Table 1.
Damage | Type of process | Effects on DNA molecule | Possible solutions in aDNA classical sequencing methodologies |
---|---|---|---|
Oxidative damage |
Formation of strand breaks (single-stranded nicks) |
Cleavage of the phosphodiester backbone |
PCR of overlapping fragments of short length |
Depurination resulting in a baseless site |
Multiple independent PCR Cloning and sequencing of several clones |
||
Breakage of the sugar backbone through b-elimination |
Uracil-N-glycolase treatment |
||
Results in lesions blocking the polymerase enzyme, and promoting chimeric sequences through ‘jumping’ PCR |
Blocking primers Single primer extension or Spex |
||
Degradation by microorganisms’ nucleases in the post mortem cell |
Strand breaks |
Short fragment length |
PCR of overlapping fragments of short length |
DNA crosslinks |
Inter-strand crosslinks by alkylation |
May prevent the amplification of endogenous template molecules |
PTB (N-phenylacyl thiazolium bromide) |
|
Intermolecular crosslinks by Maillard reaction |
Increases the risk of contamination |
|
Hydrolysis damage | Results in miscoding lesions, for example, deamination of cytosine and adenine to uracil and hypoxathine, respectively | Results in the incorporation of erroneous bases during amplification and change of coding | Multiple independent PCR Cloning and sequencing of several clones UNG treatment |
UNG : Uracil-N-glycosylase; Spex: Single Primer Extension; PTB: N-phenylacyl thiazolium bromide.