DNA damage in plant herbarium tissue

Dried plant herbarium specimens are potentially a valuable source of DNA. Efforts to obtain genetic information from this source are often hindered by an inability to obtain amplifiable DNA as herbarium DNA is typically highly degraded. DNA post-mortem damage may not only reduce the number of amplif...

Full description

Autores:
Tipo de recurso:
Fecha de publicación:
2011
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/27537
Acceso en línea:
https://doi.org/10.1371/journal.pone.0028448
https://repository.urosario.edu.co/handle/10336/27537
Palabra clave:
DNA damage
Plastids Mitochondria
Polymerase chain reaction
Nucleotides
DNA
DNA extraction
Specimen preparation and treatment
Rights
License
Abierto (Texto Completo)
id EDOCUR2_5d7f43b0f2a2902632d0ac33fedd0890
oai_identifier_str oai:repository.urosario.edu.co:10336/27537
network_acronym_str EDOCUR2
network_name_str Repositorio EdocUR - U. Rosario
repository_id_str
spelling 2ce3b586-d630-4455-995a-4df4e001ff56ba2815d5-4a1e-4c77-bd48-71ff569b4b283593286000eb454ea-53ba-4c15-a997-cc58e8ca45235a43d0c5-30f7-4bdf-8630-54b560d76815a2a252be-3ccc-4b72-aa30-ca9980623c28d9a781e3-f89b-4265-81d3-b81bbb7caf3c2020-08-19T14:42:37Z2020-08-19T14:42:37Z2011-12-05Dried plant herbarium specimens are potentially a valuable source of DNA. Efforts to obtain genetic information from this source are often hindered by an inability to obtain amplifiable DNA as herbarium DNA is typically highly degraded. DNA post-mortem damage may not only reduce the number of amplifiable template molecules, but may also lead to the generation of erroneous sequence information. A qualitative and quantitative assessment of DNA post-mortem damage is essential to determine the accuracy of molecular data from herbarium specimens. In this study we present an assessment of DNA damage as miscoding lesions in herbarium specimens using 454-sequencing of amplicons derived from plastid, mitochondrial, and nuclear DNA. In addition, we assess DNA degradation as a result of strand breaks and other types of polymerase non-bypassable damage by quantitative real-time PCR. Comparing four pairs of fresh and herbarium specimens of the same individuals we quantitatively assess post-mortem DNA damage, directly after specimen preparation, as well as after long-term herbarium storage. After specimen preparation we estimate the proportion of gene copy numbers of plastid, mitochondrial, and nuclear DNA to be 2.4–3.8% of fresh control DNA and 1.0–1.3% after long-term herbarium storage, indicating that nearly all DNA damage occurs on specimen preparation. In addition, there is no evidence of preferential degradation of organelle versus nuclear genomes. Increased levels of C?T/G?A transitions were observed in old herbarium plastid DNA, representing 21.8% of observed miscoding lesions. We interpret this type of post-mortem DNA damage-derived modification to have arisen from the hydrolytic deamination of cytosine during long-term herbarium storage. Our results suggest that reliable sequence data can be obtained from herbarium specimens.application/pdfhttps://doi.org/10.1371/journal.pone.0028448EISSN: 1932-6203https://repository.urosario.edu.co/handle/10336/27537engPLOS Public Library of ScienceNo. 12e28448PLoS OneVol. 6PLoS One, EISSN: 1932-6203, Vol.6, No.12 (December 2011); pp. e28448https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0028448&type=printableAbierto (Texto Completo)http://purl.org/coar/access_right/c_abf2PLoS Oneinstname:Universidad del Rosarioreponame:Repositorio Institucional EdocURDNA damagePlastids MitochondriaPolymerase chain reactionNucleotidesDNADNA extractionSpecimen preparation and treatmentDNA damage in plant herbarium tissueDaño del ADN en el tejido del herbario vegetalarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Staats, MartijnCuenca, ArgeliaRichardson, James-EdwardVrielink-van Ginkel, RiaPetersen, GitteSeberg, OleBakker, Freek T.ORIGINALjournal-pone-0028448.pdfapplication/pdf209072https://repository.urosario.edu.co/bitstreams/e671fce2-eca5-42d1-8f61-3dd5b1700ea8/download1ee600f08e8a5fa0432422c3bc9ba2f7MD51TEXTjournal-pone-0028448.pdf.txtjournal-pone-0028448.pdf.txtExtracted texttext/plain51905https://repository.urosario.edu.co/bitstreams/a523f76b-82a7-48c4-9cf6-43cc3fc641e4/downloadf9094a16dcb90f97807b935416e3645fMD52THUMBNAILjournal-pone-0028448.pdf.jpgjournal-pone-0028448.pdf.jpgGenerated Thumbnailimage/jpeg4810https://repository.urosario.edu.co/bitstreams/fdc68f60-dc92-4705-bbb5-3b0603638234/download55348cf20d03217eef31e56e09bb4f5aMD5310336/27537oai:repository.urosario.edu.co:10336/275372021-10-07 23:41:28.279https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co
dc.title.spa.fl_str_mv DNA damage in plant herbarium tissue
dc.title.TranslatedTitle.spa.fl_str_mv Daño del ADN en el tejido del herbario vegetal
title DNA damage in plant herbarium tissue
spellingShingle DNA damage in plant herbarium tissue
DNA damage
Plastids Mitochondria
Polymerase chain reaction
Nucleotides
DNA
DNA extraction
Specimen preparation and treatment
title_short DNA damage in plant herbarium tissue
title_full DNA damage in plant herbarium tissue
title_fullStr DNA damage in plant herbarium tissue
title_full_unstemmed DNA damage in plant herbarium tissue
title_sort DNA damage in plant herbarium tissue
dc.subject.keyword.spa.fl_str_mv DNA damage
Plastids Mitochondria
Polymerase chain reaction
Nucleotides
DNA
DNA extraction
Specimen preparation and treatment
topic DNA damage
Plastids Mitochondria
Polymerase chain reaction
Nucleotides
DNA
DNA extraction
Specimen preparation and treatment
description Dried plant herbarium specimens are potentially a valuable source of DNA. Efforts to obtain genetic information from this source are often hindered by an inability to obtain amplifiable DNA as herbarium DNA is typically highly degraded. DNA post-mortem damage may not only reduce the number of amplifiable template molecules, but may also lead to the generation of erroneous sequence information. A qualitative and quantitative assessment of DNA post-mortem damage is essential to determine the accuracy of molecular data from herbarium specimens. In this study we present an assessment of DNA damage as miscoding lesions in herbarium specimens using 454-sequencing of amplicons derived from plastid, mitochondrial, and nuclear DNA. In addition, we assess DNA degradation as a result of strand breaks and other types of polymerase non-bypassable damage by quantitative real-time PCR. Comparing four pairs of fresh and herbarium specimens of the same individuals we quantitatively assess post-mortem DNA damage, directly after specimen preparation, as well as after long-term herbarium storage. After specimen preparation we estimate the proportion of gene copy numbers of plastid, mitochondrial, and nuclear DNA to be 2.4–3.8% of fresh control DNA and 1.0–1.3% after long-term herbarium storage, indicating that nearly all DNA damage occurs on specimen preparation. In addition, there is no evidence of preferential degradation of organelle versus nuclear genomes. Increased levels of C?T/G?A transitions were observed in old herbarium plastid DNA, representing 21.8% of observed miscoding lesions. We interpret this type of post-mortem DNA damage-derived modification to have arisen from the hydrolytic deamination of cytosine during long-term herbarium storage. Our results suggest that reliable sequence data can be obtained from herbarium specimens.
publishDate 2011
dc.date.created.spa.fl_str_mv 2011-12-05
dc.date.accessioned.none.fl_str_mv 2020-08-19T14:42:37Z
dc.date.available.none.fl_str_mv 2020-08-19T14:42:37Z
dc.type.eng.fl_str_mv article
dc.type.coarversion.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.coar.fl_str_mv http://purl.org/coar/resource_type/c_6501
dc.type.spa.spa.fl_str_mv Artículo
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1371/journal.pone.0028448
dc.identifier.issn.none.fl_str_mv EISSN: 1932-6203
dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/27537
url https://doi.org/10.1371/journal.pone.0028448
https://repository.urosario.edu.co/handle/10336/27537
identifier_str_mv EISSN: 1932-6203
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.citationIssue.none.fl_str_mv No. 12
dc.relation.citationStartPage.none.fl_str_mv e28448
dc.relation.citationTitle.none.fl_str_mv PLoS One
dc.relation.citationVolume.none.fl_str_mv Vol. 6
dc.relation.ispartof.spa.fl_str_mv PLoS One, EISSN: 1932-6203, Vol.6, No.12 (December 2011); pp. e28448
dc.relation.uri.spa.fl_str_mv https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0028448&type=printable
dc.rights.coar.fl_str_mv http://purl.org/coar/access_right/c_abf2
dc.rights.acceso.spa.fl_str_mv Abierto (Texto Completo)
rights_invalid_str_mv Abierto (Texto Completo)
http://purl.org/coar/access_right/c_abf2
dc.format.mimetype.none.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv PLOS Public Library of Science
dc.source.spa.fl_str_mv PLoS One
institution Universidad del Rosario
dc.source.instname.none.fl_str_mv instname:Universidad del Rosario
dc.source.reponame.none.fl_str_mv reponame:Repositorio Institucional EdocUR
bitstream.url.fl_str_mv https://repository.urosario.edu.co/bitstreams/e671fce2-eca5-42d1-8f61-3dd5b1700ea8/download
https://repository.urosario.edu.co/bitstreams/a523f76b-82a7-48c4-9cf6-43cc3fc641e4/download
https://repository.urosario.edu.co/bitstreams/fdc68f60-dc92-4705-bbb5-3b0603638234/download
bitstream.checksum.fl_str_mv 1ee600f08e8a5fa0432422c3bc9ba2f7
f9094a16dcb90f97807b935416e3645f
55348cf20d03217eef31e56e09bb4f5a
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
MD5
repository.name.fl_str_mv Repositorio institucional EdocUR
repository.mail.fl_str_mv edocur@urosario.edu.co
_version_ 1831928199709196288