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Mol Cell Biol. 1989 February; 9(2): 421-429

A cysteine-rich nuclear protein activates yeast metallothionein gene transcription.

M S Szczypka and D J Thiele

Department of Biological Chemistry, University of Michigan Medical School, Ann Arbor 48109-0606.

ABSTRACT

The ACE1 gene of the yeast Saccharomyces cerevisiae is required for copper-inducible transcription of the metallothionein gene (CUP1). The sequence of the cloned ACE1 gene predicted an open reading frame for translation of a 225-amino-acid polypeptide. This polypeptide was characterized by an amino-terminal half rich in cysteine residues and positively charged amino acids. The arrangement of many of the 12 cysteines in the configuration Cys-X-Cys or Cys-X-X-Cys suggested that the ACE1 protein may bind metal ions. The carboxyl-terminal half of the ACE1 protein was devoid of cysteines but was highly acidic in nature. The ability of a bifunctional ACE1-beta-galactosidase fusion protein to accumulate in yeast cell nuclei was consistent with the possibility that ACE1 plays a direct role in the regulation of copper-inducible transcription of the yeast metallothionein gene.


Mol Cell Biol. 1989 February; 9(2): 421-429




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