Purpose of Experiment Use miRNA in forensic applications by recovering miRNA from samples obtained for forensics and identifying the bodily fluid it came from. Prove that miRNA assaying can be cheaper, easier, and overall capable in forensic labs. (http://www.kenoshapolice.com/UserFiles/image/crime%20scene.jpg)
Forensic Background Forensic investigations often involve body fluids, such as blood and saliva These fluids contain mRNAs and more stable miRNAs Fluids can connect suspects to crime scenes or victims and miRNAs is easier and faster than other methods (http://www.leelofland.com/wordpress/wp-content/uploads/2011/07/New-Picture-67.jpg)
Micro-RNA Background Small noncoding RNA Used in cellular processes, posttranslational miRNA regulation used for controlling gene expression. Binds to mRNA (http://cnx.org/content/m36053/latest/mirna.png)
Experiment: Step 1 Fluids were obtained through buccal swabs for saliva and vacutainer tubes for blood. The microarray method used fluids from 4 females and 1 male Verification by PCR used samples from 3 females and 2 males Aged blood was made from one sample over one year (http://anotherstudentdoctor.files.wordpress.com/2010/09/vacutainer.jpg) (http://www.dnares.in/images/header/buccal-swab-collection.jpg)
Experiment: Step 2 Extraction of RNA from all samples Enriched for miRNAs with kits Buffer used to remove erythrocytes from blood RNA concentration was found using RNA integrity number (RIN) from fluorometer and bioanalyzer
Experiment: Step 3 Microarrays were used Probes were created as reverse complements of miRNAs from known human sequences Positive results for blood and saliva were selected for from respective arrays http://www.biolab.cn/uploads/1/Image/20090606110818709.gif
Experiment: Step 4 RT-PCR was done on each selected sample for both blood and saliva From before, miRNA was extracted again cDNA was created by reverse transcriptase after polyadenylation by poly (A) polymerase Oligo-dT primers were used to tag the 5’ end for quantitative PCR
FIG. 5—Expression of candidate miRNAs in different kinds of tissue. Upper panel: Normalized median expression of the three blood-miRNAs (miR-126, miR-150, miR-451) in blood, saliva, liver, muscle and brain Lower panel: Normalized median expression of the three saliva-miRNAs (miR-200c, miR-203, miR-205) in blood, saliva, liver, muscle and brain. FIG. 4—qPCR validation of candidate miRNAs for blood and saliva. Upper panel: relative expression of blood candidate miRNAs in blood compared to saliva, for which expression has been arbitrarily set to 0; Central panel: relative expression of blood candidate miRNAs in aged blood compared to saliva for which expression has been arbitrarily set to 0; Lower panel: relative expression of saliva candidate miRNAs in saliva compared to blood for which expression has been arbitrarily set to 0.
Results As seen previously, 3 candidates from both blood and saliva contained specific miRNAs Aged blood also resulted in miRNA assay, proving that miRNA could withstand some degradation A mixed sample of blood and saliva resulted in distinguishing between the two types of samples
Future Applications Hopefully, widespread use in forensic labs Standardization of the procedure for validation and optimal processes for distinction More research into other body fluids, such as semen, vaginal secretions, and menstrual blood Use especially in rape cases http://www.fresnosheriff.org/images/Forensic-Lab-Technologist.jpg
References Courts, C; Madea, B. “Specific micro-RNA signatures for the detection of saliva and blood in forensic body-fluid identification.” J Forensic Sci. v.56 no. 6 p. 1464-1470. 2011. Landgraf, P; Rusu, M; Sheridan, R; et al. “A mammalian microRNA expression atlas based on small RNA library sequencing.” Cell. v. 129 no. 7 p. 1401–14. 2007.
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