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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Nucleic acids research 2015-12, Vol.43 (22), p.10655-10672
Hauptverfasser: Rahman, Reazur, Chirn, Gung-wei, Kanodia, Abhay, Sytnikova, Yuliya A, Brembs, Björn, Bergman, Casey M, Lau, Nelson C
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 10672
container_issue 22
container_start_page 10655
container_title Nucleic acids research
container_volume 43
creator Rahman, Reazur
Chirn, Gung-wei
Kanodia, Abhay
Sytnikova, Yuliya A
Brembs, Björn
Bergman, Casey M
Lau, Nelson C
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 (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.
doi_str_mv 10.1093/nar/gkv1193
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4678822</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1749999916</sourcerecordid><originalsourceid>FETCH-LOGICAL-c344t-55dfe12792838dcb56fa78269a25c808924ffb41e9483771bfaaf18e64eb317d3</originalsourceid><addsrcrecordid>eNpVkd1LwzAUxYMobk6ffJc-ClKXrzbJiyDzEwYiuOeQtrdbtW1q0hX8783cHHofch_y4yTnHITOCb4mWLFpa9x0-TEQotgBGhOW0pirlB6iMWY4iQnmcoROvH_HmHCS8GM0omkiZCLUGL0u2upzDVHvTOs7620b1aYtfG468JFxEHXgBuOrASKTO-t9dBdO262q2kQNBNguje_BRUtobQP-FB2VpvZwttsTtHi4f5s9xfOXx-fZ7TzOGed9nCRFCYQKRSWTRZ4laWmEpKkyNMklloryssw4AcUlE4JkpTElkZByyBgRBZugm61ut84aKHJog4dad65qjPvS1lT6_01brfTSDpqnQkpKg8DlTsDZEIHvdVP5HOpgCezaayK42gxJA3q1RX8ScFDunyFYb0rQoQS9KyHQF39_tmd_U2ff9ceGpA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1749999916</pqid></control><display><type>article</type><title>Unique transposon landscapes are pervasive across Drosophila melanogaster genomes</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>Oxford Journals Open Access Collection</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><creator>Rahman, Reazur ; Chirn, Gung-wei ; Kanodia, Abhay ; Sytnikova, Yuliya A ; Brembs, Björn ; Bergman, Casey M ; Lau, Nelson C</creator><creatorcontrib>Rahman, Reazur ; Chirn, Gung-wei ; Kanodia, Abhay ; Sytnikova, Yuliya A ; Brembs, Björn ; Bergman, Casey M ; Lau, Nelson C</creatorcontrib><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 &gt;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, &gt;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 (&lt;25%) of transposon families comprise the majority (&gt;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.</description><identifier>ISSN: 0305-1048</identifier><identifier>EISSN: 1362-4962</identifier><identifier>DOI: 10.1093/nar/gkv1193</identifier><identifier>PMID: 26578579</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Animals ; Cell Line ; Data Resources and Analyses ; Databases, Nucleic Acid ; DNA Transposable Elements ; Drosophila melanogaster - genetics ; Genetic Variation ; Genome, Insect ; Genomics - methods ; Retroelements ; RNA, Small Interfering - metabolism</subject><ispartof>Nucleic acids research, 2015-12, Vol.43 (22), p.10655-10672</ispartof><rights>The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research.</rights><rights>The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c344t-55dfe12792838dcb56fa78269a25c808924ffb41e9483771bfaaf18e64eb317d3</citedby><cites>FETCH-LOGICAL-c344t-55dfe12792838dcb56fa78269a25c808924ffb41e9483771bfaaf18e64eb317d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678822/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678822/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,861,882,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26578579$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rahman, Reazur</creatorcontrib><creatorcontrib>Chirn, Gung-wei</creatorcontrib><creatorcontrib>Kanodia, Abhay</creatorcontrib><creatorcontrib>Sytnikova, Yuliya A</creatorcontrib><creatorcontrib>Brembs, Björn</creatorcontrib><creatorcontrib>Bergman, Casey M</creatorcontrib><creatorcontrib>Lau, Nelson C</creatorcontrib><title>Unique transposon landscapes are pervasive across Drosophila melanogaster genomes</title><title>Nucleic acids research</title><addtitle>Nucleic Acids Res</addtitle><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 &gt;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, &gt;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 (&lt;25%) of transposon families comprise the majority (&gt;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.</description><subject>Animals</subject><subject>Cell Line</subject><subject>Data Resources and Analyses</subject><subject>Databases, Nucleic Acid</subject><subject>DNA Transposable Elements</subject><subject>Drosophila melanogaster - genetics</subject><subject>Genetic Variation</subject><subject>Genome, Insect</subject><subject>Genomics - methods</subject><subject>Retroelements</subject><subject>RNA, Small Interfering - metabolism</subject><issn>0305-1048</issn><issn>1362-4962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkd1LwzAUxYMobk6ffJc-ClKXrzbJiyDzEwYiuOeQtrdbtW1q0hX8783cHHofch_y4yTnHITOCb4mWLFpa9x0-TEQotgBGhOW0pirlB6iMWY4iQnmcoROvH_HmHCS8GM0omkiZCLUGL0u2upzDVHvTOs7620b1aYtfG468JFxEHXgBuOrASKTO-t9dBdO262q2kQNBNguje_BRUtobQP-FB2VpvZwttsTtHi4f5s9xfOXx-fZ7TzOGed9nCRFCYQKRSWTRZ4laWmEpKkyNMklloryssw4AcUlE4JkpTElkZByyBgRBZugm61ut84aKHJog4dad65qjPvS1lT6_01brfTSDpqnQkpKg8DlTsDZEIHvdVP5HOpgCezaayK42gxJA3q1RX8ScFDunyFYb0rQoQS9KyHQF39_tmd_U2ff9ceGpA</recordid><startdate>20151215</startdate><enddate>20151215</enddate><creator>Rahman, Reazur</creator><creator>Chirn, Gung-wei</creator><creator>Kanodia, Abhay</creator><creator>Sytnikova, Yuliya A</creator><creator>Brembs, Björn</creator><creator>Bergman, Casey M</creator><creator>Lau, Nelson C</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20151215</creationdate><title>Unique transposon landscapes are pervasive across Drosophila melanogaster genomes</title><author>Rahman, Reazur ; Chirn, Gung-wei ; Kanodia, Abhay ; Sytnikova, Yuliya A ; Brembs, Björn ; Bergman, Casey M ; Lau, Nelson C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c344t-55dfe12792838dcb56fa78269a25c808924ffb41e9483771bfaaf18e64eb317d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Cell Line</topic><topic>Data Resources and Analyses</topic><topic>Databases, Nucleic Acid</topic><topic>DNA Transposable Elements</topic><topic>Drosophila melanogaster - genetics</topic><topic>Genetic Variation</topic><topic>Genome, Insect</topic><topic>Genomics - methods</topic><topic>Retroelements</topic><topic>RNA, Small Interfering - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rahman, Reazur</creatorcontrib><creatorcontrib>Chirn, Gung-wei</creatorcontrib><creatorcontrib>Kanodia, Abhay</creatorcontrib><creatorcontrib>Sytnikova, Yuliya A</creatorcontrib><creatorcontrib>Brembs, Björn</creatorcontrib><creatorcontrib>Bergman, Casey M</creatorcontrib><creatorcontrib>Lau, Nelson C</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nucleic acids research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rahman, Reazur</au><au>Chirn, Gung-wei</au><au>Kanodia, Abhay</au><au>Sytnikova, Yuliya A</au><au>Brembs, Björn</au><au>Bergman, Casey M</au><au>Lau, Nelson C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Unique transposon landscapes are pervasive across Drosophila melanogaster genomes</atitle><jtitle>Nucleic acids research</jtitle><addtitle>Nucleic Acids Res</addtitle><date>2015-12-15</date><risdate>2015</risdate><volume>43</volume><issue>22</issue><spage>10655</spage><epage>10672</epage><pages>10655-10672</pages><issn>0305-1048</issn><eissn>1362-4962</eissn><abstract>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 &gt;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, &gt;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 (&lt;25%) of transposon families comprise the majority (&gt;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.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>26578579</pmid><doi>10.1093/nar/gkv1193</doi><tpages>18</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0305-1048
ispartof Nucleic acids research, 2015-12, Vol.43 (22), p.10655-10672
issn 0305-1048
1362-4962
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4678822
source MEDLINE; DOAJ Directory of Open Access Journals; Oxford Journals Open Access Collection; PubMed Central; Free Full-Text Journals in Chemistry
subjects Animals
Cell Line
Data Resources and Analyses
Databases, Nucleic Acid
DNA Transposable Elements
Drosophila melanogaster - genetics
Genetic Variation
Genome, Insect
Genomics - methods
Retroelements
RNA, Small Interfering - metabolism
title Unique transposon landscapes are pervasive across Drosophila melanogaster genomes
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-20T02%3A51%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Unique%20transposon%20landscapes%20are%20pervasive%20across%20Drosophila%20melanogaster%20genomes&rft.jtitle=Nucleic%20acids%20research&rft.au=Rahman,%20Reazur&rft.date=2015-12-15&rft.volume=43&rft.issue=22&rft.spage=10655&rft.epage=10672&rft.pages=10655-10672&rft.issn=0305-1048&rft.eissn=1362-4962&rft_id=info:doi/10.1093/nar/gkv1193&rft_dat=%3Cproquest_pubme%3E1749999916%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1749999916&rft_id=info:pmid/26578579&rfr_iscdi=true