Abstract
A series of BAL31 deletions were constructed in vitro in the upstream region of the Saccharomyces cerevisiae CYC7 gene, encoding the iso-2-cytochrome c protein. These deletions identified two sites which play a role in governing the expression of this gene. A positive site, the deletion of which led to decreased CYC7 expression, lay ca. 240 base pairs 5' to the translational initiation codon (-240). A negative site, the deletion of which led to greatly increased levels of CYC7 expression, lay at ca. -300 bp. Deletion of both these sites resulted in low wild-type-like expression of the gene. Therefore, these two sites appear to act antagonistically to give the low wild-type levels of CYC7 expression. Within the region defined as containing the positive site, there is a sequence which bears some homology to the upstream activation sites in the regulated gene, CYC1, encoding the iso-1-cytochrome c protein.
MeSH Terms
Base Sequence
Chromosome Deletion
DNA Restriction Enzymes/metabolism
Deoxyribonuclease BamHI
Deoxyribonucleases, Type II Site-Specific
Gene Expression Regulation
Plasmids
Saccharomyces cerevisiae/genetics
Chemicals
DNA Restriction Enzymes
Deoxyribonuclease BamHI
CTCGAG-specific type II deoxyribonucleases
CTGCAG-specific type II deoxyribonucleases
Deoxyribonucleases, Type II Site-Specific
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Wright C F
Zitomer R S
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