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http://www.scirp.org/journal/PaperInformation.aspx?PaperID=52307#.VI-oXsnQrzE
Author(s)
In today’s research driven society, it has become
commonplace for institutions to rely upon DNA and RNA extraction
techniques to help obtain genomic data from old specimens. Generally,
specimens are preserved for future gross examination and/or teaching.
Using histological examination of specimens from museum jars from the
Pathology Department at the Indiana University School of Medicine, the
sequential and chronological degradation of DNA and RNA has been
studied. We examined gross specimens from 1920 to 2000. We evaluated
histologic preservation of kidney, liver, heart, lung, spleen, uterus
and brain for nuclear structure in these samples. Nuclear preservation
was based on amount of nuclei per microscopic field and the crispness of
the nuclear membrane and internal features. The nuclei in high lipid
tissues such as the brain were found to degrade at a quicker rate than
dense tissues such as the heart and uterus. Our study has shown that
specimens preserved beyond fifty years were likely to have little to no
nuclei left, thus indicating that there was little to no DNA and RNA
remaining. This technique of histologic evaluation is an important
finding and a general guideline which may save research institutions
from the expensive process of DNA and RNA extraction.
KEYWORDS
Cite this paper
Cook, S. , Dodge, C. , Morgan, R. and Sandusky, G.
(2015) DNA/RNA Degradation Rate in Long Term Fixed Museum Specimens. Forensic Medicine and Anatomy Research, 3, 1-6. doi: 10.4236/fmar.2015.31001.
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