A putative stimulatory role for activator turnover in gene expression
Abstract
The ubiquitin–proteasome system (UPS) promotes the destruction of target proteins by attaching to them a ubiquitin chain that is recognized by the 26S proteasome. The UPS influences most cellular processes, and its targets include transcriptional activators that are primary determinants of gene expression. Emerging evidence indicates that non-proteolytic functions of the UPS might stimulate transcriptional activity. Here we show that the proteolysis of some transcriptional activators by the UPS can stimulate their function. We focused on the role of UPS-dependent proteolysis in the function of inducible transcriptional activators in yeast, and found that inhibition of the proteasome reduced transcription of the targets of the activators Gcn4, Gal4 and Ino2/4. In addition, mutations in SCF^(Cdc4), the ubiquitin ligase for Gcn4 (ref. 5), or mutations in ubiquitin that prevent degradation, also impaired the transcription of Gcn4 targets. These transcriptional defects were manifested despite the enhanced abundance of Gcn4 on cognate promoters. Proteasome inhibition also decreased the association of RNA polymerase II with Gcn4, Gal4 and Ino2/4 targets, as did mutations in SCFCdc4 for Gcn4 targets. Expression of a stable phospho-site mutant of Gcn4 (ref. 7) or disruption of the kinases that target Gcn4 for turnover alleviated the sensitivity of Gcn4 activity to defects in the UPS.
Additional Information
© 2005 Nature Publishing Group. Received 2 June 2005; Accepted 3 August 2005. We thank D. Finley, D. H. Wolf, R. Young, A. Hinnebusch, J. Shaw, B. Westermann, J. Nunnari and G. Braus for gifts of strains and reagents; B. Tansey for communicating results before publication; and J. Shaw, B. Westermann, J. Nunnari, S. Sadis, A. Ansari and the members of the Deshaies laboratory for comments and criticism. This work was supported in part by an NIH Research Project Grant to R.J.D. R.J.D. is an Investigator of the Howard Hughes Medical Institute. J.R.L. was supported by an NIH National Research Service Award and a Caltech-Amgen Postdoctoral Fellowship.Attached Files
Published - nature04098-s2.pdf
Supplemental Material - nature04098-s1.doc
Supplemental Material - nature04098-s3.pdf
Supplemental Material - nature04098-s4.pdf
Supplemental Material - nature04098-s5.pdf
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Additional details
- Eprint ID
- 56069
- Resolver ID
- CaltechAUTHORS:20150325-103747797
- NIH
- Howard Hughes Medical Institute (HHMI)
- Caltech-Amgen Postdoctoral Fellowship
- Created
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2015-03-25Created from EPrint's datestamp field
- Updated
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2021-11-10Created from EPrint's last_modified field