Abstract
BUR1, which was previously identified by a selection for mutations that have general effects on transcription in Saccharomyces cerevisiae, encodes a cyclin-dependent kinase that is essential for viability, but none of its substrates have been identified to date. Using an unbiased biochemical approach, we have identified the carboxy-terminal domain (CTD) of Rpb1, the largest subunit of RNA polymerase II, as a Bur1 substrate. Phosphorylation of Rpb1 by Bur1 is likely to be physiologically relevant, sincebur1 mutations interact genetically with rpb1CTD truncations and with mutations in other genes involved in CTD function. Several genetic interactions are presented, implying a role for Bur1 during transcriptional elongation. These results identify Bur1 as a fourth S. cerevisiae CTD kinase and provide striking functional similarities between Bur1 and metazoan P-TEFb.
ACKNOWLEDGMENTS
We thank Fred Winston for critical reading of the manuscript and Gerard Faye, Arno Greenleaf, and David Bregman for reagents and strains.
This work was supported by research grants GM60479 to G.H. and GM52486 to G.P. from the National Institutes of Health.