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The Wide Distribution and Change of Target Specificity of R2 Non-LTR Retrotransposons in Animals

Transposons, or transposable elements, are the major components of genomes in most eukaryotes. Some groups of transposons have developed target specificity that limits the integration sites to a specific nonessential sequence or a genomic region to avoid gene disruption caused by insertion into an e...

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Autores principales: Kojima, Kenji K., Seto, Yosuke, Fujiwara, Haruhiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5035012/
https://www.ncbi.nlm.nih.gov/pubmed/27662593
http://dx.doi.org/10.1371/journal.pone.0163496
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author Kojima, Kenji K.
Seto, Yosuke
Fujiwara, Haruhiko
author_facet Kojima, Kenji K.
Seto, Yosuke
Fujiwara, Haruhiko
author_sort Kojima, Kenji K.
collection PubMed
description Transposons, or transposable elements, are the major components of genomes in most eukaryotes. Some groups of transposons have developed target specificity that limits the integration sites to a specific nonessential sequence or a genomic region to avoid gene disruption caused by insertion into an essential gene. R2 is one of the most intensively investigated groups of sequence-specific non-LTR retrotransposons and is inserted at a specific site inside of 28S ribosomal RNA (rRNA) genes. R2 is known to be distributed among at least six animal phyla even though its occurrence is reported to be patchy. Here, in order to obtain a more detailed picture of the distribution of R2, we surveyed R2 using both in silico screening and degenerate PCR, particularly focusing on actinopterygian fish. We found two families of the R2C lineage from vertebrates, although it has previously only been found in platyhelminthes. We also revealed the apparent movement of insertion sites of a lineage of actinopterygian R2, which was likely concurrent with the acquisition of a 28S rRNA-derived sequence in their 3′ UTR. Outside of actinopterygian fish, we revealed the maintenance of a single R2 lineage in birds; the co-existence of four lineages of R2 in the leafcutter bee Megachile rotundata; the first examples of R2 in Ctenophora, Mollusca, and Hemichordata; and two families of R2 showing no target specificity. These findings indicate that R2 is relatively stable and universal, while differences in the distribution and maintenance of R2 lineages probably reflect characteristics of some combination of both R2 lineages and host organisms.
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spelling pubmed-50350122016-10-10 The Wide Distribution and Change of Target Specificity of R2 Non-LTR Retrotransposons in Animals Kojima, Kenji K. Seto, Yosuke Fujiwara, Haruhiko PLoS One Research Article Transposons, or transposable elements, are the major components of genomes in most eukaryotes. Some groups of transposons have developed target specificity that limits the integration sites to a specific nonessential sequence or a genomic region to avoid gene disruption caused by insertion into an essential gene. R2 is one of the most intensively investigated groups of sequence-specific non-LTR retrotransposons and is inserted at a specific site inside of 28S ribosomal RNA (rRNA) genes. R2 is known to be distributed among at least six animal phyla even though its occurrence is reported to be patchy. Here, in order to obtain a more detailed picture of the distribution of R2, we surveyed R2 using both in silico screening and degenerate PCR, particularly focusing on actinopterygian fish. We found two families of the R2C lineage from vertebrates, although it has previously only been found in platyhelminthes. We also revealed the apparent movement of insertion sites of a lineage of actinopterygian R2, which was likely concurrent with the acquisition of a 28S rRNA-derived sequence in their 3′ UTR. Outside of actinopterygian fish, we revealed the maintenance of a single R2 lineage in birds; the co-existence of four lineages of R2 in the leafcutter bee Megachile rotundata; the first examples of R2 in Ctenophora, Mollusca, and Hemichordata; and two families of R2 showing no target specificity. These findings indicate that R2 is relatively stable and universal, while differences in the distribution and maintenance of R2 lineages probably reflect characteristics of some combination of both R2 lineages and host organisms. Public Library of Science 2016-09-23 /pmc/articles/PMC5035012/ /pubmed/27662593 http://dx.doi.org/10.1371/journal.pone.0163496 Text en © 2016 Kojima et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kojima, Kenji K.
Seto, Yosuke
Fujiwara, Haruhiko
The Wide Distribution and Change of Target Specificity of R2 Non-LTR Retrotransposons in Animals
title The Wide Distribution and Change of Target Specificity of R2 Non-LTR Retrotransposons in Animals
title_full The Wide Distribution and Change of Target Specificity of R2 Non-LTR Retrotransposons in Animals
title_fullStr The Wide Distribution and Change of Target Specificity of R2 Non-LTR Retrotransposons in Animals
title_full_unstemmed The Wide Distribution and Change of Target Specificity of R2 Non-LTR Retrotransposons in Animals
title_short The Wide Distribution and Change of Target Specificity of R2 Non-LTR Retrotransposons in Animals
title_sort wide distribution and change of target specificity of r2 non-ltr retrotransposons in animals
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5035012/
https://www.ncbi.nlm.nih.gov/pubmed/27662593
http://dx.doi.org/10.1371/journal.pone.0163496
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