Genome-wide ribonucleotide detection in Archaea
Yann Moalic1, Maurane Reveil1, Deepali L Kundnani2
1Univ Brest, Ifremer, BEEP, F-29280 Plouzané, France.
Abstract:
Genome integrity is constantly challenged by the incorporation of ribonucleotides ribonucleoside monophosphates (rNMPs) during DNA synthesis. Covalently linked single and several consecutive rNMPs occur in the genome of a number of organisms. They are mainly introduced by DNA polymerases during DNA replication and repair. In general, cells evolved ribonucleases H (RNases H) specialized in the removal of rNMPs from DNA to avoid any detrimental consequences on genome stability. Here, we describe the involvement of types 1 and/or 2 RNases H in processing embedded rNMPs in the genome of two archaeal species Haloferax volcanii and Thermococcus barophilus. Genome-wide, nucleotide-resolution maps of embedded rNMPs reveal oriC-centered strand-switching profiles in H. volcanii ΔrnhB, indicating origin firing in native cells, while their absence in T. barophilus reflects low origin usage. The data also define archaeal sequence-context rules for rNMP embedment, confirm the predominant role of RNase HII in rNMP removal with evidence of compensatory repair pathways, and link incorporation patterns to measured rNTP/dNTP pools. Together, these findings uncover archaeal-specific mechanisms of rNMP incorporation and repair with implications for replication and genome stability.
Insights
Cells incorporate ribonucleotides (rNMPs) into DNA, challenging genome stability. Archaeal Ribonucleases H (RNases H) remove these rNMPs, revealing specific repair pathways and replication insights.
Area of Science:
- Molecular Biology
- Genomics
- Biochemistry
Background:
- Genome integrity is threatened by ribonucleotide monophosphate (rNMP) incorporation during DNA synthesis.
- Ribonucleases H (RNases H) are crucial enzymes for removing rNMPs from DNA to maintain genome stability.
Purpose of the Study:
- Investigate the role of RNase H types 1 and 2 in processing embedded rNMPs in archaea.
- Characterize archaeal mechanisms of rNMP incorporation and repair.
Main Methods:
- Genome-wide nucleotide-resolution mapping of embedded rNMPs.
- Analysis of rNMP profiles in wild-type and mutant archaeal strains (Haloferax volcanii, Thermococcus barophilus).
Main Results:
- Identified strand-switching profiles in H. volcanii ΔrnhB, indicating DNA replication origins.
- Defined archaeal sequence-context rules for rNMP embedment.
- Confirmed RNase HII as the primary enzyme for rNMP removal, with evidence of compensatory repair.
Conclusions:
- Uncovered archaeal-specific mechanisms for rNMP incorporation and repair.
- Demonstrated the link between rNMP incorporation patterns and cellular nucleotide pools.
- Highlighted the implications for DNA replication and genome stability in archaea.
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