Profiling DNA damage and repair capacity in sea urchin larvae and coelomocytes exposed to genotoxicants

Helena C. Reinardy, Andrea G. Bodnar

Research output: Contribution to journalArticle

15 Citations (Scopus)

Abstract

The ability to protect the genome from harmful DNA damage is critical for maintaining genome stability and protecting against disease, including cancer. Many echinoderms, including sea urchins, are noted for the lack of neoplastic disease, but there are few studies investigating susceptibility to DNA damage and capacity for DNA repair in these animals. In this study, DNA damage was induced in adult sea urchin coelomocytes and larvae by exposure to a variety of genotoxicants [UV-C (0-3000 J/m2), hydrogen peroxide (0-10 mM), bleomycin (0-300 μM) and methylmethanesulfonate (MMS, 0-30 mM)] and the capacity for repair was measured over a 24-h period of recovery. Larvae were more sensitive than coelomocytes, with higher levels of initial DNA damage (fast micromethod) for all genotoxicants except MMS and increased levels of mortality 24 h following treatment for all genotoxicants. The larvae that survived were able to efficiently repair damage within 24-h recovery. The ability to repair DNA damage differed depending on treatments, but both larvae and coelomocytes were able to most efficiently repair H2O2-induced damage. Time profiles of expression of a panel of DNA repair genes (ddb1, ercc1, xpc, xrcc1, pcna, ogg1, parp1, parp2, ape, brca1, rad51, xrcc2, xrcc3, xrcc4, xrcc5, xrcc6 and gadd45), throughout the period of recovery, showed greater gene induction in coelomocytes compared with larvae, with particularly high expression of xrcc1, ercc1, parp2 and pcna. The heterogeneous response of larvae to DNA damage may reflect a strategy whereby a subset of the population is equipped to withstand acute genotoxic stress, while the ability of coelomocytes to resist and repair DNA damage confirm their significant role in protection against disease. Consideration of DNA repair capacity is critical for understanding effects of genotoxicants on organisms, in addition to shedding light on life strategies and disease susceptibility.

Original languageEnglish
Pages (from-to)829-839
Number of pages11
JournalMutagenesis
Volume30
Issue number6
DOIs
Publication statusPublished - 14 Jul 2015

Keywords

  • bleomycin
  • adult
  • dna damamge
  • dna repair
  • genes
  • hydrogen peroxide
  • larva
  • proliferating cell nuclear antigen
  • sea urchins
  • mortality
  • dna repair gene
  • ercc1 gene
  • xrdd1 gene

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