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Unique transposon landscapes are pervasive across Drosophila melanogaster genomes
To understand how transposon landscapes (TLs) vary across animal genomes, we describe a new method called the Transposon Insertion and Depletion AnaLyzer (TIDAL) and a database of >300 TLs in Drosophila melanogaster (TIDAL-Fly). Our analysis reveals pervasive TL diversity across cell lines and fl...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678822/ https://www.ncbi.nlm.nih.gov/pubmed/26578579 http://dx.doi.org/10.1093/nar/gkv1193 |
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author | Rahman, Reazur Chirn, Gung-wei Kanodia, Abhay Sytnikova, Yuliya A. Brembs, Björn Bergman, Casey M. Lau, Nelson C. |
author_facet | Rahman, Reazur Chirn, Gung-wei Kanodia, Abhay Sytnikova, Yuliya A. Brembs, Björn Bergman, Casey M. Lau, Nelson C. |
author_sort | Rahman, Reazur |
collection | PubMed |
description | To understand how transposon landscapes (TLs) vary across animal genomes, we describe a new method called the Transposon Insertion and Depletion AnaLyzer (TIDAL) and a database of >300 TLs in Drosophila melanogaster (TIDAL-Fly). Our analysis reveals pervasive TL diversity across cell lines and fly strains, even for identically named sub-strains from different laboratories such as the ISO1 strain used for the reference genome sequence. On average, >500 novel insertions exist in every lab strain, inbred strains of the Drosophila Genetic Reference Panel (DGRP), and fly isolates in the Drosophila Genome Nexus (DGN). A minority (<25%) of transposon families comprise the majority (>70%) of TL diversity across fly strains. A sharp contrast between insertion and depletion patterns indicates that many transposons are unique to the ISO1 reference genome sequence. Although TL diversity from fly strains reaches asymptotic limits with increasing sequencing depth, rampant TL diversity causes unsaturated detection of TLs in pools of flies. Finally, we show novel transposon insertions negatively correlate with Piwi-interacting RNA (piRNA) levels for most transposon families, except for the highly-abundant roo retrotransposon. Our study provides a useful resource for Drosophila geneticists to understand how transposons create extensive genomic diversity in fly cell lines and strains. |
format | Online Article Text |
id | pubmed-4678822 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-46788222015-12-16 Unique transposon landscapes are pervasive across Drosophila melanogaster genomes Rahman, Reazur Chirn, Gung-wei Kanodia, Abhay Sytnikova, Yuliya A. Brembs, Björn Bergman, Casey M. Lau, Nelson C. Nucleic Acids Res Data Resources and Analyses To understand how transposon landscapes (TLs) vary across animal genomes, we describe a new method called the Transposon Insertion and Depletion AnaLyzer (TIDAL) and a database of >300 TLs in Drosophila melanogaster (TIDAL-Fly). Our analysis reveals pervasive TL diversity across cell lines and fly strains, even for identically named sub-strains from different laboratories such as the ISO1 strain used for the reference genome sequence. On average, >500 novel insertions exist in every lab strain, inbred strains of the Drosophila Genetic Reference Panel (DGRP), and fly isolates in the Drosophila Genome Nexus (DGN). A minority (<25%) of transposon families comprise the majority (>70%) of TL diversity across fly strains. A sharp contrast between insertion and depletion patterns indicates that many transposons are unique to the ISO1 reference genome sequence. Although TL diversity from fly strains reaches asymptotic limits with increasing sequencing depth, rampant TL diversity causes unsaturated detection of TLs in pools of flies. Finally, we show novel transposon insertions negatively correlate with Piwi-interacting RNA (piRNA) levels for most transposon families, except for the highly-abundant roo retrotransposon. Our study provides a useful resource for Drosophila geneticists to understand how transposons create extensive genomic diversity in fly cell lines and strains. Oxford University Press 2015-12-15 2015-11-17 /pmc/articles/PMC4678822/ /pubmed/26578579 http://dx.doi.org/10.1093/nar/gkv1193 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Data Resources and Analyses Rahman, Reazur Chirn, Gung-wei Kanodia, Abhay Sytnikova, Yuliya A. Brembs, Björn Bergman, Casey M. Lau, Nelson C. Unique transposon landscapes are pervasive across Drosophila melanogaster genomes |
title | Unique transposon landscapes are pervasive across Drosophila melanogaster genomes |
title_full | Unique transposon landscapes are pervasive across Drosophila melanogaster genomes |
title_fullStr | Unique transposon landscapes are pervasive across Drosophila melanogaster genomes |
title_full_unstemmed | Unique transposon landscapes are pervasive across Drosophila melanogaster genomes |
title_short | Unique transposon landscapes are pervasive across Drosophila melanogaster genomes |
title_sort | unique transposon landscapes are pervasive across drosophila melanogaster genomes |
topic | Data Resources and Analyses |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678822/ https://www.ncbi.nlm.nih.gov/pubmed/26578579 http://dx.doi.org/10.1093/nar/gkv1193 |
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