Yeast Sen1 Helicase Protects the Genome from Transcription-Associated Instability

Hannah E. Mischo(University of Oxford), Belén Gómez‐González(Centro Andaluz de Biología Molecular y Medicina Regenerativa), Pawel Grzechnik(University of Oxford), Ana G. Rondón(University of Oxford), Wu Wei(European Molecular Biology Laboratory), Lars M. Steinmetz(European Molecular Biology Laboratory), Andrés Aguilera(Centro Andaluz de Biología Molecular y Medicina Regenerativa), Nick J. Proudfoot(University of Oxford)
Molecular Cell
January 1, 2011
Cited by 349Open Access
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Abstract

Sen1 of S. cerevisiae is a known component of the NRD complex implicated in transcription termination of nonpolyadenylated as well as some polyadenylated RNA polymerase II transcripts. We now show that Sen1 helicase possesses a wider function by restricting the occurrence of RNA:DNA hybrids that may naturally form during transcription, when nascent RNA hybridizes to DNA prior to its packaging into RNA protein complexes. These hybrids displace the nontranscribed strand and create R loop structures. Loss of Sen1 results in transient R loop accumulation and so elicits transcription-associated recombination. SEN1 genetically interacts with DNA repair genes, suggesting that R loop resolution requires proteins involved in homologous recombination. Based on these findings, we propose that R loop formation is a frequent event during transcription and a key function of Sen1 is to prevent their accumulation and associated genome instability.


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