Buccal cells DNA extraction to obtain high quality human genomic DNA suitable for polymorphism genotyping by PCR-RFLP and Real-Time PCR

ORIGINAL ARTICLES

Buccal cells DNA extraction to obtain high quality human genomic DNA suitable for polymorphism genotyping by PCR-RFLP and Real-Time PCR

Erika Calvano Küchler^I; Patricia Nivoloni Tannure^II; Priscila Falagan-Lotsch^III; Taliria Silva Lopes^IV; Jose Mauro Granjeiro^{III, V, VI}; Lidia Maria Fonte Amorim^VI

^IPhD, Molecular Biology Laboratory, Cell Therapy Center, Unit of Clinical Research, University Hospital Antonio Pedro, Fluminense Federal University (UFF), Niteroi, RJ, Brazil

^IIPhD, Department of Pediatric Dentistry and Orthodontics, Federal University of Rio de Janeiro (UFRJ); Discipline of Pediatric Dentistry, School of Dentistry, Veiga de Almeida University (UVA), Rio de Janeiro, Brazil

^IIIPhD, Molecular Biology Laboratory, Cell Therapy Center, Unit of Clinical Research, University Hospital Antonio Pedro, Fluminense Federal University (UFF), Niteroi, RJ, Brazil

^IVMSc student, Molecular Biology Laboratory, Cell Therapy Center, Unit of Clinical Research, University Hospital Antonio Pedro, Fluminense Federal University (UFF), Niteroi, RJ, Brazil

^VPhD, Senior Researcher, Bioengineering Program, National Institute of Standardization, Quality and Technology (Inmetro). Duque de Caxias, RJ, Brazil

^VIPhD, Associate Professor, Department of Molecular and Cellular Biology, Federal Fluminense University (UFF), Niteroi, RJ, Brazil

^{Corresponding address}

ABSTRACT

OBJECTIVE: The aim of this study was to evaluate, by PCR-RFLP and real-time PCR, the yield and quality of genomic DNA collected from buccal cells by mouthwash after different storage times at room temperature.

MATERIAL AND METHODS: A group of volunteers was recruited to collect buccal cells using a mouthwash solution. The collected solution was divided into 3 tubes, one tube were used for immediate extraction and the remaining received ethanol and were kept at room temperature for 4 and 8 days followed by dna extraction. The concentration, purity and integrity of the dna were determined using spectrophotometry and electrophoresis. DNA quality differences among the three incubation times were also evaluated for genotyping EGF +61 a/g (rs 4444903) polymorphism by PCR-RFLP and for IRF6 polymorphism (rs 17015215) using real-time PCR.

RESULTS: There was no significant difference of dna yield (p=0.75) and purity (p=0.86) among the three different incubation times. DNA obtained from different incubation times presented high-molecular weight. The PCR-RFLP and real time pcr reactions were successfully performed for all DNA samples, even those extracted after 8 days of incubation. All samples genotyped by real-time pcr presented c allele for irf6 gene polymorphism (homozygous: cc; heterozygous: Ct) and the C allele was used as a reference for Ct values. The samples presented the same genotype for the different times in both techniques.

CONCLUSION: We demonstrated that the method described herein is simple and low cost, and that DNA can be extracted and pcr amplified after storage in mouthwash solution at room temperature.

Key words: DNA. Saliva. PCR. Genetic polymorphism.

INTRODUCTION

In the last years, the advances in molecular genetics research provided substantial progress regarding the identification of genes involved in the pathogenesis of human alterations and diseases². Molecular epidemiological studies regarding the association of mutation/polymorphisms with orofacial diseases, including oral clefts, developmental dental alterations and oral diseases (i.e. caries lesion and periodontal disease), advanced on many levels^14,19,20.

In epidemiological studies¹⁰, most of them using polymerase chain reaction (PCR) technique¹⁷, obtaining high-quality genomic DNA is critical. In most cases the preferred source of material is peripheral blood. Blood sampling, however, may be problematic in cases such as extreme illness or elderly people, babies and people that are reluctant to be submitted to this invasive procedure. For this reason, buccal cell collection is gaining recognition as an alternative specimen source for DNA isolation in clinical and research testing⁶. Additionally, clinical validation studies have shown that DNA diagnostic results from patient-matched buccal cells and whole blood are comparable³.

Buccal cells can be obtained for DNA isolation using mouthwashes, cytobrushes, swabs, treated cards and whole saliva collection. Mulot, et al.¹² (2005) compared cytology brushes, mouthwash and treated cards for DNA collection and concluded that cytobrush appears to be the most appropriate method with good quality and high security in multicenter studies. On the other hand, another study comparing oral rinse, cytobrush and swab using Oragene^® DNA collection kit to extract DNA showed that oral rinse provided sufficient DNA quantity and quality better than the buccal swab and brush techniques¹⁶.

Commercially available DNA isolation kits are produced mainly in industrialized countries, and may not be readily available at affordable prices in developing and underdeveloped countries¹. In order to establish DNA collection of a large number of samples for epidemiological studies, we used a simple and cost-efficient protocol^1,7. The aim of this study was to evaluate, by restriction fragment length polymorphism-PCR (PCR-RFLP) and Real-time PCR, the yield and quality of genomic DNA collected from buccal cells by mouthwash after different storage times at room temperature.

MATERIAL AND METHODS

A group of 12 volunteers of both genders (with ages ranging from 20 to 54 years) were enrolled to collect buccal cells using a mouthwash solution. Ethical approval was obtained from the Human Ethics Committee of the Health Department of the city of Rio de Janeiro, Rio de Janeiro, Brazil (113/09). Informed consent was obtained from all participating individuals. The individuals were instructed to brush their teeth or rinse the mouth with water for at least 2 h prior to saliva collection.

Saliva collection

Buccal cells were collected by rinsing the mouth for 60 s with 15 mL of saline and expectorating the rinse in a 50 mL propylene tube. In order to assess the DNA integrity over time, the mouthwash solution was divided into 3 tubes.

One tube was used for immediate extraction (T0) and the two remaining received ethanol up to a 70% final concentration and were kept at room temperature for 4 (T4) or 8 (T8) days followed by DNA isolation.

DNA extraction

Genomic DNA was extracted from buccal epithelial cells following a modified protocol reported by Aidar and Line¹ (2007). Briefly, after incubation the tubes were centrifuged for 10 min at 550 xg at room temperature to pellet the bucal cells. The supernatant was discarded and 1 mL of extraction solution (Tris-HCl 10 mM, pH 7.8; EDTA 5 mM; SDS 0.5 %) containing proteinase K (100 ng/mL) (Invitrogen, Grand Island, NY, USA) was added to cause lysis of cells and proteins. After overnight incubation the non-digested proteins were removed by adding 400 μL of 10 M ammonium acetate. The solutions were mixed by gently reversing the tube 20 times and centrifuged at 12,000 xg for 15 min. Supernatant was separated into two clean 1.5 mL microtubes (700 μL) and DNA was precipitated with 700 μL of isopropanol at -20°C for 30 minutes. After centrifugation for 20 min at 12,000 xg at 4°C, the supernatant was poured off and the pellet washed with 1 mL of 70 % ethanol. Ethanol was decanted carefully after centrifugation at 12,000 xg for 15 min at 4°C, the tubes were reversed and allowed to air-dry during 45 to 60 min on an absorbent paper. DNA was resuspended in 100 μL of TE buffer (10 mM Tris (pH 7.8) and 1 mM EDTA) and stored at -20°C.

Criteria for evaluating DNA extraction after different incubation times

1. Concentration measurement assays

The concentration and purity of the DNA was determined by spectrophotometry using NanoDrop 2000c. DNA concentration was evaluated at 260 nm and the ratio of readings at 260 nm and 280 nm was used to estimate the DNA purity.

2. DNA integrity

The integrity of genomic DNA for 0, 4- and 8-day incubation times was assessed by resolving DNA on a 0.8 % agarose gel by electrophoresis, followed by visualization with ethidium bromide staining.

3- DNA quality and polymorphism genotyping.

PCR Assays and RFLP

In order to evaluate DNA quality for polymorphism genotyping by PCR-RFLP DNA samples of each incubation time were assayed as previously described by Shahbazi¹⁸ (2002), for the polymorphism in the EGF (+61 A/G) gene. The PCR reaction was carried out in a 30 µL mixture containing 160 ng of genomic DNA, 1x Dream Taq Buffer (Fermentas, Maryland, NY, USA), 0.2 mM of dNTPs (Fermentas), 0.3 µM of each primer (Forward: 5' TGTCACTAAAGGAAAGGAGG3'; Reverse: 5' TTCACAGAGTTTAACAGCCC 3' - Invitrogen, Grand Island, NY, USA) and 1 U Dream Taq DNA Polymerase (Fermentas, Maryland, NY, USA). The cycling conditions comprised an initial denaturation step for 10 min at 96°C, followed by 44 cycles consisting of three steps: 96°C for 30 sec, 61°C for 30 sec and 72°C for 1 min. A final extension step was performed at 72°C for 10 min.

The amplified fragment (242 bp) was digested with 2 U of Alu I (New England Biolabs, Beverly, MA, USA) at 37°C overnight, electrophoresed on a 2.5% agarose gel stained with ethidium bromide and photographed under UV illumination. Four fragments (15, 34, 91 and 102 bp) were produced in the presence of A allele and three fragments (15, 34 and 193 bp) were produced in the presence of G allele. In the gel, the 15 and 39 bp fragments were not visible. Therefore, the G allele was differentiated from the A allele by visualization of a single 193 bp fragment instead of the 91 and 102 bp fragments.

TaqMan amplification

DNA quality differences among the three incubation times were also evaluated by Real-Time PCR. The cycle threshold (Ct) is defined as the number of cycles required for the fluorescent signal to cross the threshold. In a real time PCR assay a positive reaction is detected by accumulation of a fluorescent signal. Ct levels are inversely proportional to the amount of target nucleic acid in the sample.

Quantified DNA was diluted to 4 ng/mL and 6 ng of DNA were used to perform the genotyping of IRF6 polymorphism (C/T transition, rs 17015215) using Taqman probes¹⁵ in an Sequence Detection System instrument (Mx3005P system; Stratagene). Assays and reagents were supplied by Applied Biosystems (Foster City, CA, USA). Determination of amplification was computed as a Ct value using the MxPro-Mx3005p software supplied by the manufacturer.

Statistical analysis

Comparisons of the three incubation times were made to determine differences in mean total DNA yield and PCR and Real-Time amplification Ct under different sample storage times were tested using ANOVA.

RESULTS

The total DNA yield measured at 260 nm was 19.4±8.4 µg (11.1 - 38.8 µg), 24.2±13.9 µg (9.0 - 51.5 µg) and 21.9±13.8 µg (9.3 - 46.4 µg) and the mean OD 260/280 ratio was 2.03±0.04 (1.97-2.12), 2.01±0.05 (1.94-2.05) and 2.02±0.09 (1.87-2.15) for T0, T4 and T8 respectively.

This results indicated that there was no significant difference between the three different incubation times for DNA yield (p=0.75) and purity (p=0.86).

Gel electrophoresis was used to visualize the presence of high-molecular weight DNA. DNA obtained from different incubation times presented high-molecular weight for all three times (Figure 1).

The PCR-RFLP-reactions were successfully performed for all DNA samples, even using DNA samples extracted after 8-day incubation time. Four different samples representing PCR products and genotyping by restriction enzymes are illustrated in Figure 2.

All samples were also successfully genotyped by Real-Time PCR using TaqMan probes. All of them presented C allele for IRF6 gene polymorphism (homozygous - CC and heterozygous - CT) and the C allele was used as a reference for Ct values. The Ct values ranged from 26 to 28 and the Ct mean values are presented on Figure 3B for T0, T4 and T8 incubation times. There is no difference between mean Ct values and incubation time (p=0.73) (Figure 3B).

The samples presented the same genotype after the different times for both techniques.

DISCUSSION

Exfoliated buccal epithelial cells in saliva are a very promising alternative source of DNA because they can be obtained using self-administered, noninvasive, and relatively inexpensive techniques^5,10,13. Collection of samples for DNA extraction is a critical procedure as it is time-consuming and may involve ethical aspects. It is, therefore, desirable that this procedure becomes more simple and low-cost¹. The protocol proposed here has some advantages, for being simple, low cost and not using phenol-chloroform as in other techniques^11,16,21. Our results showed that the buccal cells provided satisfactory amount of DNA. Our mouthwash method presented similar values from other mouthwash methods^6,8. In our sample, the amount of extracted DNA had inter-individual variation depending on the buccal mucosa.

Previous studies reported the greatest similar efficiency values for mouthwash and cytobrush, based on the same DNA extraction method^4,8. However, saline mouthwash has lower cost when compared with cytobrush.

DNA quality can be affected by the collection method (primary integrity and protein contamination) and by the isolation method (integrity and protein, organic, salt and alcohol contamination)¹⁶. In our study, the mean OD 260/280 ratio was 2.02, indicating that in most cases the bulk of proteins were successfully removed by ammonium acetate precipitation.

The storage time at room temperature had few effects on DNA stability at room temperature. This could be crucial for large-scale epidemiological studies, which require a time for collection logistics. On the other hand, the main purpose of collecting DNA is for future studies and our RFLP-PCR and Real-Time PCR was successfully performed for the three incubation times.

CONCLUSION

Our results demonstrated that the method described here is low-cost and simple to be performed by dental and medical researchers. DNA can be extracted and PCR amplified after storage in mouthwash solution at room temperature. Several samples can be processed at the same time and the extracted DNA yields sufficient material for many genetic studies.

ACKNOWLEDGMENTS

This study was supported in part by grants from the Nacional Council for Scientific and Technological Development (CNPq grant 482457/2009-0) and the Rio de Janeiro Research Foundation (FAPERJ grant E-26/102.729/2008).

Received: November 11, 2010

Modification: September 17, 2011

Accepted: September 30, 2011

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Publication Dates

• Publication in this collection
  27 Sept 2012
• Date of issue
  Aug 2012

History

• Received
  11 Nov 2010
• Accepted
  30 Sept 2011
• Reviewed
  17 Sept 2011