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X-ray structure of the fourth type of archaeal tRNA splicing endonuclease: insights into the evolution of a novel three-unit composition and a unique loop involved in broad substrate specificity
Cleavage of introns from precursor transfer RNAs (tRNAs) by tRNA splicing endonuclease (EndA) is essential for tRNA maturation in Archaea and Eukarya. In the past, archaeal EndAs were classified into three types (α′(2), α(4 )and α(2)β(2)) according to subunit composition. Recently, we have identifie...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3488258/ https://www.ncbi.nlm.nih.gov/pubmed/22941657 http://dx.doi.org/10.1093/nar/gks826 |
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author | Hirata, Akira Fujishima, Kosuke Yamagami, Ryota Kawamura, Takuya Banfield, Jillian F. Kanai, Akio Hori, Hiroyuki |
author_facet | Hirata, Akira Fujishima, Kosuke Yamagami, Ryota Kawamura, Takuya Banfield, Jillian F. Kanai, Akio Hori, Hiroyuki |
author_sort | Hirata, Akira |
collection | PubMed |
description | Cleavage of introns from precursor transfer RNAs (tRNAs) by tRNA splicing endonuclease (EndA) is essential for tRNA maturation in Archaea and Eukarya. In the past, archaeal EndAs were classified into three types (α′(2), α(4 )and α(2)β(2)) according to subunit composition. Recently, we have identified a fourth type of archaeal EndA from an uncultivated archaeon Candidatus Micrarchaeum acidiphilum, referred to as ARMAN-2, which is deeply branched within Euryarchaea. The ARMAN-2 EndA forms an ε(2) homodimer and has broad substrate specificity like the α(2)β(2 )type EndAs found in Crenarchaea and Nanoarchaea. However, the precise architecture of ARMAN-2 EndA was unknown. Here, we report the crystal structure of the ε(2) homodimer of ARMAN-2 EndA. The structure reveals that the ε protomer is separated into three novel units (α(N), α and β(C)) fused by two distinct linkers, although the overall structure of ARMAN-2 EndA is similar to those of the other three types of archaeal EndAs. Structural comparison and mutational analyses reveal that an ARMAN-2 type-specific loop (ASL) is involved in the broad substrate specificity and that K161 in the ASL functions as the RNA recognition site. These findings suggest that the broad substrate specificities of ε(2) and α(2)β(2) EndAs were separately acquired through different evolutionary processes. |
format | Online Article Text |
id | pubmed-3488258 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-34882582012-11-06 X-ray structure of the fourth type of archaeal tRNA splicing endonuclease: insights into the evolution of a novel three-unit composition and a unique loop involved in broad substrate specificity Hirata, Akira Fujishima, Kosuke Yamagami, Ryota Kawamura, Takuya Banfield, Jillian F. Kanai, Akio Hori, Hiroyuki Nucleic Acids Res Structural Biology Cleavage of introns from precursor transfer RNAs (tRNAs) by tRNA splicing endonuclease (EndA) is essential for tRNA maturation in Archaea and Eukarya. In the past, archaeal EndAs were classified into three types (α′(2), α(4 )and α(2)β(2)) according to subunit composition. Recently, we have identified a fourth type of archaeal EndA from an uncultivated archaeon Candidatus Micrarchaeum acidiphilum, referred to as ARMAN-2, which is deeply branched within Euryarchaea. The ARMAN-2 EndA forms an ε(2) homodimer and has broad substrate specificity like the α(2)β(2 )type EndAs found in Crenarchaea and Nanoarchaea. However, the precise architecture of ARMAN-2 EndA was unknown. Here, we report the crystal structure of the ε(2) homodimer of ARMAN-2 EndA. The structure reveals that the ε protomer is separated into three novel units (α(N), α and β(C)) fused by two distinct linkers, although the overall structure of ARMAN-2 EndA is similar to those of the other three types of archaeal EndAs. Structural comparison and mutational analyses reveal that an ARMAN-2 type-specific loop (ASL) is involved in the broad substrate specificity and that K161 in the ASL functions as the RNA recognition site. These findings suggest that the broad substrate specificities of ε(2) and α(2)β(2) EndAs were separately acquired through different evolutionary processes. Oxford University Press 2012-11 2012-08-30 /pmc/articles/PMC3488258/ /pubmed/22941657 http://dx.doi.org/10.1093/nar/gks826 Text en © The Author(s) 2012. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Structural Biology Hirata, Akira Fujishima, Kosuke Yamagami, Ryota Kawamura, Takuya Banfield, Jillian F. Kanai, Akio Hori, Hiroyuki X-ray structure of the fourth type of archaeal tRNA splicing endonuclease: insights into the evolution of a novel three-unit composition and a unique loop involved in broad substrate specificity |
title | X-ray structure of the fourth type of archaeal tRNA splicing endonuclease: insights into the evolution of a novel three-unit composition and a unique loop involved in broad substrate specificity |
title_full | X-ray structure of the fourth type of archaeal tRNA splicing endonuclease: insights into the evolution of a novel three-unit composition and a unique loop involved in broad substrate specificity |
title_fullStr | X-ray structure of the fourth type of archaeal tRNA splicing endonuclease: insights into the evolution of a novel three-unit composition and a unique loop involved in broad substrate specificity |
title_full_unstemmed | X-ray structure of the fourth type of archaeal tRNA splicing endonuclease: insights into the evolution of a novel three-unit composition and a unique loop involved in broad substrate specificity |
title_short | X-ray structure of the fourth type of archaeal tRNA splicing endonuclease: insights into the evolution of a novel three-unit composition and a unique loop involved in broad substrate specificity |
title_sort | x-ray structure of the fourth type of archaeal trna splicing endonuclease: insights into the evolution of a novel three-unit composition and a unique loop involved in broad substrate specificity |
topic | Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3488258/ https://www.ncbi.nlm.nih.gov/pubmed/22941657 http://dx.doi.org/10.1093/nar/gks826 |
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