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Repeated horizontal transfers of four DNA transposons in invertebrates and bats
BACKGROUND: Horizontal transfer (HT) of transposable elements (TEs) into a new genome is considered as an important force to drive genome variation and biological innovation. However, most of the HT of DNA transposons previously described occurred between closely related species or insects. RESULTS:...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298943/ https://www.ncbi.nlm.nih.gov/pubmed/25606061 http://dx.doi.org/10.1186/s13100-014-0033-1 |
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author | Tang, Zhou Zhang, Hua-Hao Huang, Ke Zhang, Xiao-Gu Han, Min-Jin Zhang, Ze |
author_facet | Tang, Zhou Zhang, Hua-Hao Huang, Ke Zhang, Xiao-Gu Han, Min-Jin Zhang, Ze |
author_sort | Tang, Zhou |
collection | PubMed |
description | BACKGROUND: Horizontal transfer (HT) of transposable elements (TEs) into a new genome is considered as an important force to drive genome variation and biological innovation. However, most of the HT of DNA transposons previously described occurred between closely related species or insects. RESULTS: In this study, we carried out a detailed analysis of four DNA transposons, which were found in the first sequenced twisted-wing parasite, Mengenilla moldrzyki. Through the homology-based strategy, these transposons were also identified in other insects, freshwater planarian, hydrozoans, and bats. The phylogenetic distribution of these transposons was discontinuous, and they showed extremely high sequence identities (>87%) over their entire length in spite of their hosts diverging more than 300 million years ago (Mya). Additionally, phylogenies and comparisons of transposons versus orthologous gene identities demonstrated that these transposons have transferred into their hosts by independent HTs. CONCLUSIONS: Here, we provided the first documented example of HT of CACTA transposons, which have been so far extensively studied in plants. Our results demonstrated that bats had continuously acquired new DNA elements via HT. This implies that predation on a large quantity of insects might increase bat exposure to HT. In addition, parasite-host interaction might facilitate exchanging of their genetic materials. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13100-014-0033-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4298943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42989432015-01-21 Repeated horizontal transfers of four DNA transposons in invertebrates and bats Tang, Zhou Zhang, Hua-Hao Huang, Ke Zhang, Xiao-Gu Han, Min-Jin Zhang, Ze Mob DNA Research BACKGROUND: Horizontal transfer (HT) of transposable elements (TEs) into a new genome is considered as an important force to drive genome variation and biological innovation. However, most of the HT of DNA transposons previously described occurred between closely related species or insects. RESULTS: In this study, we carried out a detailed analysis of four DNA transposons, which were found in the first sequenced twisted-wing parasite, Mengenilla moldrzyki. Through the homology-based strategy, these transposons were also identified in other insects, freshwater planarian, hydrozoans, and bats. The phylogenetic distribution of these transposons was discontinuous, and they showed extremely high sequence identities (>87%) over their entire length in spite of their hosts diverging more than 300 million years ago (Mya). Additionally, phylogenies and comparisons of transposons versus orthologous gene identities demonstrated that these transposons have transferred into their hosts by independent HTs. CONCLUSIONS: Here, we provided the first documented example of HT of CACTA transposons, which have been so far extensively studied in plants. Our results demonstrated that bats had continuously acquired new DNA elements via HT. This implies that predation on a large quantity of insects might increase bat exposure to HT. In addition, parasite-host interaction might facilitate exchanging of their genetic materials. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13100-014-0033-1) contains supplementary material, which is available to authorized users. BioMed Central 2015-01-17 /pmc/articles/PMC4298943/ /pubmed/25606061 http://dx.doi.org/10.1186/s13100-014-0033-1 Text en © Tang et al.; licensee BioMed Central. 2015 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 work is properly credited. 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 Tang, Zhou Zhang, Hua-Hao Huang, Ke Zhang, Xiao-Gu Han, Min-Jin Zhang, Ze Repeated horizontal transfers of four DNA transposons in invertebrates and bats |
title | Repeated horizontal transfers of four DNA transposons in invertebrates and bats |
title_full | Repeated horizontal transfers of four DNA transposons in invertebrates and bats |
title_fullStr | Repeated horizontal transfers of four DNA transposons in invertebrates and bats |
title_full_unstemmed | Repeated horizontal transfers of four DNA transposons in invertebrates and bats |
title_short | Repeated horizontal transfers of four DNA transposons in invertebrates and bats |
title_sort | repeated horizontal transfers of four dna transposons in invertebrates and bats |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298943/ https://www.ncbi.nlm.nih.gov/pubmed/25606061 http://dx.doi.org/10.1186/s13100-014-0033-1 |
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