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Quantification
and presence of human ancient DNA in burial place
remains of Turkey using real time
polymerase chain reaction
Hasibe Cingilli Vural
Selcuk
University, Science Faculty, Department of Molecular
Biology, Turkey.
E-mail:
hcvural@gmail.com.
Abbreviations: aDNA, ancient DNA; nDNA,
nuclear DNA; RT-PCR, real time-polymerase chain
reaction.
Accepted
29 June, 2009 |
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Archaeometry and forensic laboratories are increasingly
confronted with problematic samples from the scene of
samples, containing only minute amounts of deoxyribonucleic
acid (DNA), which may include polymerase chain reaction (PCR)
inhibiting substances. Efficient DNA extraction procedures,
as well as accurate DNA quantification methods, are critical
steps involved in the process of successful DNA analysis of
such samples. Genomic DNA was extracted automatically by
using EZ1 Automatic Nucleic Acid Isolation System (Qiagen,
Germany) with investigator kit (Qiagen, Ilden, Germany) from
ancient bones. This method is a sensitive for the extraction
of DNA from a wide variety of forensic samples, although it
is known to be laborious compared with single tube
extraction methods. The relatively high DNA recovery and the
quality of the extracted DNA speak for itself. For reliable
and sensitive DNA quantitation, the application of real time
PCR is described. A published real-time PCR assay, which
allows for the combined analysis of nuclear or ancient DNA
and mitochondrial DNA, was modified.
This approach can be used for recovering DNA from the
surface of fossil bone remains in Turkey via a simple
procedure that permits a direct quantitative and qualitative
assessment of molecular markers. Using quantitative RT-PCR,
the
available sources of total aDNA was shown to consists of
intact DNA that is virtually free of RNA, resulting in a
more accurate representation of gene expression using RT-PCR
and PCR amplification methods. In this study, the results
demonstrate that RT-PCR method can be useful for the
improved ancient DNA extraction in anthropology and
archeology.
Key
words:
Ancient DNA, fossil bone, RT-PCR. |