The Smc5/6 complex counteracts R-loop formation at highly transcribed genes in cooperation with RNase H2

The R-loop is a common transcriptional by-product that consists of an
RNA-DNA duplex joined to a displaced strand of genomic DNA. While the
effects of R-loops on health and disease are well established, there is
still an incomplete understanding of the cellular processes responsible
for their removal from eukaryotic genomes. Here, we show that a core
regulator of chromosome architecture —the Smc5/6 complex— plays a crucial
role in the degradation of R-loop structures formed during gene
transcription. Consistent with this, mutants defective in the Smc5/6
complex and enzymes involved in R-loop resolution show strong synthetic
interactions and accumulate high levels of RNA-DNA hybrid structures in
their chromosomes. Importantly, we demonstrate that the Smc5/6 complex
recognizes specific types of RNA-DNA hybrid structures in vivo and
promotes the degradation of R-loops by RNase H enzymes. Collectively, our
results reveal a crucial role for the Smc5/6 complex in the removal of
toxic R-loops formed at highly transcribed genes and telomeres.