Hi all,

I need help in understanding some article.Article is about transcription induced mutations.It is basically about cytosine deamination to thymine during transcription and this mutation(deamination) happens in the coding strand(non trancribing strand).The article says that it doesn’t get repaired by nucleotide excision repair system because the repair system is biased.I need help in understanding the whole paragraph.Please help.Here is the paragraph.

”If separation of DNA strands increases the risk of hydrolytic
deamination, cellular processes such as transcription, replication,
conjugation, and recombination have the potential of
promoting C to T mutations. For example, in a simple model
for transcription elongation, the nontranscribed strand should
be transiently in single-strand form when the transcription
bubble passes through. Such potential deamination risk for
cytosines in the nontranscribed strand during transcription has
been noted before (17–20), but has not been investigated in
depth. A possible reason for this inattention is the existence of
strand bias in nucleotide excision repair. In E. coli (21) and in
mammalian cells (22), transcription-blocking lesions are repaired
preferentially when present in the transcribed strand.
Transcription-coupled nucleotide excision repair has helped
explain the observed bias in mutations caused by mutagens
such as UV light in favor of the nontranscribed strand (23–25),
and has raised the possibility that all observations of strand
bias in mutations may be explained by strand bias in DNA
repair. In fact, Skandalis et al. (19) have argued that there is
a strand bias in 5meC to T mutations in the human hprt gene
and have suggested that this is the result of strand bias in a base
excision repair process that repairs T:G mismatches.”