Copper Differentially Regulates the Activity and Degradation of Yeast Mac1 Transcription Factor*

Copper is an essential metal ion that is toxic when accumulated to high intracellular concentrations. The yeast Mac1 protein is a copper-sensing transcription factor that is essential for both the activation and inactivation of genes required for high affinity copper ion transport. Here we demonstrate that in response to low copper ion concentrations Mac1 protein is rendered inactive for copper transporter gene transcription. Under high copper ion concentrations Mac1 is degraded in a rapid, copper-specific manner. This degradation is critical to prevent copper toxicity that would otherwise result from sustained expression of the copper transport genes. These results demonstrate that nutritional and toxic copper concentrations elicit distinct fates for the Mac1 copper-sensing transcription factor and establish a new mechanism by which trace metals regulate gene expression.

[1]  D. Kosman,et al.  Homeostatic Regulation of Copper Uptake in Yeast via Direct Binding of MAC1 Protein to Upstream Regulatory Sequences ofFRE1 and CTR1 * , 1997, The Journal of Biological Chemistry.

[2]  D. Thiele,et al.  Copper-specific Transcriptional Repression of Yeast Genes Encoding Critical Components in the Copper Transport Pathway* , 1997, The Journal of Biological Chemistry.

[3]  D. Winge,et al.  Copper-mediated repression of the activation domain in the yeast Mac1p transcription factor. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[4]  D. Alexandraki,et al.  The Yeast Fre1p/Fre2p Cupric Reductases Facilitate Copper Uptake and Are Regulated by the Copper-modulated Mac1p Activator* , 1997, The Journal of Biological Chemistry.

[5]  D. Thiele,et al.  A widespread transposable element masks expression of a yeast copper transport gene. , 1996, Genes & development.

[6]  J. Bonifacino,et al.  Copper‐dependent degradation of the Saccharomyces cerevisiae plasma membrane copper transporter Ctr1p in the apparent absence of endocytosis. , 1996, The EMBO journal.

[7]  R J Fletterick,et al.  Delocalizing trypsin specificity with metal activation. , 1996, Biochemistry.

[8]  D. Thiele,et al.  Autoactivation by a Candida glabrata copper metalloregulatory transcription factor requires critical minor groove interactions , 1996, Molecular and cellular biology.

[9]  S. Merchant,et al.  Degradation of Plastocyanin in Copper-deficient Chlamydomonas reinhardtii , 1995, The Journal of Biological Chemistry.

[10]  R. Hassett,et al.  Evidence for Cu(II) Reduction as a Component of Copper Uptake by Saccharomyces cerevisiae(*) , 1995, The Journal of Biological Chemistry.

[11]  R. Klausner,et al.  Molecular characterization of a second iron-responsive element binding protein, iron regulatory protein 2. Structure, function, and post-translational regulation. , 1994, The Journal of biological chemistry.

[12]  G. Fink,et al.  Regulated degradation of the transcription factor Gcn4. , 1994, The EMBO journal.

[13]  W. Howard,et al.  CRS5 encodes a metallothionein-like protein in Saccharomyces cerevisiae. , 1994, The Journal of biological chemistry.

[14]  J. Rine,et al.  Regulated degradation of HMG-CoA reductase, an integral membrane protein of the endoplasmic reticulum, in yeast , 1994, The Journal of cell biology.

[15]  R. Klausner,et al.  Molecular characterization of a copper transport protein in S. cerevisiae: An unexpected role for copper in iron transport , 1994, Cell.

[16]  J. Jungmann,et al.  MAC1, a nuclear regulatory protein related to Cu‐dependent transcription factors is involved in Cu/Fe utilization and stress resistance in yeast. , 1993, The EMBO journal.

[17]  K. Karlin Metalloenzymes, structural motifs, and inorganic models. , 1993, Science.

[18]  D. Thiele,et al.  ACE1, a copper-dependent transcription factor, activates expression of the yeast copper, zinc superoxide dismutase gene. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[19]  P. Sorger,et al.  Yeast heat shock factor is an essential DNA-binding protein that exhibits temperature-dependent phosphorylation , 1988, Cell.

[20]  D. Thiele ACE1 regulates expression of the Saccharomyces cerevisiae metallothionein gene , 1988, Molecular and cellular biology.

[21]  B. Halliwell,et al.  Oxygen toxicity, oxygen radicals, transition metals and disease. , 1984, The Biochemical journal.