bioRxivMolecular BiologyPreprint
Rapid delivery of RNase H1 enables replication fork progression under stress independently of R-loop resolution
Amandine Basille, Yi‐Ching LiniD, Connor KirkeiD, David CluetiD, Yara Bawadi, Laetitia VacheziD, Virgile Dervieux, Laura Guiguettaz, Pascal BernardiD, Stephan HamperliD, Philippe PaseroiD, Emiliano P. RicciiD, Vincent VanoosthuyseiD
Abstract
The over-expression of RNase H1 enables the progression of replication forks under stress and safeguards genome stability. The most common interpretation of these observations is that RNase H1 over-expression removes R-loops, whose formation would hinder replication fork progression. Here we challenge this model using an innovative strategy to rapidly deliver ready-made Escherichia coli RNase H1 (RnhA) in live cells. We show that RnhA is enriched in the vicinity of active replication forks and that it rescues replication fork progression in different stress conditions. However, RnhA had no impact on R-loops mapped by the DRIP or Cut&Tag methods. Our results reveal the existence of distinct populations of RNA:DNA hybrids that are differently sensitive to RnhA and invites new interpretations of well-established observations. HIGHLIGHTSO_LIRapid delivery of R-loop sensors and regulators in live cells C_LIO_LIRapid delivery of RnhA rescues replication fork progression in stress conditions C_LIO_LIRapid delivery of RnhA does not impact R-loops C_LIO_LIDRIP detects RNA:DNA species insensitive to RNase H1 in cells C_LI
- organism: E. coli
- assay: DNA methylation
- assay: ChIP-seq
- research focus: cell type annotation
- research focus: differential expression
- research focus: gene regulatory network inference
- research focus: cell-cell communication
- approach: experimental assay
- Citations
- 0
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