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The Isolation of Nucleic Acids from Fixed, Paraffin-Embedded Tissues–Which Methods Are Useful When?

Museums and pathology collections around the world represent an archive of genetic material to study populations and diseases. For preservation purposes, a large portion of these collections has been fixed in formalin-containing solutions, a treatment that results in cross-linking of biomolecules. C...

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Autores principales: Gilbert, M. Thomas P., Haselkorn, Tamara, Bunce, Michael, Sanchez, Juan J., Lucas, Sebastian B., Jewell, Laurence D., Marck, Eric Van, Worobey, Michael
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1888728/
https://www.ncbi.nlm.nih.gov/pubmed/17579711
http://dx.doi.org/10.1371/journal.pone.0000537
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author Gilbert, M. Thomas P.
Haselkorn, Tamara
Bunce, Michael
Sanchez, Juan J.
Lucas, Sebastian B.
Jewell, Laurence D.
Marck, Eric Van
Worobey, Michael
author_facet Gilbert, M. Thomas P.
Haselkorn, Tamara
Bunce, Michael
Sanchez, Juan J.
Lucas, Sebastian B.
Jewell, Laurence D.
Marck, Eric Van
Worobey, Michael
author_sort Gilbert, M. Thomas P.
collection PubMed
description Museums and pathology collections around the world represent an archive of genetic material to study populations and diseases. For preservation purposes, a large portion of these collections has been fixed in formalin-containing solutions, a treatment that results in cross-linking of biomolecules. Cross-linking not only complicates isolation of nucleic acid but also introduces polymerase “blocks” during PCR. A wide variety of methods exists for the recovery of DNA and RNA from archival tissues, and although a number of previous studies have qualitatively compared the relative merits of the different techniques, very few have undertaken wide scale quantitative comparisons. To help address this issue, we have undertaken a study that investigates the quality of nucleic acids recovered from a test panel of fixed specimens that have been manipulated following a number of the published protocols. These include methods of pre-treating the samples prior to extraction, extraction and nucleic acid purification methods themselves, and a post-extraction enzymatic repair technique. We find that although many of the published methods have distinct positive effects on some characteristics of the nucleic acids, the benefits often come at a cost. In addition, a number of the previously published techniques appear to have no effect at all. Our findings recommend that the extraction methodology adopted should be chosen carefully. Here we provide a quick reference table that can be used to determine appropriate protocols for particular aims.
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spelling pubmed-18887282007-06-20 The Isolation of Nucleic Acids from Fixed, Paraffin-Embedded Tissues–Which Methods Are Useful When? Gilbert, M. Thomas P. Haselkorn, Tamara Bunce, Michael Sanchez, Juan J. Lucas, Sebastian B. Jewell, Laurence D. Marck, Eric Van Worobey, Michael PLoS One Research Article Museums and pathology collections around the world represent an archive of genetic material to study populations and diseases. For preservation purposes, a large portion of these collections has been fixed in formalin-containing solutions, a treatment that results in cross-linking of biomolecules. Cross-linking not only complicates isolation of nucleic acid but also introduces polymerase “blocks” during PCR. A wide variety of methods exists for the recovery of DNA and RNA from archival tissues, and although a number of previous studies have qualitatively compared the relative merits of the different techniques, very few have undertaken wide scale quantitative comparisons. To help address this issue, we have undertaken a study that investigates the quality of nucleic acids recovered from a test panel of fixed specimens that have been manipulated following a number of the published protocols. These include methods of pre-treating the samples prior to extraction, extraction and nucleic acid purification methods themselves, and a post-extraction enzymatic repair technique. We find that although many of the published methods have distinct positive effects on some characteristics of the nucleic acids, the benefits often come at a cost. In addition, a number of the previously published techniques appear to have no effect at all. Our findings recommend that the extraction methodology adopted should be chosen carefully. Here we provide a quick reference table that can be used to determine appropriate protocols for particular aims. Public Library of Science 2007-06-20 /pmc/articles/PMC1888728/ /pubmed/17579711 http://dx.doi.org/10.1371/journal.pone.0000537 Text en Gilbert et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Gilbert, M. Thomas P.
Haselkorn, Tamara
Bunce, Michael
Sanchez, Juan J.
Lucas, Sebastian B.
Jewell, Laurence D.
Marck, Eric Van
Worobey, Michael
The Isolation of Nucleic Acids from Fixed, Paraffin-Embedded Tissues–Which Methods Are Useful When?
title The Isolation of Nucleic Acids from Fixed, Paraffin-Embedded Tissues–Which Methods Are Useful When?
title_full The Isolation of Nucleic Acids from Fixed, Paraffin-Embedded Tissues–Which Methods Are Useful When?
title_fullStr The Isolation of Nucleic Acids from Fixed, Paraffin-Embedded Tissues–Which Methods Are Useful When?
title_full_unstemmed The Isolation of Nucleic Acids from Fixed, Paraffin-Embedded Tissues–Which Methods Are Useful When?
title_short The Isolation of Nucleic Acids from Fixed, Paraffin-Embedded Tissues–Which Methods Are Useful When?
title_sort isolation of nucleic acids from fixed, paraffin-embedded tissues–which methods are useful when?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1888728/
https://www.ncbi.nlm.nih.gov/pubmed/17579711
http://dx.doi.org/10.1371/journal.pone.0000537
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