An alternative pathway for repair of deaminated bases in DNA triggered by archaeal NucS endonuclease

Likui Zhang (1) , Haoqiang Shi (1) , Qi Gan (1) , Yuxiao Wang , Mai Wu (1) , Zhihui Yang (2) , Philippe M. Oger (3, 4) , Jianting Zheng

1 Yangzhou University
2 Agricultural University of Hebei
3 MAP - Microbiologie, adaptation et pathogénie
4 M2E - Microbiology of Extreme Environments

Recent studies show that NucS endonucleases participate in mismatch repair in several archaea and bacteria. However, the function of archaeal NucS endonucleases has not been completely clarified. Here, we describe a NucS endonuclease from the hyperthermophilic and radioresistant archaeon Thermococcus gammatolerans (Tga NucS) that can cleave uracil (U)-and hypoxanthine (I)-containing dsDNA at 80°C. Biochemical evidence shows that the cleavage sites of the enzyme are at the second phosphodiester on the 5′-site of U or I, and at the third phosphodiester on the 5′-site of the opposite base of U or I, creating a double strand break with a 4-nt 5′-overhang.The ends of the cleaved product of Tga NucS are ligatable, possessing 5′-phosphate and 3′-hydroxyl termini, which can be utilized by DNA repair proteins or enzymes. Tga NucS displays a preference for U/G-and I/T-containing dsDNA over other pairs with U or I, suggesting that the enzyme is responsible for repair of U and I in DNA that arise from deamination. Biochemical characterization of cleaving U-and I-containing DNA by Tga NucS was also investigated. The DNA-binding results show that the enzyme exhibits a higher affinity for normal, U-and I-containing dsDNA than for normal, U-and I-containing ssDNA. Therefore, we present an alternative pathway for repair of deaminated bases in DNA triggered by archaeal NucS endonuclease in hyperthermophilic archaea.

Domaines: Biochimie [q-bio.BM]; Biologie moléculaire

Likui Zhang, Haoqiang Shi, Qi Gan, Yuxiao Wang, Mai Wu, et al.. An alternative pathway for repair of deaminated bases in DNA triggered by archaeal NucS endonuclease. DNA Repair, 2020, pp.102734. ⟨10.1016/j.dnarep.2019.102734⟩. ⟨hal-02334467⟩