Defining the RNaseH2 enzyme-initiated ribonucleotide excision repair pathway in Archaea

• Published in: The Journal of biological chemistry 2017-05, Vol.292 (21), p.8835-8845
• Main Authors: Heider, Margaret R., Burkhart, Brett W., Santangelo, Thomas J., Gardner, Andrew F.
• Format: Article
• Language: English
• Subjects: archaea; Archaeal Proteins - genetics; Archaeal Proteins - metabolism; DNA and Chromosomes; DNA Breaks, Single-Stranded; DNA damage; DNA Ligases - genetics; DNA Ligases - metabolism; DNA Polymerase beta - genetics; DNA Polymerase beta - metabolism; DNA repair; DNA Repair - physiology; DNA replication; DNA synthesis; DNA, Archaeal - genetics; DNA, Archaeal - metabolism; enzyme kinetics; pre-steady-state kinetics; Ribonuclease H - genetics; Ribonuclease H - metabolism; ribonucleotide excision repair; RNaseH2; Thermococcus - genetics; Thermococcus - metabolism
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M117.783472

Incorporation of ribonucleotides during DNA replication has severe consequences for genome stability. Although eukaryotes possess a number of redundancies for initiating and completing repair of misincorporated ribonucleotides, archaea such as Thermococcus rely only upon RNaseH2 to initiate the pathway. Because Thermococcus DNA polymerases incorporate as many as 1,000 ribonucleotides per genome, RNaseH2 must be efficient at recognizing and nicking at embedded ribonucleotides to ensure genome integrity. Here, we show that ribonucleotides are incorporated by the hyperthermophilic archaeon Thermococcus kodakarensis both in vitro and in vivo and a robust ribonucleotide excision repair pathway is critical to keeping incorporation levels low in wild-type cells. Using pre-steady-state and steady-state kinetics experiments, we also show that archaeal RNaseH2 rapidly cleaves at embedded ribonucleotides (200-450 s−1), but exhibits an ∼1,000-fold slower turnover rate (0.06–0.17 s−1), suggesting a potential role for RNaseH2 in protecting or marking nicked sites for further processing. We found that following RNaseH2 cleavage, the combined activities of polymerase B (PolB), flap endonuclease (Fen1), and DNA ligase are required to complete ribonucleotide processing. PolB formed a ribonucleotide-containing flap by strand displacement synthesis that was cleaved by Fen1, and DNA ligase sealed the nick for complete repair. Our study reveals conservation of the overall mechanism of ribonucleotide excision repair across domains of life. The lack of redundancies in ribonucleotide repair in archaea perhaps suggests a more ancestral form of ribonucleotide excision repair compared with the eukaryotic pathway.