Comparative analysis of tandem repeats from hundreds of species reveals unique insights into centromere evolution

Detalhes bibliográficos
Autor(a) principal: Melters, Daniel P.
Data de Publicação: 2013
Outros Autores: Bradnam, Keith R., Young, Hugh A., Telis, Natalie, May, Michael R., Ruby, J. Graham, Sebra, Robert, Peluso, Paul, Eid, John, Rank, David, Garcia, José Fernando [UNESP], DeRisi, Joseph L., Smith, Timothy, Tobias, Christian, Ross-Ibarra, Jeffrey, Korf, Ian, Chan, Simon W. L.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1186/gb-2013-14-1-r10
http://hdl.handle.net/11449/112398
Resumo: Background: Centromeres are essential for chromosome segregation, yet their DNA sequences evolve rapidly. In most animals and plants that have been studied, centromeres contain megabase-scale arrays of tandem repeats. Despite their importance, very little is known about the degree to which centromere tandem repeats share common properties between different species across different phyla. We used bioinformatic methods to identify high-copy tandem repeats from 282 species using publicly available genomic sequence and our own data.Results: Our methods are compatible with all current sequencing technologies. Long Pacific Biosciences sequence reads allowed us to find tandem repeat monomers up to 1,419 bp. We assumed that the most abundant tandem repeat is the centromere DNA, which was true for most species whose centromeres have been previously characterized, suggesting this is a general property of genomes. High-copy centromere tandem repeats were found in almost all animal and plant genomes, but repeat monomers were highly variable in sequence composition and length. Furthermore, phylogenetic analysis of sequence homology showed little evidence of sequence conservation beyond approximately 50 million years of divergence. We find that despite an overall lack of sequence conservation, centromere tandem repeats from diverse species showed similar modes of evolution.Conclusions: While centromere position in most eukaryotes is epigenetically determined, our results indicate that tandem repeats are highly prevalent at centromeres of both animal and plant genomes. This suggests a functional role for such repeats, perhaps in promoting concerted evolution of centromere DNA across chromosomes.
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spelling Comparative analysis of tandem repeats from hundreds of species reveals unique insights into centromere evolutionBackground: Centromeres are essential for chromosome segregation, yet their DNA sequences evolve rapidly. In most animals and plants that have been studied, centromeres contain megabase-scale arrays of tandem repeats. Despite their importance, very little is known about the degree to which centromere tandem repeats share common properties between different species across different phyla. We used bioinformatic methods to identify high-copy tandem repeats from 282 species using publicly available genomic sequence and our own data.Results: Our methods are compatible with all current sequencing technologies. Long Pacific Biosciences sequence reads allowed us to find tandem repeat monomers up to 1,419 bp. We assumed that the most abundant tandem repeat is the centromere DNA, which was true for most species whose centromeres have been previously characterized, suggesting this is a general property of genomes. High-copy centromere tandem repeats were found in almost all animal and plant genomes, but repeat monomers were highly variable in sequence composition and length. Furthermore, phylogenetic analysis of sequence homology showed little evidence of sequence conservation beyond approximately 50 million years of divergence. We find that despite an overall lack of sequence conservation, centromere tandem repeats from diverse species showed similar modes of evolution.Conclusions: While centromere position in most eukaryotes is epigenetically determined, our results indicate that tandem repeats are highly prevalent at centromeres of both animal and plant genomes. This suggests a functional role for such repeats, perhaps in promoting concerted evolution of centromere DNA across chromosomes.Joint USDA/DOE Office of Science Feedstock genomics grantNational Science FoundationNIH-NIGMSUniv Calif Davis, Dept Mol & Cell Biol, Davis, CA 95616 USAUniv Calif Davis, Genome Ctr, Davis, CA 95616 USAUniv Calif Davis, Dept Plant Biol, Davis, CA 95616 USAUSDA ARS, Western Reg Res Ctr, Albany, CA 94710 USAUniv Calif Davis, Dept Ecol & Evolut, Davis, CA 95616 USAUniv Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94158 USAPacific Biosci, Menlo Pk, CA 94025 USAUniv Estadual Paulista, Dept Anim Prod & Hlth, IAEA Collaborating Ctr Anim Genom & Bioinformat, BR-16050680 Aracatuba, SP, BrazilHoward Hughes Med Inst, Chevy Chase, MD 20815 USAUSDA ARS, US Meat Anim Res Ctr, Clay Ctr, NE 68933 USAUniv Calif Davis, Dept Plant Sci, Ctr Populat Biol, Davis, CA 95616 USAUniv Estadual Paulista, Dept Anim Prod & Hlth, IAEA Collaborating Ctr Anim Genom & Bioinformat, BR-16050680 Aracatuba, SP, BrazilJoint USDA/DOE Office of Science Feedstock genomics grantDE-AI02-09ER64829National Science FoundationIOS-0922703National Science FoundationIOS-1026094NIH-NIGMST32-GM008799Biomed Central Ltd.Univ Calif DavisUSDA ARSUniv Calif San FranciscoPacific BiosciUniversidade Estadual Paulista (Unesp)Howard Hughes Med InstMelters, Daniel P.Bradnam, Keith R.Young, Hugh A.Telis, NatalieMay, Michael R.Ruby, J. GrahamSebra, RobertPeluso, PaulEid, JohnRank, DavidGarcia, José Fernando [UNESP]DeRisi, Joseph L.Smith, TimothyTobias, ChristianRoss-Ibarra, JeffreyKorf, IanChan, Simon W. L.2014-12-03T13:10:41Z2014-12-03T13:10:41Z2013-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article20application/pdfhttp://dx.doi.org/10.1186/gb-2013-14-1-r10Genome Biology. London: Biomed Central Ltd, v. 14, n. 1, 20 p., 2013.1465-6906http://hdl.handle.net/11449/11239810.1186/gb-2013-14-1-r10WOS:000320155200010WOS000320155200010.pdf9991374083045897Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengGenome Biologyinfo:eu-repo/semantics/openAccess2023-11-04T06:09:16Zoai:repositorio.unesp.br:11449/112398Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-11-04T06:09:16Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Comparative analysis of tandem repeats from hundreds of species reveals unique insights into centromere evolution
title Comparative analysis of tandem repeats from hundreds of species reveals unique insights into centromere evolution
spellingShingle Comparative analysis of tandem repeats from hundreds of species reveals unique insights into centromere evolution
Melters, Daniel P.
title_short Comparative analysis of tandem repeats from hundreds of species reveals unique insights into centromere evolution
title_full Comparative analysis of tandem repeats from hundreds of species reveals unique insights into centromere evolution
title_fullStr Comparative analysis of tandem repeats from hundreds of species reveals unique insights into centromere evolution
title_full_unstemmed Comparative analysis of tandem repeats from hundreds of species reveals unique insights into centromere evolution
title_sort Comparative analysis of tandem repeats from hundreds of species reveals unique insights into centromere evolution
author Melters, Daniel P.
author_facet Melters, Daniel P.
Bradnam, Keith R.
Young, Hugh A.
Telis, Natalie
May, Michael R.
Ruby, J. Graham
Sebra, Robert
Peluso, Paul
Eid, John
Rank, David
Garcia, José Fernando [UNESP]
DeRisi, Joseph L.
Smith, Timothy
Tobias, Christian
Ross-Ibarra, Jeffrey
Korf, Ian
Chan, Simon W. L.
author_role author
author2 Bradnam, Keith R.
Young, Hugh A.
Telis, Natalie
May, Michael R.
Ruby, J. Graham
Sebra, Robert
Peluso, Paul
Eid, John
Rank, David
Garcia, José Fernando [UNESP]
DeRisi, Joseph L.
Smith, Timothy
Tobias, Christian
Ross-Ibarra, Jeffrey
Korf, Ian
Chan, Simon W. L.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Univ Calif Davis
USDA ARS
Univ Calif San Francisco
Pacific Biosci
Universidade Estadual Paulista (Unesp)
Howard Hughes Med Inst
dc.contributor.author.fl_str_mv Melters, Daniel P.
Bradnam, Keith R.
Young, Hugh A.
Telis, Natalie
May, Michael R.
Ruby, J. Graham
Sebra, Robert
Peluso, Paul
Eid, John
Rank, David
Garcia, José Fernando [UNESP]
DeRisi, Joseph L.
Smith, Timothy
Tobias, Christian
Ross-Ibarra, Jeffrey
Korf, Ian
Chan, Simon W. L.
description Background: Centromeres are essential for chromosome segregation, yet their DNA sequences evolve rapidly. In most animals and plants that have been studied, centromeres contain megabase-scale arrays of tandem repeats. Despite their importance, very little is known about the degree to which centromere tandem repeats share common properties between different species across different phyla. We used bioinformatic methods to identify high-copy tandem repeats from 282 species using publicly available genomic sequence and our own data.Results: Our methods are compatible with all current sequencing technologies. Long Pacific Biosciences sequence reads allowed us to find tandem repeat monomers up to 1,419 bp. We assumed that the most abundant tandem repeat is the centromere DNA, which was true for most species whose centromeres have been previously characterized, suggesting this is a general property of genomes. High-copy centromere tandem repeats were found in almost all animal and plant genomes, but repeat monomers were highly variable in sequence composition and length. Furthermore, phylogenetic analysis of sequence homology showed little evidence of sequence conservation beyond approximately 50 million years of divergence. We find that despite an overall lack of sequence conservation, centromere tandem repeats from diverse species showed similar modes of evolution.Conclusions: While centromere position in most eukaryotes is epigenetically determined, our results indicate that tandem repeats are highly prevalent at centromeres of both animal and plant genomes. This suggests a functional role for such repeats, perhaps in promoting concerted evolution of centromere DNA across chromosomes.
publishDate 2013
dc.date.none.fl_str_mv 2013-01-01
2014-12-03T13:10:41Z
2014-12-03T13:10:41Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1186/gb-2013-14-1-r10
Genome Biology. London: Biomed Central Ltd, v. 14, n. 1, 20 p., 2013.
1465-6906
http://hdl.handle.net/11449/112398
10.1186/gb-2013-14-1-r10
WOS:000320155200010
WOS000320155200010.pdf
9991374083045897
url http://dx.doi.org/10.1186/gb-2013-14-1-r10
http://hdl.handle.net/11449/112398
identifier_str_mv Genome Biology. London: Biomed Central Ltd, v. 14, n. 1, 20 p., 2013.
1465-6906
10.1186/gb-2013-14-1-r10
WOS:000320155200010
WOS000320155200010.pdf
9991374083045897
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Genome Biology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 20
application/pdf
dc.publisher.none.fl_str_mv Biomed Central Ltd.
publisher.none.fl_str_mv Biomed Central Ltd.
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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