Literature DB >> 18298493

Recovery and stability of RNA in vaginal swabs and blood, semen, and saliva stains.

Mindy Setzer1, Jane Juusola, Jack Ballantyne.   

Abstract

RNA expression patterns, including the presence and relative abundance of particular mRNA species, provide cell and tissue specific information that could be used for body fluid identification. In this report, we address perceived concerns on the stability, and hence recoverability, of RNA in forensic samples. Stains were prepared from blood, saliva, semen, and vaginal secretions and exposed to a range of environmental conditions from 1 to 547 days. The persistence and stability of RNA within each type of body fluid stain were determined by quantitation of total RNA, and reverse transcriptase-polymerase chain reaction (RT-PCR) using eight different mRNA transcripts from selected housekeeping and tissue-specific genes. The results demonstrate that RNA can be recovered from biological stains in sufficient quantity and quality for mRNA analysis. On average, several hundred nanograms of total RNA was recovered from 50-microL-sized blood and saliva stains, 1 microg from a 50-microL semen stain and nearly 70 microg from a whole vaginal swab. Messenger RNA is detectable in some samples stored at room temperature for at least 547 days. The environmental samples that were protected from direct rain impact exhibited housekeeping and tissue specific mRNA recoverability up to 7 days (saliva and semen), 30 days (blood), or 180 days (vaginal swab). Additionally, rain had a detrimental effect on the recoverability of blood (3 days), saliva (1 day), semen (7 days), and vaginal secretions (3 days) specific transcripts, with one of the mRNA species (the semen marker PRM2) not being detectable after 1 day.

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Year:  2008        PMID: 18298493     DOI: 10.1111/j.1556-4029.2007.00652.x

Source DB:  PubMed          Journal:  J Forensic Sci        ISSN: 0022-1198            Impact factor:   1.832


  24 in total

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2.  The apoptotic thanatotranscriptome associated with the liver of cadavers.

Authors:  Gulnaz T Javan; Ismail Can; Sheree J Finley; Shivani Soni
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Authors:  Bobby L LaRue; Jonathan L King; Bruce Budowle
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4.  Potential forensic application of DNA methylation profiling to body fluid identification.

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Journal:  Int J Legal Med       Date:  2011-04-06       Impact factor: 2.686

5.  mRNA profiling using a minimum of five mRNA markers per body fluid and a novel scoring method for body fluid identification.

Authors:  Amy D Roeder; Cordula Haas
Journal:  Int J Legal Med       Date:  2012-12-20       Impact factor: 2.686

6.  A 17-month time course study of human RNA and DNA degradation in body fluids under dry and humid environmental conditions.

Authors:  Miriam Sirker; Peter M Schneider; Iva Gomes
Journal:  Int J Legal Med       Date:  2016-05-16       Impact factor: 2.686

7.  Evaluation of the inclusion of circular RNAs in mRNA profiling in forensic body fluid identification.

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Journal:  Int J Legal Med       Date:  2017-09-25       Impact factor: 2.686

8.  Comprehensive examination of conventional and innovative body fluid identification approaches and DNA profiling of laundered blood- and saliva-stained pieces of cloths.

Authors:  G Kulstein; P Wiegand
Journal:  Int J Legal Med       Date:  2017-09-29       Impact factor: 2.686

9.  A method for isolating and analyzing human mRNA from newborn stool.

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10.  Dating bloodstains with fluorescence lifetime measurements.

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Journal:  Chemistry       Date:  2012-01-04       Impact factor: 5.236

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