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Identification of RAG-like transposons in protostomes suggests their ancient bilaterian origin

BACKGROUND: V(D) J recombination is essential for adaptive immunity in jawed vertebrates and is initiated by the RAG1-RAG2 endonuclease. The RAG1 and RAG2 genes are thought to have evolved from a RAGL (RAG-like) transposon containing convergently-oriented RAG1-like (RAG1L) and RAG2-like (RAG2L) gene...

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Autores principales: Martin, Eliza C., Vicari, Célia, Tsakou-Ngouafo, Louis, Pontarotti, Pierre, Petrescu, Andrei J., Schatz, David G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7204232/
https://www.ncbi.nlm.nih.gov/pubmed/32399063
http://dx.doi.org/10.1186/s13100-020-00214-y
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author Martin, Eliza C.
Vicari, Célia
Tsakou-Ngouafo, Louis
Pontarotti, Pierre
Petrescu, Andrei J.
Schatz, David G.
author_facet Martin, Eliza C.
Vicari, Célia
Tsakou-Ngouafo, Louis
Pontarotti, Pierre
Petrescu, Andrei J.
Schatz, David G.
author_sort Martin, Eliza C.
collection PubMed
description BACKGROUND: V(D) J recombination is essential for adaptive immunity in jawed vertebrates and is initiated by the RAG1-RAG2 endonuclease. The RAG1 and RAG2 genes are thought to have evolved from a RAGL (RAG-like) transposon containing convergently-oriented RAG1-like (RAG1L) and RAG2-like (RAG2L) genes. Elements resembling this presumptive evolutionary precursor have thus far only been detected convincingly in deuterostomes, leading to the model that the RAGL transposon first appeared in an early deuterostome. RESULTS: We have identified numerous RAGL transposons in the genomes of protostomes, including oysters and mussels (phylum Mollusca) and a ribbon worm (phylum Nemertea), and in the genomes of several cnidarians. Phylogenetic analyses are consistent with vertical evolution of RAGL transposons within the Bilateria clade and with its presence in the bilaterian ancestor. Many of the RAGL transposons identified in protostomes are intact elements containing convergently oriented RAG1L and RAG2L genes flanked by terminal inverted repeats (TIRs) and target site duplications with striking similarities with the corresponding elements in deuterostomes. In addition, protostome genomes contain numerous intact RAG1L-RAG2L adjacent gene pairs that lack detectable flanking TIRs. Domains and critical active site and structural amino acids needed for endonuclease and transposase activity are present and conserved in many of the predicted RAG1L and RAG2L proteins encoded in protostome genomes. CONCLUSIONS: Active RAGL transposons were present in multiple protostome lineages and many were likely transmitted vertically during protostome evolution. It appears that RAGL transposons were broadly active during bilaterian evolution, undergoing multiple duplication and loss/fossilization events, with the RAGL genes that persist in present day protostomes perhaps constituting both active RAGL transposons and domesticated RAGL genes. Our findings raise the possibility that the RAGL transposon arose earlier in evolution than previously thought, either in an early bilaterian or prior to the divergence of bilaterians and non-bilaterians, and alter our understanding of the evolutionary history of this important group of transposons.
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spelling pubmed-72042322020-05-12 Identification of RAG-like transposons in protostomes suggests their ancient bilaterian origin Martin, Eliza C. Vicari, Célia Tsakou-Ngouafo, Louis Pontarotti, Pierre Petrescu, Andrei J. Schatz, David G. Mob DNA Research BACKGROUND: V(D) J recombination is essential for adaptive immunity in jawed vertebrates and is initiated by the RAG1-RAG2 endonuclease. The RAG1 and RAG2 genes are thought to have evolved from a RAGL (RAG-like) transposon containing convergently-oriented RAG1-like (RAG1L) and RAG2-like (RAG2L) genes. Elements resembling this presumptive evolutionary precursor have thus far only been detected convincingly in deuterostomes, leading to the model that the RAGL transposon first appeared in an early deuterostome. RESULTS: We have identified numerous RAGL transposons in the genomes of protostomes, including oysters and mussels (phylum Mollusca) and a ribbon worm (phylum Nemertea), and in the genomes of several cnidarians. Phylogenetic analyses are consistent with vertical evolution of RAGL transposons within the Bilateria clade and with its presence in the bilaterian ancestor. Many of the RAGL transposons identified in protostomes are intact elements containing convergently oriented RAG1L and RAG2L genes flanked by terminal inverted repeats (TIRs) and target site duplications with striking similarities with the corresponding elements in deuterostomes. In addition, protostome genomes contain numerous intact RAG1L-RAG2L adjacent gene pairs that lack detectable flanking TIRs. Domains and critical active site and structural amino acids needed for endonuclease and transposase activity are present and conserved in many of the predicted RAG1L and RAG2L proteins encoded in protostome genomes. CONCLUSIONS: Active RAGL transposons were present in multiple protostome lineages and many were likely transmitted vertically during protostome evolution. It appears that RAGL transposons were broadly active during bilaterian evolution, undergoing multiple duplication and loss/fossilization events, with the RAGL genes that persist in present day protostomes perhaps constituting both active RAGL transposons and domesticated RAGL genes. Our findings raise the possibility that the RAGL transposon arose earlier in evolution than previously thought, either in an early bilaterian or prior to the divergence of bilaterians and non-bilaterians, and alter our understanding of the evolutionary history of this important group of transposons. BioMed Central 2020-05-06 /pmc/articles/PMC7204232/ /pubmed/32399063 http://dx.doi.org/10.1186/s13100-020-00214-y Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research
Martin, Eliza C.
Vicari, Célia
Tsakou-Ngouafo, Louis
Pontarotti, Pierre
Petrescu, Andrei J.
Schatz, David G.
Identification of RAG-like transposons in protostomes suggests their ancient bilaterian origin
title Identification of RAG-like transposons in protostomes suggests their ancient bilaterian origin
title_full Identification of RAG-like transposons in protostomes suggests their ancient bilaterian origin
title_fullStr Identification of RAG-like transposons in protostomes suggests their ancient bilaterian origin
title_full_unstemmed Identification of RAG-like transposons in protostomes suggests their ancient bilaterian origin
title_short Identification of RAG-like transposons in protostomes suggests their ancient bilaterian origin
title_sort identification of rag-like transposons in protostomes suggests their ancient bilaterian origin
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7204232/
https://www.ncbi.nlm.nih.gov/pubmed/32399063
http://dx.doi.org/10.1186/s13100-020-00214-y
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