Author/Authors :
Manuel J. Mu?oz، نويسنده , , M. Soledad Pérez Santangelo، نويسنده , , Maria P. Paronetto، نويسنده , , Manuel de la Mata، نويسنده , , Federico Pelisch، نويسنده , , Stéphanie Boireau، نويسنده , , Kira Glover-Cutter، نويسنده , , Claudia Ben-Dov، نويسنده , , Mat?as Blaustein، نويسنده , , Juan J. Lozano، نويسنده , , Gregory Bird، نويسنده , , David Bentley، نويسنده , , Edouard Bertrand، نويسنده , , Alberto R. Kornblihtt، نويسنده ,
Abstract :
DNA damage induces apoptosis and many apoptotic genes are regulated via alternative splicing (AS), but little is known about the control mechanisms. Here we show that ultraviolet irradiation (UV) affects cotranscriptional AS in a p53-independent way, through the hyperphosphorylation of RNA polymerase II carboxy-terminal domain (CTD) and a subsequent inhibition of transcriptional elongation, estimated in vivo and in real time. Phosphomimetic CTD mutants not only display lower elongation but also duplicate the UV effect on AS. Consistently, nonphosphorylatable mutants prevent the UV effect. Apoptosis promoted by UV in cells lacking p53 is prevented when the change in AS of the apoptotic gene bcl-x is reverted, confirming the relevance of this mechanism. Splicing-sensitive microarrays revealed a significant overlap of the subsets of genes that have changed AS with UV and those that have reduced expression, suggesting that transcriptional coupling to AS is a key feature of the DNA-damage response.
