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Cross-Kingdom Commonality of a Novel Insertion Signature of RTE-Related Short Retroposons

In multicellular organisms, such as vertebrates and flowering plants, horizontal transfer (HT) of genetic information is thought to be a rare event. However, recent findings unveiled unexpectedly frequent HT of RTE-clade LINEs. To elucidate the molecular footprints of the genomic integration machine...

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Autores principales: Nishiyama, Eri, Ohshima, Kazuhiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6007223/
https://www.ncbi.nlm.nih.gov/pubmed/29850801
http://dx.doi.org/10.1093/gbe/evy098
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author Nishiyama, Eri
Ohshima, Kazuhiko
author_facet Nishiyama, Eri
Ohshima, Kazuhiko
author_sort Nishiyama, Eri
collection PubMed
description In multicellular organisms, such as vertebrates and flowering plants, horizontal transfer (HT) of genetic information is thought to be a rare event. However, recent findings unveiled unexpectedly frequent HT of RTE-clade LINEs. To elucidate the molecular footprints of the genomic integration machinery of RTE-related retroposons, the sequence patterns surrounding the insertion sites of plant Au-like SINE families were analyzed in the genomes of a wide variety of flowering plants. A novel and remarkable finding regarding target site duplications (TSDs) for SINEs was they start with thymine approximately one helical pitch (ten nucleotides) downstream of a thymine stretch. This TSD pattern was found in RTE-clade LINEs, which share the 3′-end sequence of these SINEs, in the genome of leguminous plants. These results demonstrably show that Au-like SINEs were mobilized by the enzymatic machinery of RTE-clade LINEs. Further, we discovered the same TSD pattern in animal SINEs from lizard and mammals, in which the RTE-clade LINEs sharing the 3′-end sequence with these animal SINEs showed a distinct TSD pattern. Moreover, a significant correlation was observed between the first nucleotide of TSDs and microsatellite-like sequences found at the 3′-ends of SINEs and LINEs. We propose that RTE-encoded protein could preferentially bind to a DNA region that contains a thymine stretch to cleave a phosphodiester bond downstream of the stretch. Further, determination of cleavage sites and/or efficiency of primer sites for reverse transcription may depend on microsatellite-like repeats in the RNA template. Such a unique mechanism may have enabled retroposons to successfully expand in frontier genomes after HT.
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spelling pubmed-60072232018-06-25 Cross-Kingdom Commonality of a Novel Insertion Signature of RTE-Related Short Retroposons Nishiyama, Eri Ohshima, Kazuhiko Genome Biol Evol Research Article In multicellular organisms, such as vertebrates and flowering plants, horizontal transfer (HT) of genetic information is thought to be a rare event. However, recent findings unveiled unexpectedly frequent HT of RTE-clade LINEs. To elucidate the molecular footprints of the genomic integration machinery of RTE-related retroposons, the sequence patterns surrounding the insertion sites of plant Au-like SINE families were analyzed in the genomes of a wide variety of flowering plants. A novel and remarkable finding regarding target site duplications (TSDs) for SINEs was they start with thymine approximately one helical pitch (ten nucleotides) downstream of a thymine stretch. This TSD pattern was found in RTE-clade LINEs, which share the 3′-end sequence of these SINEs, in the genome of leguminous plants. These results demonstrably show that Au-like SINEs were mobilized by the enzymatic machinery of RTE-clade LINEs. Further, we discovered the same TSD pattern in animal SINEs from lizard and mammals, in which the RTE-clade LINEs sharing the 3′-end sequence with these animal SINEs showed a distinct TSD pattern. Moreover, a significant correlation was observed between the first nucleotide of TSDs and microsatellite-like sequences found at the 3′-ends of SINEs and LINEs. We propose that RTE-encoded protein could preferentially bind to a DNA region that contains a thymine stretch to cleave a phosphodiester bond downstream of the stretch. Further, determination of cleavage sites and/or efficiency of primer sites for reverse transcription may depend on microsatellite-like repeats in the RNA template. Such a unique mechanism may have enabled retroposons to successfully expand in frontier genomes after HT. Oxford University Press 2018-05-29 /pmc/articles/PMC6007223/ /pubmed/29850801 http://dx.doi.org/10.1093/gbe/evy098 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Nishiyama, Eri
Ohshima, Kazuhiko
Cross-Kingdom Commonality of a Novel Insertion Signature of RTE-Related Short Retroposons
title Cross-Kingdom Commonality of a Novel Insertion Signature of RTE-Related Short Retroposons
title_full Cross-Kingdom Commonality of a Novel Insertion Signature of RTE-Related Short Retroposons
title_fullStr Cross-Kingdom Commonality of a Novel Insertion Signature of RTE-Related Short Retroposons
title_full_unstemmed Cross-Kingdom Commonality of a Novel Insertion Signature of RTE-Related Short Retroposons
title_short Cross-Kingdom Commonality of a Novel Insertion Signature of RTE-Related Short Retroposons
title_sort cross-kingdom commonality of a novel insertion signature of rte-related short retroposons
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6007223/
https://www.ncbi.nlm.nih.gov/pubmed/29850801
http://dx.doi.org/10.1093/gbe/evy098
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