RNA polymerase II degradation in response to rapamycin is not mediated through ubiquitylation.

Biochem Biophys Res Commun

University of Montreal, Maisonneuve-Rosemont Hospital, Research Center, 5415 de l'Assomption, Montreal, Quebec, Canada H1T 2M4.

Published: September 2011

In Saccharomyces cerevisiae, the immunosuppressor rapamycin engenders the degradation of excessive RNA polymerase II leading to growth arrest but the regulation of this process is not known yet. Here, we show that this mechanism is dependent on the peptidyl prolyl cis/trans isomerase Rrd1. Strikingly this degradation is independent of RNA polymerase II polyubiquitylation and does not require the elongation factor Elc1. Our data reveal that there are at least two alternative pathways to degrade RNA polymerase II that depend on different type of stresses.

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http://dx.doi.org/10.1016/j.bbrc.2011.08.079DOI Listing

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