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Zap1 activation domain 1 and its role in controlling gene expression in response to cellular zinc status
Author(s) -
Herbig Andrew,
Bird Amanda J.,
Swierczek Sabina,
McCall Keith,
Mooney Michelle,
Wu ChangYi,
Winge Dennis R.,
Eide David J.
Publication year - 2005
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1111/j.1365-2958.2005.04734.x
Subject(s) - biology , gene , gene expression , genetics , regulation of gene expression , microbiology and biotechnology , computational biology
Summary The Zap1 transcription factor is a central player in zinc homeostasis in yeast. This protein regulates the expression of genes involved in zinc accumulation and storage. For most of its target genes, Zap1 activates expression in zinc‐limited cells and this function is inhibited in replete cells. Zap1 has two activation domains, AD1 and AD2, which are independently regulated by zinc status. In this study, we characterized AD1 and its regulation by zinc. AD1 was mapped using deletions to residues 332–402 of Zap1. The region required for the zinc responsiveness of this activation domain, designated ‘ZRD AD1 , was mapped to residues 182–502. Thus, AD1 is embedded within its larger zinc‐responsive domain. Using a combination of in silico analysis, random mutagenesis and site‐directed mutagenesis, we identified key residues within ZRD AD1 required for its regulation by zinc. Most of these residues are cysteines and histidines that could potentially serve as Zn(II) ligands. These results suggest that ZRD AD1 senses zinc by direct Zn(II) binding. Consistent with this hypothesis, purified ZRD AD1 bound multiple Zn(II) ions. Finally, our results indicate that, in the context of the full‐length Zap1 protein, AD1 and AD2 are both critical to the full control of gene expression in response to zinc.