Switching genes to silent mode near DNA double‐strand breaks |
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Authors: | Sophie E Polo |
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Affiliation: | Epigenetics & Cell Fate Centre, UMR7216 CNRS, Sorbonne Paris Cité, Paris Diderot University, Paris, France |
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Abstract: | Transcription is tightly regulated in response to DNA damage. Rapid and transient pausing of RNA polymerase II (RNAPII) is indeed critical to restrict the production of aberrant transcripts from damaged loci and to prevent deleterious collisions between transcription and repair machineries. Yet, how DNA lesions signal to the transcription machinery to coordinate DNA repair with transcriptional silencing is not fully elucidated. In this issue of EMBO Reports, Awwad et al 1 bring a new piece to the puzzle by identifying the negative transcription elongation factor NELF as a critical player in this process. They demonstrate that NELF is recruited to DNA double‐strand breaks (DSBs) near transcriptionally active genes in a poly(ADP‐ribose)‐ and RNAPII‐dependent manner to promote transcriptional repression and facilitate DSB repair. |
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