Effects of nucleases on cell-free extrachromosomal circular DNA

Cell-free extrachromosomal circular DNA (eccDNA) as a distinct topological form from linear DNA has recently gained increasing research interest, with possible clinical applications as a class of biomarkers. In this study, we aimed to explore the relationship between nucleases and eccDNA characteristics in plasma. By using knockout mouse models with deficiencies in deoxyribonuclease 1 (DNASE1) or deoxyribonuclease 1 like 3 (DNASE1L3), we found that cell-free eccDNA in Dnase1l3(-/-) mice exhibited larger size distributions than that in wild-type mice. Such size alterations were not found in tissue eccDNA of either Dnase1(-/-) or Dnase1l3(-/-) mice, suggesting that DNASE1L3 could digest eccDNA extracellularly but did not seem to affect intracellular eccDNA. Using a mouse pregnancy model, we observed that in Dnase1l3(-/-) mice pregnant with Dnase1l3(+/-) fetuses, the eccDNA in the maternal plasma was shorter compared with that of Dnase1l3(-/-) mice carrying Dnase1l3(-/-) fetuses, highlighting the systemic effects of circulating fetal DNASE1L3 degrading the maternal eccDNA extracellularly. Furthermore, plasma eccDNA in patients with DNASE1L3 mutations also exhibited longer size distributions than that in healthy controls. Taken together, this study provided a hitherto missing link between nuclease activity and the biological manifestations of eccDNA in plasma, paving the way for future biomarker development of this special form of DNA molecules.

Automated summary

This study investigates the relationship between nucleases and extrachromosomal circular DNA (eccDNA) characteristics in plasma. The results show that DNASE1L3 can digest extracellular eccDNA but does not seem to affect intracellular eccDNA. The study also highlights the systemic effects of circulating fetal DNASE1L3 in degrading maternal eccDNA. Patients with DNASE1L3 mutations exhibit longer size distributions of plasma eccDNA compared to healthy controls. Overall, this study provides a missing link between nuclease activity and the biological manifestations of eccDNA in plasma, laying the foundation for future biomarker development.