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Nucleic Acids Research logoLink to Nucleic Acids Research
. 1998 Dec 1;26(23):5441–5447. doi: 10.1093/nar/26.23.5441

Dehydromonocrotaline generates sequence-selective N-7 guanine alkylation and heat and alkali stable multiple fragment DNA crosslinks.

T N Pereira 1, R I Webb 1, P E Reilly 1, A A Seawright 1, A S Prakash 1
PMCID: PMC147994  PMID: 9826770

Abstract

Monocrotaline is a pyrrolizidine alkaloid known to cause toxicity in humans and animals. Its mechanism of biological action is still unclear although DNA crosslinking has been suggested to a play a role in its activity. In this study we found that an active metabolite of monocrotaline, dehydromonocrotaline (DHM), alkylates guanines at the N7 position of DNA with a preference for 5'-GG and 5'-GA sequences. In addition, it generates piperidine- and heat-resistant multiple DNA crosslinks, as confirmed by electrophoresis and electron microscopy. On the basis of these findings, we propose that DHM undergoes rapid polymerization to a structure which is able to crosslink several fragments of DNA.

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