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Department of Legal Medicine, College of Medicine and Odontology, University of Valencia E.G., 46010 Valencia, Spain
1Correspondence: Facultad de Medicina, U. D. Medicina Legal, Av., Blasco Ibañez, no. 15, 46010-Valencia, Spain. E-mail: Fernando.Verdu{at}uv.es
| DNA FROM LIP PRINTS? |
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The possibility of studying profiles of DNA obtained from fingerprints allows us to consider that invisible or latent lip prints (that is, lip prints from protective lipstick or long-lasting lipstick that does not leave any visible mark) may provide cell remains from which DNA can be extracted. The following study demonstrates an attempt to obtain DNA from latent lip prints on porous surfaces (paper handkerchiefs).
When dealing with latent traces, the first step is visualizing them by a developing process.
The developing of latent lip prints on porous surfaces is more recent than that for fingerprints. The first research showed that traditional reagents used for fingerprints are not successful (2)
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It has recently been determined that lysochromes (above all, Sudan Black CI 26150) are quite effective in developing recent latent lip prints, as well as older ones, on porous surfaces (3)
.
Once the print has been detected, a trace is available from which to procure cell remains that can supply enough DNA to be analyzed by the PCR technique.
The aim of our work was to determine whether from a latent lip print developed with Sudan Black it was possible to extract DNA of sufficient quality and amount to be amplified, thereby providing potential usefulness for identification. For this first study, three loci will be amplified. The results can provide important information regarding:
| METHODS |
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Five volunteers (named A, B, C, D, E) collaborated in procuring samples. From each the following samples were obtained:
Development procedure with Sudan Black (powder) (4)![]()
Using a brush, carefully apply a small quantity of powder on the surface in order to locate the latent print. Extend and continue applying until the print can be seen clearly.
DNA extraction
Three-millimeter side squares were cut out from all prints in order to attempt DNA extraction using the Chelex method (5)
. As a control, bucal samples from participating individuals were used.
DNA quantification
The amount and quality of DNA obtained were determined (Biophotometer Eppendorf®) and checked to ascertain whether enough DNA from all samples could be obtained for amplification. Quantities obtained from the different samples can fluctuate between 2 and 16.4 ng/µL. The minimum DNA for amplification recommended is 5 ng (6)
.
DNA amplification
The extracted DNA was typed at the STR loci HUMvWA, FGA, and TH01 following conditions described in the bibliography (6
7
8)
, with a final volume of 25 µL from which 10 µL of DNA extract was obtained. PCR was carried out in an Eppendorf ® Mastercicler. The PCR products obtained were subjected to electrophoresis separation. Amplified alleles were separated by electrophoresis in polyacrylamide gel (7)
. Products were visualized using a silver stain procedure.
| RESULTS |
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| DISCUSSION |
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Despite the difficulties that may arise, the possibility of obtaining DNA from latent prints makes these traces doubly useful for identification: besides the traditional analysis of labial lines, it is possible to get a print makers genetic profile.
In conclusion, the search for invisible or latent prints at a crime scene requires increasingly simpler, more sensitive, and effective methods. It is of paramount importance that the method used permit subsequent analyses. In many cases it can be verified that common reagents in biochemical and medical test methods can be useful for crime investigation. This is why the life sciences are an indispensable tool in criminal justice: they play a fundamental role in developing new methods and improving existing ones.
Received for publication September 25, 2003. Accepted for publication January 7, 2004.
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