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DNA polymerase ε harmonizes topological states and R-loops formation to maintain genome integrity in Arabidopsis.


ABSTRACT: Genome topology is tied to R-loop formation and genome stability. However, the regulatory mechanism remains to be elucidated. By establishing a system to sense the connections between R-loops and genome topology states, we show that inhibiting DNA topoisomerase 1 (TOP1i) triggers the global increase of R-loops (called topoR-loops) and DNA damages, which are exacerbated in the DNA damage repair-compromised mutant atm. A suppressor screen identifies a mutation in POL2A, the catalytic subunit of DNA polymerase ε, rescuing the TOP1i-induced topoR-loop accumulation and genome instability in atm. Importantly we find that a highly conserved junction domain between the exonuclease and polymerase domains in POL2A is required for modulating topoR-loops near DNA replication origins and facilitating faithful DNA replication. Our results suggest that DNA replication acts in concert with genome topological states to fine-tune R-loops and thereby maintain genome integrity, revealing a likely conserved regulatory mechanism of TOP1i resistance in chemotherapy for ATM-deficient cancers.

SUBMITTER: Li Q 

PROVIDER: S-EPMC10682485 | biostudies-literature | 2023 Nov

REPOSITORIES: biostudies-literature

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DNA polymerase ε harmonizes topological states and R-loops formation to maintain genome integrity in Arabidopsis.

Li Qin Q   Zhou Jincong J   Li Shuai S   Zhang Weifeng W   Du Yingxue Y   Li Kuan K   Wang Yingxiang Y   Sun Qianwen Q  

Nature communications 20231127 1


Genome topology is tied to R-loop formation and genome stability. However, the regulatory mechanism remains to be elucidated. By establishing a system to sense the connections between R-loops and genome topology states, we show that inhibiting DNA topoisomerase 1 (TOP1i) triggers the global increase of R-loops (called topoR-loops) and DNA damages, which are exacerbated in the DNA damage repair-compromised mutant atm. A suppressor screen identifies a mutation in POL2A, the catalytic subunit of DN  ...[more]

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