A simple mouthwash method for genomic DNA isolation in molecular studies

Khor, G. H.; Zain, R.B.; Hassan, M.I. Abu; Ahmed, R.; Khan, Hbsg; Younis, L.T. (2009) A simple mouthwash method for genomic DNA isolation in molecular studies. Oral Oncology, 45 (7). p. 221. ISSN 1368-8375

[img]
Preview
PDF [error in script]
Download (42Kb) | Preview
    [img]
    Preview
    PDF [error in script]
    Download (39Kb) | Preview

      Abstract

      Background: Application of PCR techniques requiring only minute amounts of Genomic DNA. Thus, a less invasive, simpler to perform, and cheaper method to obtain DNA from exfoliated cells is desirable. We aim to develop a method that can obtain high quality of genomic DNA from one sample that allows for numerous application of PCR analysis. Objective: This study describes a simple, inexpensive and non invasive protocol to isolate a high quality of genomic DNA from exfoliated cells by using swish method. Methodology: Twenty two subjects vigorously swished 10 ml of normal saline in their mouth for 60 s and spitted into a collection tube. DNA extraction assay was performed by using saliva DNA isolation kit (Norgen, USA). The washed pellets were suspended in TE buffer and analyzed for the quality and purity of DNA content by using the NanoDrop Spectrophotometer. A ratio of A260/A280 was calculated. The extracted genomic DNA was amplified with primers of p53 intron 6 by using PCR machine. The presence of amplified DNA was then confirmed by electrophoreses analysis, which DNA bands were scanned by Typhoon 9410 variable imager. Results: In this study, the extracted genomic DNA demonstrated an average value of 1.94 O.D. in DNA content purity and 42.9 \ensuremathμg/\ensuremathμl in DNA yields. The electrophoresis images of the DNA products showed visible and detectable bands of higher molecular weight DNA in all the samples. Conclusion: The results showed that the extracted genomic DNA from the exfoliated cells by applying the swish method, that provides substantially larger amounts and higher molecular weight of DNA for down-stream DNA identification application. In addition, all samples were successfully genotyped by PCR-based assays for p53 gene intron 6 regions, which confirmed that the quality of isolated DNA was reliable in supporting the PCR amplification for the molecular studies.

      Item Type: Article
      Creators:
      1. Khor, G. H.
      2. Zain, R.B.
      3. Hassan, M.I. Abu
      4. Ahmed, R.
      5. Khan, Hbsg
      6. Younis, L.T.
      Journal or Publication Title: Oral Oncology
      Additional Information: Prof. Dr. Rosnah Mohd Zain Department of Oral Pathology and Oral Medicine and Periodontology, Faculty of Dentistry, University of Malaya
      Uncontrolled Keywords: Oral squamous cell carcinoma, OSCC, lichenoid lesions, lichen planus, oral cancer, oral tumours, pemphigus, traumatic eosinophilic granuloma, aphthous ulcers, oral mucosal lesions, betel chewers mucosa, betel quid related lesions, betel quid, areca quid, tobacco quid, oral cancer screening, training and calibration, early detection, oral cancer awareness, biobanking, tissue bank, databank, oral cancer, tissue bank, research credibility, research ethics.
      Subjects: R Medicine > RK Dentistry
      R Medicine > RK Dentistry > Oral surger
      Divisions: Faculty of Dentistry > Dept of Oral Pathology & Oral Medicine & Periodontology
      Depositing User: Prof. Dr. Rosnah Mohd Zain
      Date Deposited: 09 Jan 2012 10:52
      Last Modified: 09 Jan 2012 10:52
      URI: http://eprints.um.edu.my/id/eprint/2408

      Actions (For repository staff only: Login required)

      View Item

      Document Downloads

      More statistics for this item...