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Three-dimensional structure model and predicted ATP interaction rewiring of a deviant RNA ligase 2

BACKGROUND: RNA ligases 2 are scarce and scattered across the tree of life. Two members of this family are well studied: the mitochondrial RNA editing ligase from the parasitic trypanosomes (Kinetoplastea), a promising drug target, and bacteriophage T4 RNA ligase 2, a workhorse in molecular biology....

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Autores principales: Moreira, Sandrine, Noutahi, Emmanuel, Lamoureux, Guillaume, Burger, Gertraud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4599027/
https://www.ncbi.nlm.nih.gov/pubmed/26449279
http://dx.doi.org/10.1186/s12900-015-0046-0
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author Moreira, Sandrine
Noutahi, Emmanuel
Lamoureux, Guillaume
Burger, Gertraud
author_facet Moreira, Sandrine
Noutahi, Emmanuel
Lamoureux, Guillaume
Burger, Gertraud
author_sort Moreira, Sandrine
collection PubMed
description BACKGROUND: RNA ligases 2 are scarce and scattered across the tree of life. Two members of this family are well studied: the mitochondrial RNA editing ligase from the parasitic trypanosomes (Kinetoplastea), a promising drug target, and bacteriophage T4 RNA ligase 2, a workhorse in molecular biology. Here we report the identification of a divergent RNA ligase 2 (DpRNL) from Diplonema papillatum (Diplonemea), a member of the kinetoplastids’ sister group. METHODS: We identified DpRNL with methods based on sensitive hidden Markov Model. Then, using homology modeling and molecular dynamics simulations, we established a three dimensional structure model of DpRNL complexed with ATP and Mg2+. RESULTS: The 3D model of Diplonema was compared with available crystal structures from Trypanosoma brucei, bacteriophage T4, and two archaeans. Interaction of DpRNL with ATP is predicted to involve double π-stacking, which has not been reported before in RNA ligases. This particular contact would shift the orientation of ATP and have considerable consequences on the interaction network of amino acids in the catalytic pocket. We postulate that certain canonical amino acids assume different functional roles in DpRNL compared to structurally homologous residues in other RNA ligases 2, a reassignment indicative of constructive neutral evolution. Finally, both structure comparison and phylogenetic analysis show that DpRNL is not specifically related to RNA ligases from trypanosomes, suggesting a unique adaptation of the latter for RNA editing, after the split of diplonemids and kinetoplastids. CONCLUSION: Homology modeling and molecular dynamics simulations strongly suggest that DpRNL is an RNA ligase 2. The predicted innovative reshaping of DpRNL’s catalytic pocket is worthwhile to be tested experimentally. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12900-015-0046-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-45990272015-10-09 Three-dimensional structure model and predicted ATP interaction rewiring of a deviant RNA ligase 2 Moreira, Sandrine Noutahi, Emmanuel Lamoureux, Guillaume Burger, Gertraud BMC Struct Biol Research Article BACKGROUND: RNA ligases 2 are scarce and scattered across the tree of life. Two members of this family are well studied: the mitochondrial RNA editing ligase from the parasitic trypanosomes (Kinetoplastea), a promising drug target, and bacteriophage T4 RNA ligase 2, a workhorse in molecular biology. Here we report the identification of a divergent RNA ligase 2 (DpRNL) from Diplonema papillatum (Diplonemea), a member of the kinetoplastids’ sister group. METHODS: We identified DpRNL with methods based on sensitive hidden Markov Model. Then, using homology modeling and molecular dynamics simulations, we established a three dimensional structure model of DpRNL complexed with ATP and Mg2+. RESULTS: The 3D model of Diplonema was compared with available crystal structures from Trypanosoma brucei, bacteriophage T4, and two archaeans. Interaction of DpRNL with ATP is predicted to involve double π-stacking, which has not been reported before in RNA ligases. This particular contact would shift the orientation of ATP and have considerable consequences on the interaction network of amino acids in the catalytic pocket. We postulate that certain canonical amino acids assume different functional roles in DpRNL compared to structurally homologous residues in other RNA ligases 2, a reassignment indicative of constructive neutral evolution. Finally, both structure comparison and phylogenetic analysis show that DpRNL is not specifically related to RNA ligases from trypanosomes, suggesting a unique adaptation of the latter for RNA editing, after the split of diplonemids and kinetoplastids. CONCLUSION: Homology modeling and molecular dynamics simulations strongly suggest that DpRNL is an RNA ligase 2. The predicted innovative reshaping of DpRNL’s catalytic pocket is worthwhile to be tested experimentally. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12900-015-0046-0) contains supplementary material, which is available to authorized users. BioMed Central 2015-10-09 /pmc/articles/PMC4599027/ /pubmed/26449279 http://dx.doi.org/10.1186/s12900-015-0046-0 Text en © Moreira et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Moreira, Sandrine
Noutahi, Emmanuel
Lamoureux, Guillaume
Burger, Gertraud
Three-dimensional structure model and predicted ATP interaction rewiring of a deviant RNA ligase 2
title Three-dimensional structure model and predicted ATP interaction rewiring of a deviant RNA ligase 2
title_full Three-dimensional structure model and predicted ATP interaction rewiring of a deviant RNA ligase 2
title_fullStr Three-dimensional structure model and predicted ATP interaction rewiring of a deviant RNA ligase 2
title_full_unstemmed Three-dimensional structure model and predicted ATP interaction rewiring of a deviant RNA ligase 2
title_short Three-dimensional structure model and predicted ATP interaction rewiring of a deviant RNA ligase 2
title_sort three-dimensional structure model and predicted atp interaction rewiring of a deviant rna ligase 2
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4599027/
https://www.ncbi.nlm.nih.gov/pubmed/26449279
http://dx.doi.org/10.1186/s12900-015-0046-0
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