The Mig1p repressor from the food yeast Candida utilis has been isolated us
ing a homologous PCR hybridization probe. This probe was amplified with two
sets of degenerate primers designed on the basis of highly conserved motif
s in the DNA-binding region (zinc-finger domain) from yeast Mig1p and fungi
CreA repressors. The cloned gene was sequenced and found to encode a polyp
eptide of 345 amino acids which shows significant identity with other yeast
and fungus repressors in the DNA-binding domain and also with the yeast Mi
g1 proteins in the C-terminal region (effector domain). The MIG1 repressor
gene from C. utilis was able to complement functionally the mig1 mutation o
f S. cerevisiae. The sequence presented here has been deposited in the EMBL
data library under Accession No. AJ277830. Copyright (C) 2001 John Wiley &
Sons, Ltd.