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Forensic pregnancy diagnostics with placental mRNA markers
Current methods for pregnancy diagnostics are based on immunodetection of pregnancy-specific proteins and in a forensic context suffer from sensitivity and specificity issues. Here, we applied reverse transcriptase polymerase chain reaction (RT-PCR) technology to 11 genes previously reported with pl...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Springer-Verlag
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2795858/ https://www.ncbi.nlm.nih.gov/pubmed/19148664 http://dx.doi.org/10.1007/s00414-008-0315-6 |
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author | Gauvin, Jeanot Zubakov, Dmitry van Rhee-Binkhorst, Joke Kloosterman, Ate Steegers, Eric Kayser, Manfred |
author_facet | Gauvin, Jeanot Zubakov, Dmitry van Rhee-Binkhorst, Joke Kloosterman, Ate Steegers, Eric Kayser, Manfred |
author_sort | Gauvin, Jeanot |
collection | PubMed |
description | Current methods for pregnancy diagnostics are based on immunodetection of pregnancy-specific proteins and in a forensic context suffer from sensitivity and specificity issues. Here, we applied reverse transcriptase polymerase chain reaction (RT-PCR) technology to 11 genes previously reported with placental mRNA circulating in maternal blood. We found two genes, hPL and βhCG, with pregnancy-specific expression in whole blood samples. RT-PCR detection of hPL was positive in all samples tested throughout the pregnancy, whereas βhCG was detectable until half of the second trimester but not at later gestation ages. For hPL, in vitro stability of the transcript was demonstrated until 2 months of age, and the hPL-specific RT-PCR assay applied was highly sensitive with reliable detection from down to 0.25 cm(2) dried bloodstain. We therefore suggest hPL-specific RT-PCR as a new molecular tool for forensic pregnancy diagnostics from dried blood stains. Moreover, our results indicate that the time-wise reverse expression of hPL and βhCG during pregnancy may allow an RT-PCR-based estimation of the gestational age from blood stains, adding to the value of forensic pregnancy diagnosis for crime scene investigations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00414-008-0315-6) contains supplementary material, which is available to authorized users. |
format | Text |
id | pubmed-2795858 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-27958582009-12-23 Forensic pregnancy diagnostics with placental mRNA markers Gauvin, Jeanot Zubakov, Dmitry van Rhee-Binkhorst, Joke Kloosterman, Ate Steegers, Eric Kayser, Manfred Int J Legal Med Original Article Current methods for pregnancy diagnostics are based on immunodetection of pregnancy-specific proteins and in a forensic context suffer from sensitivity and specificity issues. Here, we applied reverse transcriptase polymerase chain reaction (RT-PCR) technology to 11 genes previously reported with placental mRNA circulating in maternal blood. We found two genes, hPL and βhCG, with pregnancy-specific expression in whole blood samples. RT-PCR detection of hPL was positive in all samples tested throughout the pregnancy, whereas βhCG was detectable until half of the second trimester but not at later gestation ages. For hPL, in vitro stability of the transcript was demonstrated until 2 months of age, and the hPL-specific RT-PCR assay applied was highly sensitive with reliable detection from down to 0.25 cm(2) dried bloodstain. We therefore suggest hPL-specific RT-PCR as a new molecular tool for forensic pregnancy diagnostics from dried blood stains. Moreover, our results indicate that the time-wise reverse expression of hPL and βhCG during pregnancy may allow an RT-PCR-based estimation of the gestational age from blood stains, adding to the value of forensic pregnancy diagnosis for crime scene investigations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00414-008-0315-6) contains supplementary material, which is available to authorized users. Springer-Verlag 2009-01-16 2010 /pmc/articles/PMC2795858/ /pubmed/19148664 http://dx.doi.org/10.1007/s00414-008-0315-6 Text en © The Author(s) 2009 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Original Article Gauvin, Jeanot Zubakov, Dmitry van Rhee-Binkhorst, Joke Kloosterman, Ate Steegers, Eric Kayser, Manfred Forensic pregnancy diagnostics with placental mRNA markers |
title | Forensic pregnancy diagnostics with placental mRNA markers |
title_full | Forensic pregnancy diagnostics with placental mRNA markers |
title_fullStr | Forensic pregnancy diagnostics with placental mRNA markers |
title_full_unstemmed | Forensic pregnancy diagnostics with placental mRNA markers |
title_short | Forensic pregnancy diagnostics with placental mRNA markers |
title_sort | forensic pregnancy diagnostics with placental mrna markers |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2795858/ https://www.ncbi.nlm.nih.gov/pubmed/19148664 http://dx.doi.org/10.1007/s00414-008-0315-6 |
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