The origin recognition complex (ORC), a multisubunit protein identified in Saccharomyces cerevisiae, binds to chromosomal replicators and is required for the initiation of cellular DNA replication. Complementary DNAs (cDNAs) encoding proteins related to the two largest subunits of ORC were cloned from various eukaryotes. The cDNAs encoding proteins related to S. cerevisiae Orc1p were cloned from the budding yeast Kluyveromyces lactis, the fission yeast Schizosaccharomyces pombe, and human cells. These proteins show similarity to regulators of the S and M phases of the cell cycle. Genetic analysis of orc1+ from S. pombe reveals that it is essential for cell viability. The cDNAs encoding proteins related to S. cerevisiae Orc2p were cloned from Arabidopsis thaliana, Caenorhabditis elegans, and human cells. The human ORC-related proteins interact in vivo to form a complex. These studies studies suggest that ORC subunits are conserved and that the role of ORC is a general feature of eukaryotic DNA replication.

The location of origins of DNA replication within the Saccharomyces cerevisiae genome is primarily determined by the origin recognition complex (ORC) interacting with specific DNA sequences. The analogous situation in vertebrate cells is far less clear, although ORC subunits have been identified in several vertebrate organisms including Xenopus laevis. Monoclonal antibodies were raised against Xenopus Orc1p and used for single-step immunoaffinity purification of the entire ORC from an egg extract. Six polypeptides (ϳ110, 68, 64, 48, 43, and 27 kDa) copurified with Xenopus Orc1p. Protein sequencing also showed the 64-kDa protein to be the previously identified Xenopus Orc2p. Microsequencing of the 43-and 48-kDa proteins that copurified with Orc1p and Orc2p led to their identification as the Orc4p and Orc5p subunits, respectively. Peptide sequences from the 43-kDa protein also allowed the isolation of cDNAs encoding the Xenopus, mouse, and human ORC4 subunits. Human ORC5 was also cloned; its sequence displayed extensive homology to both Drosophila and yeast ORC5. Surprisingly, comparison of the amino acid sequences of Orc1p, Orc4p, and Orc5p suggests that they are structurally related to each other and to the replication initiation protein, Cdc6p. Finally, we present the sequence of the putative Xenopus and human Orc3p.The initiation of DNA replication in eukaryotes is tightly regulated such that all the DNA is replicated precisely once per cell cycle from a number of discrete replication origins (Refs. 1-3; for reviews, see Refs. 4 and 5). The nature of this regulation, however, is not well understood as only a small fraction of proteins involved in this process have been identified. Moreover, with the exception of budding yeast, the DNA sequences that define the origin of DNA replication on chromosomes remain an almost complete mystery in higher eukaryotes.Present knowledge of the control over initiation of DNA replication in an eukaryotic cell is largely based on experiments done in the yeast Saccharomyces cerevisiae. In this yeast, DNA replication starts from well defined origins, known as the autonomously replicating sequences (6). An essential, bipartite DNA sequence in all S. cerevisiae replication origins is recognized by the six-subunit origin recognition complex (ORC), 1 which is itself essential for initiation of DNA replication (7-20). The ORC also functions in the control of gene silencing, a function that is, at least partially, separable from the functions in initiation of DNA replication (9, 10, 15, 21-23). Proteins homologous to individual subunits of the S. cerevisiae ORC have been identified recently in other yeast species and from animal and plant cells. Orc1p and Orc2p were found in Schizosaccharomyces pombe, Drosophila, Xenopus, and humans, and Orc5p has been identified in Drosophila (24 -30). More recently, the human Orc4p has been identified and shown to co-immunoprecipitate with human Orc2p (31). Immunodepletion of ORC inhibited initiation of DNA replication in a Xenopus egg extract, sugge...