The origin recognition complex in silencing, cell cycle progression, and DNA replication.
This report describes the isolation of ORC5, the gene encoding the fifth largest subunit of the origin recognition complex, and the properties of mutants with a defective allele of ORC5. The orc5-1 mutation caused temperature-sensitive growth and, at the restrictive temperature, caused cell cycle arrest. At the permissive temperature, the ... orc5-1 mutation caused an elevated plasmid loss rate that could be suppressed by additional tandem origins of DNA replication. The sequence of ORC5 revealed a potential ATP binding site, making Orc5p a candidate for a subunit that mediates the ATP-dependent binding of ORC to origins. Genetic interactions among orc2-1 and orc5-1 and other cell cycle genes provided further evidence for a role for the origin recognition complex (ORC) in DNA replication. The silencing defect caused by orc5-1 strengthened previous connections between ORC and silencing, and combined with the phenotypes caused by orc2 mutations, suggested that the complex itself functions in both processes.
Mesh Terms:
Amino Acid Sequence, Base Sequence, Cell Cycle, Cell Cycle Proteins, Cloning, Molecular, Crosses, Genetic, DNA Replication, DNA, Fungal, DNA-Binding Proteins, Genes, Fungal, Molecular Sequence Data, Mutation, Origin Recognition Complex, Phenotype, Plasmids, Polymerase Chain Reaction, Repressor Proteins, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins, Temperature, Time Factors, Transcription, Genetic
Amino Acid Sequence, Base Sequence, Cell Cycle, Cell Cycle Proteins, Cloning, Molecular, Crosses, Genetic, DNA Replication, DNA, Fungal, DNA-Binding Proteins, Genes, Fungal, Molecular Sequence Data, Mutation, Origin Recognition Complex, Phenotype, Plasmids, Polymerase Chain Reaction, Repressor Proteins, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins, Temperature, Time Factors, Transcription, Genetic
Mol. Biol. Cell
Date: Jun. 01, 1995
PubMed ID: 7579692
View in: Pubmed Google Scholar
Download Curated Data For This Publication
14622
Switch View:
- Interactions 12