Identification of Molecular Biomarkers for Estimation of Postmortem Interval Using Blood Samples – A Pilot Study
Hyeyoung Lee, Ji-Young Lee, Sunghyun Kim, Yeonim Choi,Yeun kim, Kiyoon Eom
BDetermination of the postmortem interval (PMI) is a major focus of investigation in forensic science. A panel of physical methods, such as the measurement of body temperature or the electrical stimulation of facial muscles, allows initial determination of PMI with considerable accuracy . However, accurate PMI estimation still remains difficult due to many intrinsic factors such as age, sex, and physiological and pathological states of the deceased, as well as extrinsic factors such as temperature, humidity, and insect activity . All methods presently used to estimate the time of death are affected by some degree of inaccuracy. These methods only provide an approximation since several variables including environmental temperature, body structure, cause of death, location of the body, or putative drug consumption can influence the rate of post mortem changes. In recent years, analysis of the biochemical changes in certain markers, such as glucose and electrolytes, for PMI estimation has made significant progress [3,4]. However, detection of postmortem changes in protein, RNA, and DNA markers has not yet been systematically studied. Several studies have tried to determine changes in molecular markers to provide more useful information regarding PMI [5-7]. In general, mRNA is thought to be much less stable than DNA and protein. However, there are several reports that suggest the contrary. RNA degradation in the body after death might be a useful marker for the precise estimation of PMI .
The aim of this study was to characterize the expression and degradation levels of RNA markers, including human 18S rRNA and several mRNAs of housekeeping genes including β-actin (ACTB), β2-microglobulin (B2M), peptidylprolyl isomerase A (PPIA), β-glucuronidase (GUSB), hypoxanthine-guanine phosphoribosyl transferase (HPRT1), phosphoglycerate kinase 1 (PGK1), 60S acidic ribosomal protein P0 (RPLPO), TATA-binding protein (TBP), and transferrin receptor protein 1(TFRC), in whole blood samples after collection at different time points and temperature conditions (at 4°C and 25°C). The gathered information was then used for estimation of an accurate PMI. Real-time reverse transcription polymerase chain reaction (RT-PCR) TaqMan assay was used to detect changes in RNA markers.
Materials and Methods
This study was performed at Yonsei University in Wonju, Republic of Korea, from December 2013 to April 2014. Whole blood samples were collected using EDTA blood collection tubes. All participants provided written informed consent. The Institutional Ethics Committee of Yonsei University Wonju Campus approved the study (approval number 1041849- 201406-BM-025-02). A total of six samples of EDTA whole blood from study participants were incubated for nine different time points (none, 6 hr, 1, 3, 5, 10, 15, 20, and 30 days) at two temperature conditions, 25°C and 4°C. After incubation, blood samples were harvested and stabilized in RNAgard Blood tubes (Biometrica Inc., San Diego, CA, USA) and stored at -20°C before total RNA preparation.
Total RNA extraction
Next, 2.5 mL of stabilized blood samples were transferred to 50 mL conical tubes, to which 3 mL of Precipitation Buffer was added. The mixture was then incubated at room temperature on a shaking incubator for 30 minutes and centrifuged at room temperature for 30 minutes at 9,000 x g. The supernatant was then decanted, and 350 μL of Resuspension Buffer was added to the pellet and resuspended. To this solution, 250 μL of 100% ethanol was added and centrifuged for 1 minute at 8,000 x g. Next, 400 μL of Wash Buffer 1 was added and centrifuged at 8,000 x g for 1 minute, followed by addition of 100 μL of DNaseⅠMix and incubation at room temperature for 20 minutes. The solution was then treated with 400 μL of Wash Buffer 1 and centrifuged at 8,000 x g for 1 minute. To the pellet, 350 μL of Wash Buffer 2 was added, centrifuged at 8,000 x g for 1 minute (repeat twice), and then centrifuged at 11,000 x g for 2 minutes to dry the pellet. Next, 50 μL of RNase-free water was added, incubated for 1 minute at room temperature and centrifuged for 1 minute at 8,000 x g to elute RNA. The contents and purity of RNA were measured at 260 nm and 280 nm, using a Nanodrop spectrophotometer, InfiniteⓇ 200 Pro NanoQuant (Tecan, Mannedorf, Switzland).
RNA quality analysis
RNA integrity and degradation levels were assessed using an automated chip-based microfluidic capillary electrophoretic separation system, 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA, USA), and the Agilent RNA 6000 Nano Kit (Agilent Technologies) according to the manufacturer’s instructions. Results were analyzed using Agilent 2100 Expert software v.B.02.07.SI532 (Agilent Technologies).
Gene Expression Analysis
The RT-qPCR TaqMan® assay was carried out on an ABI 7500 Fast system (Applied Biosystems, Foster City, CA, USA) for thermal cycling and fluorescence detection, according to manufacturer instructions. PCR primers and corresponding TaqMan®probes were designed (IDT, Coralville, IA, USA) for 11 different human 18S rRNA and housekeeping gene mRNA of ACTB, B2M, PPIA, GUSB, HPRTI, PGK1, RPLPO, TBP, GAPDH and TFRC (Table 1). For real-time thermal cycling, 500 ng/ uL of cDNA and THUNDERBIDR® Probe qPCR Mix (Toyobo, Osaka, Japan) was used. After initial denaturation at 95°C for 3 min, the PCR for DNA detection was run for 40 cycles (15 sec at 95°C, 1 min at 55°C) using an ABI 7500 fast system (ABI, Carlsbad, California, USA). The threshold cycle (Ct) value for each reaction was automatically calculated and recorded using the 7500 software v2.0.6.
Statistical analysis was performed using Microsoft® Office Excel v. 2010 (Microsoft, Redmond, Washington, USA).
Time-dependent changes in RNA integrity
RNA integrity number (RIN) was measured using an automated microfluidic chip system, and RIN values ranged from 1 to 10, where 1 represents totally degraded RNA and 10 represents completely intact RNA . A shift toward shorter fragment sizes is observed with progressing degradation. It was obvious that band patterns of 18S and 28S rRNA were clear until three days after blood collection at both temperatures, at 4°C and 25°C. However, the band patterns of 18S and 28S rRNA gradually faded after ten days, and RIN values were unmeasurable (Figure 1 and Table 2).
Time-dependent changes in RNA markers according to RT-qPCR
In order to determine the usefulness of RNA markers to estimate PMI, time-dependent changes in 11 RNA markers in
Figure 2. Detection limits of the three target probes in ten-fold serial diluted blood samples.
Table 2. RNA integrity number (RIN) of for each sample as an indication of RNA integrity, the 18S/28S ratio, and an estimation of concentration. blood samples were analyzed using RT-qPCR targeting ACTB, B2M, GAPDH, PGK1, GUSB, HPRT1, PPIA, RPLPO, TBP, and TFRC mRNAs and 18S rRNA.
As shown in Figure 2, all RNA markers were degraded slower at 4°C than at 25°C. The mRNA levels of GADPH, B2M, and HPRT1 at 25°C and GAPDH at 4°C were maintained at a relatively constant level for three days. After five days, the mRNA levels of those markers gradually decreased. 18S rRNA and mRNA levels of ACTB, PPIA, GUSB, PGK1, RPLPO, TBP, and TFRC were not remarkably changed at either temperature.
This study investigated RNA markers for estimating PMI from blood samples. Blood samples are easily obtained from living persons and thus can be used for methodical evaluation. However, blood samples pose several problems when using RT-qPCR because the aspects involved in estimating PMI are much more complicated in the scene of incident than in experimental conditions.
In the present study, to overcome the limitations of previous PMI estimation approaches, the integrity of 18S and 28S rRNA and mRNA levels of ten housekeeping genes were analyzed. Analysis methods included microfluidic electrophoresis chip and RT-qPCR TaqMan assays over nine different time points (0, 6 hr, 1, 3, 5, 10, 15, 20, 30 days) and two temperature conditions, at 4°C and 25°C.
Microfluidic electrophoresis results from this study show that PCR bands of 18S and 28S rRNA were maintained for 15 days at 4°C, and 18s rRNA and mRNA levels of all mRNA markers were detected using real-time RT-PCR through 30 days at 4°C and 25°C. In contrast to DNA, RNA is generally believed to be rapidly degraded after death and in vitro due to ubiquitous ribonuclease activity. Many studies, however, reported rather high RNA stability in certain organs such as brain tissues [10- 14]. Results from the present study show that all RNA markers were gradually decreased in a time-dependent manner; however, RNA levels were able to be detected through 30 days after blood collection. Thus, these results were concordant with previous studies regarding RNA in brain tissues .
This study confirmed that levels of certain RNA markers such as 18S rRNA and HPRT1, B2M, and GAPDH mRNAs at 25°C and GAPDH mRNA at 4°C are significantly decreased in a time-dependent manner through 30 days after blood collection, indicating the useful of these markers to estimate PMI even if a dead body is left for several days at variable temperatures. These RNA markers may be affected by released intracellular substances such as enzymes and proteins from hemolysis of red blood cells in whole blood.
In conclusion, we hypothesized that the RNA degradation level in various blood specimens could be measured quantitatively and used as an indicator of PMI for up to 30 days post mortem. We expect that further study using PMI estimation will add valuable information.
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