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| This image shows a sub-fossilized insect in copal (Credit: Dr. David Penney/ University of Manchester) |
The research was conducted wearing full forensic suits in the dedicated ancient DNA facility at The University of Manchester, which comprises a suite of independent, physically isolated laboratories, each with an ultra-filtered air supply maintaining positive displacement pressure and a managed access system.
According to Professor Brown: "In the original 1990s studies DNA amplification was achieved by a process called the polymerase chain reaction (PCR), which will preferentially amplify any modern, undamaged DNA molecules that contaminate an extract of partially degraded ancient ones to give false positive results that might be mistaken for genuine ancient DNA. Our approach, using 'next generation' sequencing methods is ideal for ancient DNA because it provides sequences for all the DNA molecules in an extract, regardless of their length, and is less likely to give preference to contaminating modern molecules."
The team concluded that their inability to detect ancient DNA in relatively young (60 years to 10,600 years old) sub-fossilized insects in copal, despite using sensitive next generation methods, suggests that the potential for DNA survival in resin inclusions is no better, and perhaps worse, than that in air-dried museum insects (from which DNA has been retrieved using similar techniques). This raises significant doubts about claims of DNA extraction from fossil insects in amber, many millions of years older than copal.
Dr Penney said: "Intuitively, one might imagine that the complete and rapid engulfment in resin, resulting in almost instantaneous demise, might promote the preservation of DNA in a resin entombed insect, but this appears not to be the case. So, unfortunately, the Jurassic Park scenario must remain in the realms of fiction."
Source: Manchester University [September 11, 2013]






