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...
- 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)
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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 |
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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 |
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https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0028448&type=printable |
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http://purl.org/coar/access_right/c_abf2 |
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Abierto (Texto Completo) |
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Abierto (Texto Completo) http://purl.org/coar/access_right/c_abf2 |
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PLOS Public Library of Science |
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PLoS One |
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Universidad del Rosario |
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