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Topoisomerase I suppresses genomic instability by preventing interference between replication and transcription.


ABSTRACT: Topoisomerase I (Top1) is a key enzyme in functioning at the interface between DNA replication, transcription and mRNA maturation. Here, we show that Top1 suppresses genomic instability in mammalian cells by preventing a conflict between transcription and DNA replication. Using DNA combing and ChIP (chromatin immunoprecipitation)-on-chip, we found that Top1-deficient cells accumulate stalled replication forks and chromosome breaks in S phase, and that breaks occur preferentially at gene-rich regions of the genome. Notably, these phenotypes were suppressed by preventing the formation of RNA-DNA hybrids (R-loops) during transcription. Moreover, these defects could be mimicked by depletion of the splicing factor ASF/SF2 (alternative splicing factor/splicing factor 2), which interacts functionally with Top1. Taken together, these data indicate that Top1 prevents replication fork collapse by suppressing the formation of R-loops in an ASF/SF2-dependent manner. We propose that interference between replication and transcription represents a major source of spontaneous replication stress, which could drive genomic instability during the early stages of tumorigenesis.

SUBMITTER: Tuduri S 

PROVIDER: S-EPMC2912930 | biostudies-literature | 2009 Nov

REPOSITORIES: biostudies-literature

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Topoisomerase I suppresses genomic instability by preventing interference between replication and transcription.

Tuduri Sandie S   Crabbé Laure L   Conti Chiara C   Tourrière Hélène H   Holtgreve-Grez Heidi H   Jauch Anna A   Pantesco Véronique V   De Vos John J   Thomas Aubin A   Theillet Charles C   Pommier Yves Y   Tazi Jamal J   Coquelle Arnaud A   Pasero Philippe P  

Nature cell biology 20091018 11


Topoisomerase I (Top1) is a key enzyme in functioning at the interface between DNA replication, transcription and mRNA maturation. Here, we show that Top1 suppresses genomic instability in mammalian cells by preventing a conflict between transcription and DNA replication. Using DNA combing and ChIP (chromatin immunoprecipitation)-on-chip, we found that Top1-deficient cells accumulate stalled replication forks and chromosome breaks in S phase, and that breaks occur preferentially at gene-rich reg  ...[more]

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