Abstract
In Saccharomyces cerevisiae, the genes encoding at least 10 enzymes involved in DNA replication are periodically expressed in the late G1 and S phases of the cell cycle. All of these genes have one copy or more of the sequence ACGCGT, which conforms to the recognition site for the Mlu I restriction endonuclease. For the CDC21, CDC9, and POL1 genes, the Mlu I site has been shown to be absolutely required for periodic transcription. Using nuclear extracts fractionated by conventional and oligonucleotide affinity chromatography, we have purified a 17-kDa protein that recognizes the Mlu I motif. Synthetic oligonucleotides containing mutated Mlu I sites do not bind the protein. In contrast, synthetic oligonucleotides derived from the CDC2, CDC6, and CDC21 genes, which are expressed with the same timing as POL1, bind purified protein efficiently.
MeSH Terms
Bacterial Proteins
Base Sequence
Carrier Proteins/isolation & purification,metabolism
Cell Cycle/genetics
Cell Nucleus/physiology
DNA Polymerase I/genetics
DNA Replication
Deoxyribonuclease I
Deoxyribonucleases, Type II Site-Specific
Fungal Proteins/genetics
Genes, Fungal
Molecular Sequence Data
Oligonucleotide Probes
Restriction Mapping
Saccharomyces cerevisiae/cytology,genetics,metabolism
Transcription, Genetic
Chemicals
Bacterial Proteins
Carrier Proteins
Fungal Proteins
Oligonucleotide Probes
DNA Polymerase I
endodeoxyribonuclease MluI
Deoxyribonuclease I
Deoxyribonucleases, Type II Site-Specific
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Verma R
Braun Laboratories, California Institute of Technology, Pasaden 91125.
Patapoutian A
Gordon C B
Campbell J L
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