How to Prevent DNA Degradation in Urine Samples?
DNA in urine degrades rapidly, which hinders its application in individual identification. How can we prevent DNA degradation in urine and improve its value in forensics?
Urine contains urea, uric acid, creatine, mineral salts, urokinase and other substances that facilitate DNA degradation. Bacteria in urine also break down DNA. Additionally, PCR inhibitors in urine like β-hCG lower DNA extraction efficiency.
Most studies store urine samples at low temperatures to prevent DNA degradation. However, low temperature also causes precipitation of crystals in urine, forming sandy sediments that interfere with DNA extraction. So cooling alone cannot completely prevent DNA degradation.
UTI (urinary trypsin inhibitor) is a drug that specifically inhibits pancreatic enzymes and is used to treat pancreatitis etc. Studies show that adding UTI to urine samples inhibits protease degradation of DNA and enhances DNA stability. Appropriate UTI can keep urinary DNA detectable for longer.
Tris-EDTA in urine can chelate cations like calcium and magnesium, acting as a decalcifying agent to reduce precipitation of urate salts and calcium oxalate and avoid their interference with DNA extraction. Additionally, Tris-EDTA increases urine pH which inhibits uric acid crystals formed under acidic conditions. Thus, appropriate Tris-EDTA also improves DNA extraction efficiency.
Higher salt content in large urine volumes interferes with extracting DNA from urine. Research indicates that dividing samples into small batches and then pooling DNA extracts increases recovery rate and provides more complete microbial profiles.
In summary, to improve urinary DNA stability, appropriate UTI or Tris-EDTA can be added promptly after sample collection followed by low temperature storage; and dividing samples into small batches during DNA extraction avoids excess salts and improves DNA extraction efficiency from urine. This holds significance for further individual identification studies on urine.
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