Dynamic Regulation of Copper Uptake and Detoxification Genes in Saccharomyces cerevisiae

ABSTRACT

The essential yet toxic nature of copper demands tight regulation of the copper homeostatic machinery to ensure that sufficient copper is present in the cell to drive essential biochemical processes yet prevent the accumulation to toxic levels. In Saccharomyces cerevisiae, the nutritional copper sensor Mac1p regulates the copper-dependent expression of the high affinity Cu(I) uptake genesCTR1, CTR3, and FRE1, while the toxic copper sensor Ace1p regulates the transcriptional activation of the detoxification genes CUP1, CRS5, and SOD1 in response to copper. In this study, we characterized the tandem regulation of the copper uptake and detoxification pathways in response to the chronic presence of elevated concentrations of copper ions in the growth medium. Upon addition of CuSO₄, mRNA levels of CTR3 were rapidly reduced to eightfold the original basal level whereas the Ace1p-mediated transcriptional activation of CUP1 was rapid and potent but transient.CUP1 expression driven by an Ace1p DNA binding domain-herpes simplex virus VP16 transactivation domain fusion was also transient, demonstrating that this mode of regulation occurs via modulation of the Ace1p copper-activated DNA binding domain. In vivo dimethyl sulfate footprinting analysis of the CUP1 promoter demonstrated transient occupation of the metal response elements by Ace1p which paralleled CUP1 mRNA expression. Analysis of a Mac1p mutant, refractile for copper-dependent repression of the Cu(I) transport genes, showed an aberrant pattern of CUP1expression and copper sensitivity. These studies (i) demonstrate that the nutritional and toxic copper metalloregulatory transcription factors Mac1p and Ace1p must sense and respond to copper ions in a dynamic fashion to appropriately regulate copper ion homeostasis and (ii) establish the requirement for a wild-type Mac1p for survival in the presence of toxic copper levels.

ACKNOWLEDGMENTS

We thank the members of the Thiele laboratory for stimulating discussions and critical comments. We are grateful to Simon Labbéfor providing plasmids pSKCUP1, pSKCTR3, ura3::KanMX2, and pKSACT1 and to Zhiwu Zhu for providing plasmids pRSMAC1(HA) and pRSMAC1^up1(HA).

This work was supported by National Institutes of Health (NIH) grant RO1 GM41840 to D.J.T., postdoctoral fellowship-National Research Service Award F32 GM18089 from NIH to M.M.O.P., and Cellular Biotechnology Training Program NIH grant GM08353 to K.A.K. D.J.T. is a Burroughs Wellcome Toxicology Scholar.