UV irradiation induces a non-coding RNA that functionally opposes the protein encoded by the same gene
journal contributionposted on 2020-10-15, 16:41 authored by Laura Williamson, Marco Saponaro, Stefan Boeing, Philip East, Richard Mitter, Theodoros Kantidakis, Gavin P Kelly, Anna Lobley, Jane Walker, Bradley Spencer-Dene, Michael Howell, Aengus Stewart, Jesper Q Svejstrup
The transcription-related DNA damage response was analyzed on a genome-wide scale with great spatial and temporal resolution. Upon UV irradiation, a slowdown of transcript elongation and restriction of gene activity to the promoter-proximal ∼25 kb is observed. This is associated with a shift from expression of long mRNAs to shorter isoforms, incorporating alternative last exons (ALEs) that are more proximal to the transcription start site. Notably, this includes a shift from a protein-coding ASCC3 mRNA to a shorter ALE isoform of which the RNA, rather than an encoded protein, is critical for the eventual recovery of transcription. The non-coding ASCC3 isoform counteracts the function of the protein-coding isoform, indicating crosstalk between them. Thus, the ASCC3 gene expresses both coding and non-coding transcript isoforms with opposite effects on transcription recovery after UV-induced DNA damage.
ASCC3DNA damage responseRNA polymerase IIUV-irradiationalternative last exon splicinglncRNAnon-coding RNAtranscript elongationAlternative SplicingCell LineDNA HelicasesExonsHumansRNA Polymerase IIRNA, MessengerRNA, UntranslatedTranscription Elongation, GeneticTranscription Initiation, GeneticTranscription, GeneticUltraviolet RaysSvejstrup FC001166CBHPHTSAS-ackCS-ackDevelopmental Biology06 Biological Sciences11 Medical and Health Sciences