Nucleic Acids Research Advance Access published online on February 5, 2008
Nucleic Acids Research, doi:10.1093/nar/gkn005
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The 3' processing factor CstF functions in the DNA repair response
1Chemistry Department, Hunter College, City University of New York and 2Department of Biological Sciences, Columbia University, New York, NY 10027, USA
*To whom correspondence should be addressed. Tel: +1 212 772 5355; Fax: +1 212 772 5332; Email: fkleiman{at}hunter.cuny.edu
Received September 10, 2007. Revised January 7, 2008. Accepted January 7, 2008.
Following DNA damage, mRNA levels decrease, reflecting a coordinated interaction of the DNA repair, transcription and RNA processing machineries. In this study, we provide evidence that transcription and polyadenylation of mRNA precursors are both affected in vivo by UV treatment. We next show that the polyadenylation factor CstF, plays a direct role in the DNA damage response. Cells with reduced levels of CstF display decreased viability following UV treatment, reduced ability to ubiquitinate RNA polymerase II (RNAP II), and defects in repair of DNA damage. Furthermore, we show that CstF, RNAP II and BARD1 are all found at sites of repaired DNA. Our results indicate that CstF plays an active role in the response to DNA damage, providing a link between transcription-coupled RNA processing and DNA repair.
The authors wish it to be known that, in their opinion, the first two authors should be regarded as joint First Authors.