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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...

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Autores principales: Hirata, Akira, Fujishima, Kosuke, Yamagami, Ryota, Kawamura, Takuya, Banfield, Jillian F., Kanai, Akio, Hori, Hiroyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
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.
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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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