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Utility of arsenic-treated bird skins for DNA extraction

BACKGROUND: Natural history museums receive a rapidly growing number of requests for tissue samples from preserved specimens for DNA-based studies. Traditionally, dried vertebrate specimens were treated with arsenic because of its toxicity and insect-repellent effect. Arsenic has negative effects on...

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Autores principales: Töpfer, Till, Gamauf, Anita, Haring, Elisabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3138465/
https://www.ncbi.nlm.nih.gov/pubmed/21676254
http://dx.doi.org/10.1186/1756-0500-4-197
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author Töpfer, Till
Gamauf, Anita
Haring, Elisabeth
author_facet Töpfer, Till
Gamauf, Anita
Haring, Elisabeth
author_sort Töpfer, Till
collection PubMed
description BACKGROUND: Natural history museums receive a rapidly growing number of requests for tissue samples from preserved specimens for DNA-based studies. Traditionally, dried vertebrate specimens were treated with arsenic because of its toxicity and insect-repellent effect. Arsenic has negative effects on in vivo DNA repair enzymes and consequently may inhibit PCR performance. In bird collections, foot pad samples are often requested since the feet were not regularly treated with arsenic and because they are assumed to provide substantial amounts of DNA. However, the actual influence of arsenic on DNA analyses has never been tested. FINDINGS: PCR success of both foot pad and body skin samples was significantly lower in arsenic-treated samples. In general, foot pads performed better than body skin samples. Moreover, PCR success depends on collection date in which younger samples yielded better results. While the addition of arsenic solution to the PCR mixture had a clear negative effect on PCR performance after the threshold of 5.4 μg/μl, such high doses of arsenic are highly unlikely to occur in dried zoological specimens. CONCLUSIONS: While lower PCR success in older samples might be due to age effects and/or DNA damage through arsenic treatment, our results show no inhibiting effect on DNA polymerase. We assume that DNA degradation proceeds more rapidly in thin tissue layers with low cell numbers that are susceptible to external abiotic influences. In contrast, in thicker parts of a specimen, such as foot pads, the outermost horny skin may act as an additional barrier. Since foot pads often performed better than body skin samples, the intention to preserve morphologically important structures of a specimen still conflicts with the aim to obtain optimal PCR success. Thus, body skin samples from recently collected specimens should be considered as alternative sources of DNA.
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spelling pubmed-31384652011-07-19 Utility of arsenic-treated bird skins for DNA extraction Töpfer, Till Gamauf, Anita Haring, Elisabeth BMC Res Notes Short Report BACKGROUND: Natural history museums receive a rapidly growing number of requests for tissue samples from preserved specimens for DNA-based studies. Traditionally, dried vertebrate specimens were treated with arsenic because of its toxicity and insect-repellent effect. Arsenic has negative effects on in vivo DNA repair enzymes and consequently may inhibit PCR performance. In bird collections, foot pad samples are often requested since the feet were not regularly treated with arsenic and because they are assumed to provide substantial amounts of DNA. However, the actual influence of arsenic on DNA analyses has never been tested. FINDINGS: PCR success of both foot pad and body skin samples was significantly lower in arsenic-treated samples. In general, foot pads performed better than body skin samples. Moreover, PCR success depends on collection date in which younger samples yielded better results. While the addition of arsenic solution to the PCR mixture had a clear negative effect on PCR performance after the threshold of 5.4 μg/μl, such high doses of arsenic are highly unlikely to occur in dried zoological specimens. CONCLUSIONS: While lower PCR success in older samples might be due to age effects and/or DNA damage through arsenic treatment, our results show no inhibiting effect on DNA polymerase. We assume that DNA degradation proceeds more rapidly in thin tissue layers with low cell numbers that are susceptible to external abiotic influences. In contrast, in thicker parts of a specimen, such as foot pads, the outermost horny skin may act as an additional barrier. Since foot pads often performed better than body skin samples, the intention to preserve morphologically important structures of a specimen still conflicts with the aim to obtain optimal PCR success. Thus, body skin samples from recently collected specimens should be considered as alternative sources of DNA. BioMed Central 2011-06-15 /pmc/articles/PMC3138465/ /pubmed/21676254 http://dx.doi.org/10.1186/1756-0500-4-197 Text en Copyright ©2011 Töpfer et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Report
Töpfer, Till
Gamauf, Anita
Haring, Elisabeth
Utility of arsenic-treated bird skins for DNA extraction
title Utility of arsenic-treated bird skins for DNA extraction
title_full Utility of arsenic-treated bird skins for DNA extraction
title_fullStr Utility of arsenic-treated bird skins for DNA extraction
title_full_unstemmed Utility of arsenic-treated bird skins for DNA extraction
title_short Utility of arsenic-treated bird skins for DNA extraction
title_sort utility of arsenic-treated bird skins for dna extraction
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3138465/
https://www.ncbi.nlm.nih.gov/pubmed/21676254
http://dx.doi.org/10.1186/1756-0500-4-197
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