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LTR-mediated retroposition as a mechanism of RNA-based duplication in metazoans
In a broad range of taxa, genes can duplicate through an RNA intermediate in a process mediated by retrotransposons (retroposition). In mammals, L1 retrotransposons drive retroposition, but the elements responsible for retroposition in other animals have yet to be identified. Here, we examined young...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5131818/ https://www.ncbi.nlm.nih.gov/pubmed/27934698 http://dx.doi.org/10.1101/gr.204925.116 |
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author | Tan, Shengjun Cardoso-Moreira, Margarida Shi, Wenwen Zhang, Dan Huang, Jiawei Mao, Yanan Jia, Hangxing Zhang, Yaqiong Chen, Chunyan Shao, Yi Leng, Liang Liu, Zhonghua Huang, Xun Long, Manyuan Zhang, Yong E. |
author_facet | Tan, Shengjun Cardoso-Moreira, Margarida Shi, Wenwen Zhang, Dan Huang, Jiawei Mao, Yanan Jia, Hangxing Zhang, Yaqiong Chen, Chunyan Shao, Yi Leng, Liang Liu, Zhonghua Huang, Xun Long, Manyuan Zhang, Yong E. |
author_sort | Tan, Shengjun |
collection | PubMed |
description | In a broad range of taxa, genes can duplicate through an RNA intermediate in a process mediated by retrotransposons (retroposition). In mammals, L1 retrotransposons drive retroposition, but the elements responsible for retroposition in other animals have yet to be identified. Here, we examined young retrocopies from various animals that still retain the sequence features indicative of the underlying retroposition mechanism. In Drosophila melanogaster, we identified and de novo assembled 15 polymorphic retrocopies and found that all retroposed loci are chimeras of internal retrocopies flanked by discontinuous LTR retrotransposons. At the fusion points between the mRNAs and the LTR retrotransposons, we identified shared short similar sequences that suggest the involvement of microsimilarity-dependent template switches. By expanding our approach to mosquito, zebrafish, chicken, and mammals, we identified in all these species recently originated retrocopies with a similar chimeric structure and shared microsimilarities at the fusion points. We also identified several retrocopies that combine the sequences of two or more parental genes, demonstrating LTR-retroposition as a novel mechanism of exon shuffling. Finally, we found that LTR-mediated retrocopies are immediately cotranscribed with their flanking LTR retrotransposons. Transcriptional profiling coupled with sequence analyses revealed that the sense-strand transcription of the retrocopies often lead to the origination of in-frame proteins relative to the parental genes. Overall, our data show that LTR-mediated retroposition is highly conserved across a wide range of animal taxa; combined with previous work from plants and yeast, it represents an ancient and ongoing mechanism continuously shaping gene content evolution in eukaryotes. |
format | Online Article Text |
id | pubmed-5131818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-51318182016-12-19 LTR-mediated retroposition as a mechanism of RNA-based duplication in metazoans Tan, Shengjun Cardoso-Moreira, Margarida Shi, Wenwen Zhang, Dan Huang, Jiawei Mao, Yanan Jia, Hangxing Zhang, Yaqiong Chen, Chunyan Shao, Yi Leng, Liang Liu, Zhonghua Huang, Xun Long, Manyuan Zhang, Yong E. Genome Res Research In a broad range of taxa, genes can duplicate through an RNA intermediate in a process mediated by retrotransposons (retroposition). In mammals, L1 retrotransposons drive retroposition, but the elements responsible for retroposition in other animals have yet to be identified. Here, we examined young retrocopies from various animals that still retain the sequence features indicative of the underlying retroposition mechanism. In Drosophila melanogaster, we identified and de novo assembled 15 polymorphic retrocopies and found that all retroposed loci are chimeras of internal retrocopies flanked by discontinuous LTR retrotransposons. At the fusion points between the mRNAs and the LTR retrotransposons, we identified shared short similar sequences that suggest the involvement of microsimilarity-dependent template switches. By expanding our approach to mosquito, zebrafish, chicken, and mammals, we identified in all these species recently originated retrocopies with a similar chimeric structure and shared microsimilarities at the fusion points. We also identified several retrocopies that combine the sequences of two or more parental genes, demonstrating LTR-retroposition as a novel mechanism of exon shuffling. Finally, we found that LTR-mediated retrocopies are immediately cotranscribed with their flanking LTR retrotransposons. Transcriptional profiling coupled with sequence analyses revealed that the sense-strand transcription of the retrocopies often lead to the origination of in-frame proteins relative to the parental genes. Overall, our data show that LTR-mediated retroposition is highly conserved across a wide range of animal taxa; combined with previous work from plants and yeast, it represents an ancient and ongoing mechanism continuously shaping gene content evolution in eukaryotes. Cold Spring Harbor Laboratory Press 2016-12 /pmc/articles/PMC5131818/ /pubmed/27934698 http://dx.doi.org/10.1101/gr.204925.116 Text en © 2016 Tan et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article, published in Genome Research, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Research Tan, Shengjun Cardoso-Moreira, Margarida Shi, Wenwen Zhang, Dan Huang, Jiawei Mao, Yanan Jia, Hangxing Zhang, Yaqiong Chen, Chunyan Shao, Yi Leng, Liang Liu, Zhonghua Huang, Xun Long, Manyuan Zhang, Yong E. LTR-mediated retroposition as a mechanism of RNA-based duplication in metazoans |
title | LTR-mediated retroposition as a mechanism of RNA-based duplication in metazoans |
title_full | LTR-mediated retroposition as a mechanism of RNA-based duplication in metazoans |
title_fullStr | LTR-mediated retroposition as a mechanism of RNA-based duplication in metazoans |
title_full_unstemmed | LTR-mediated retroposition as a mechanism of RNA-based duplication in metazoans |
title_short | LTR-mediated retroposition as a mechanism of RNA-based duplication in metazoans |
title_sort | ltr-mediated retroposition as a mechanism of rna-based duplication in metazoans |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5131818/ https://www.ncbi.nlm.nih.gov/pubmed/27934698 http://dx.doi.org/10.1101/gr.204925.116 |
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