashi Suematsu, Takuma Osanai, Arihiro Inaba, Takashi Kamiya, Haruo Kita, Kiyoshi Sisido, Masahiko Watanabe, Yoh-ichi Ohtsuki, Takashi |
author_sort | Arita, Masashi |
collection | PubMed |
description | EF-Tu delivers aminoacyl-tRNAs to ribosomes in the translation system. However, unusual truncations found in some animal mitochondrial tRNAs seem to prevent recognition by a canonical EF-Tu. We showed previously that the chromadorean nematode has two distinct EF-Tus, one of which (EF-Tu1) binds only to T-armless aminoacyl-tRNAs and the other (EF-Tu2) binds to D-armless Ser-tRNAs. Neither of the EF-Tus can bind to canonical cloverleaf tRNAs. In this study, by analyzing the translation system of enoplean nematode Trichinella species, we address how EF-Tus and tRNAs have evolved from the canonical structures toward those of the chromadorean translation system. Trichinella mitochondria possess three types of tRNAs: cloverleaf tRNAs, which do not exist in chromadorean nematode mitochondria; T-armless tRNAs; and D-armless tRNAs. We found two mitochondrial EF-Tu species, EF-Tu1 and EF-Tu2, in Trichinella britovi. T.britovi EF-Tu2 could bind to only D-armless Ser-tRNA, as Caenorhabditis elegans EF-Tu2 does. In contrast to the case of C.elegans EF-Tu1, however, T.britovi EF-Tu1 bound to all three types of tRNA present in Trichinella mitochondria. These results suggest that Trichinella mitochondrial translation system, and particularly the tRNA-binding specificity of EF-Tu1, could be an intermediate state between the canonical system and the chromadorean nematode mitochondrial system. |
format | Text |
id | pubmed-1636415 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-16364152006-11-29 An evolutionary ‘intermediate state’ of mitochondrial translation systems found in Trichinella species of parasitic nematodes: co-evolution of tRNA and EF-Tu Arita, Masashi Suematsu, Takuma Osanai, Arihiro Inaba, Takashi Kamiya, Haruo Kita, Kiyoshi Sisido, Masahiko Watanabe, Yoh-ichi Ohtsuki, Takashi Nucleic Acids Res RNA EF-Tu delivers aminoacyl-tRNAs to ribosomes in the translation system. However, unusual truncations found in some animal mitochondrial tRNAs seem to prevent recognition by a canonical EF-Tu. We showed previously that the chromadorean nematode has two distinct EF-Tus, one of which (EF-Tu1) binds only to T-armless aminoacyl-tRNAs and the other (EF-Tu2) binds to D-armless Ser-tRNAs. Neither of the EF-Tus can bind to canonical cloverleaf tRNAs. In this study, by analyzing the translation system of enoplean nematode Trichinella species, we address how EF-Tus and tRNAs have evolved from the canonical structures toward those of the chromadorean translation system. Trichinella mitochondria possess three types of tRNAs: cloverleaf tRNAs, which do not exist in chromadorean nematode mitochondria; T-armless tRNAs; and D-armless tRNAs. We found two mitochondrial EF-Tu species, EF-Tu1 and EF-Tu2, in Trichinella britovi. T.britovi EF-Tu2 could bind to only D-armless Ser-tRNA, as Caenorhabditis elegans EF-Tu2 does. In contrast to the case of C.elegans EF-Tu1, however, T.britovi EF-Tu1 bound to all three types of tRNA present in Trichinella mitochondria. These results suggest that Trichinella mitochondrial translation system, and particularly the tRNA-binding specificity of EF-Tu1, could be an intermediate state between the canonical system and the chromadorean nematode mitochondrial system. Oxford University Press 2006-10 2006-09-29 /pmc/articles/PMC1636415/ /pubmed/17012285 http://dx.doi.org/10.1093/nar/gkl526 Text en © 2006 The Author(s) |
spellingShingle | RNA Arita, Masashi Suematsu, Takuma Osanai, Arihiro Inaba, Takashi Kamiya, Haruo Kita, Kiyoshi Sisido, Masahiko Watanabe, Yoh-ichi Ohtsuki, Takashi An evolutionary ‘intermediate state’ of mitochondrial translation systems found in Trichinella species of parasitic nematodes: co-evolution of tRNA and EF-Tu |
title | An evolutionary ‘intermediate state’ of mitochondrial translation systems found in Trichinella species of parasitic nematodes: co-evolution of tRNA and EF-Tu |
title_full | An evolutionary ‘intermediate state’ of mitochondrial translation systems found in Trichinella species of parasitic nematodes: co-evolution of tRNA and EF-Tu |
title_fullStr | An evolutionary ‘intermediate state’ of mitochondrial translation systems found in Trichinella species of parasitic nematodes: co-evolution of tRNA and EF-Tu |
title_full_unstemmed | An evolutionary ‘intermediate state’ of mitochondrial translation systems found in Trichinella species of parasitic nematodes: co-evolution of tRNA and EF-Tu |
title_short | An evolutionary ‘intermediate state’ of mitochondrial translation systems found in Trichinella species of parasitic nematodes: co-evolution of tRNA and EF-Tu |
title_sort | evolutionary ‘intermediate state’ of mitochondrial translation systems found in trichinella species of parasitic nematodes: co-evolution of trna and ef-tu |
topic | RNA |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1636415/ https://www.ncbi.nlm.nih.gov/pubmed/17012285 http://dx.doi.org/10.1093/nar/gkl526 |
work_keys_str_mv | AT aritamasashi anevolutionaryintermediatestateofmitochondrialtranslationsystemsfoundintrichinellaspeciesofparasiticnematodescoevolutionoftrnaandeftu AT suematsutakuma anevolutionaryintermediatestateofmitochondrialtranslationsystemsfoundintrichinellaspeciesofparasiticnematodescoevolutionoftrnaandeftu AT osanaiarihiro anevolutionaryintermediatestateofmitochondrialtranslationsystemsfoundintrichinellaspeciesofparasiticnematodescoevolutionoftrnaandeftu AT inabatakashi anevolutionaryintermediatestateofmitochondrialtranslationsystemsfoundintrichinellaspeciesofparasiticnematodescoevolutionoftrnaandeftu AT kamiyaharuo anevolutionaryintermediatestateofmitochondrialtranslationsystemsfoundintrichinellaspeciesofparasiticnematodescoevolutionoftrnaandeftu AT kitakiyoshi anevolutionaryintermediatestateofmitochondrialtranslationsystemsfoundintrichinellaspeciesofparasiticnematodescoevolutionoftrnaandeftu AT sisidomasahiko anevolutionaryintermediatestateofmitochondrialtranslationsystemsfoundintrichinellaspeciesofparasiticnematodescoevolutionoftrnaandeftu AT watanabeyohichi anevolutionaryintermediatestateofmitochondrialtranslationsystemsfoundintrichinellaspeciesofparasiticnematodescoevolutionoftrnaandeftu AT ohtsukitakashi anevolutionaryintermediatestateofmitochondrialtranslationsystemsfoundintrichinellaspeciesofparasiticnematodescoevolutionoftrnaandeftu AT aritamasashi evolutionaryintermediatestateofmitochondrialtranslationsystemsfoundintrichinellaspeciesofparasiticnematodescoevolutionoftrnaandeftu AT suematsutakuma evolutionaryintermediatestateofmitochondrialtranslationsystemsfoundintrichinellaspeciesofparasiticnematodescoevolutionoftrnaandeftu AT osanaiarihiro evolutionaryintermediatestateofmitochondrialtranslationsystemsfoundintrichinellaspeciesofparasiticnematodescoevolutionoftrnaandeftu AT inabatakashi evolutionaryintermediatestateofmitochondrialtranslationsystemsfoundintrichinellaspeciesofparasiticnematodescoevolutionoftrnaandeftu AT kamiyaharuo evolutionaryintermediatestateofmitochondrialtranslationsystemsfoundintrichinellaspeciesofparasiticnematodescoevolutionoftrnaandeftu AT kitakiyoshi evolutionaryintermediatestateofmitochondrialtranslationsystemsfoundintrichinellaspeciesofparasiticnematodescoevolutionoftrnaandeftu AT sisidomasahiko evolutionaryintermediatestateofmitochondrialtranslationsystemsfoundintrichinellaspeciesofparasiticnematodescoevolutionoftrnaandeftu AT watanabeyohichi evolutionaryintermediatestateofmitochondrialtranslationsystemsfoundintrichinellaspeciesofparasiticnematodescoevolutionoftrnaandeftu AT ohtsukitakashi evolutionaryintermediatestateofmitochondrialtranslationsystemsfoundintrichinellaspeciesofparasiticnematodescoevolutionoftrnaandeftu |