TY - JOUR. T1 - A mammalian bromodomain protein, Brd4, interacts with replication factor C and inhibits progression to S phase. AU - Maruyama, Tetsuo. AU - Farina, Andrea. AU - Dey, Anup. AU - Cheong, JaeHun. AU - Bermudez, Vladimir P.. AU - Tamura, Tomohiko. AU - Sciortino, Selvaggia. AU - Shuman, Jon. AU - Hurwitz, Jerard. AU - Ozato, Keiko. PY - 2002/9. Y1 - 2002/9. N2 - Brd4 belongs to the BET family of nuclear proteins that carry two bromodomains implicated in the interaction with chromatin. Expression of Brd4 correlates with cell growth and is induced during early G1 upon mitogenic stimuli. In the present study, we investigated the role of Brd4 in cell growth regulation. We found that ectopic expression of Brd4 in NIH 3T3 and HeLa cells inhibits cell cycle progression from G1 to S. Coimmunoprecipitation experiments showed that endogenous and transfected Brd4 interacts with replication factor C (RFC), the conserved five-subunit complex essential for DNA replication. In vitro analysis showed ...

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Chromosome cohesion factor involved in sister chromatid cohesion and fidelity of chromosome transmission. Component of one of the cell nuclear antigen loader complexes, CTF18-replication factor C (CTF18-RFC), which consists of CTF18, CTF8, DCC1, RFC2, RFC3, RFC4 and RFC5. The CTF18-RFC complex binds to single-stranded and primed DNAs and has weak ATPase activity that is stimulated by the presence of primed DNA, replication protein A (RPA) and by proliferating cell nuclear antigen (PCNA). The CTF18-RFC complex catalyzes the ATP-dependent loading of PCNA onto primed and gapped DNA. It also interacts with and stimulates DNA polymerase POLH ...

Complete information for RFC5 gene (Protein Coding), Replication Factor C Subunit 5, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

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The identification and purification of human cell proteins required for the production of form I DNA following DNA replication from the simian virus 40 (SV40) origin is described. Using these proteins, complete SV40 DNA replication was reconstituted with only purified DNA replication factors: SV40 large tumor antigen (TAg), replication protein A (RPA), DNA topoisomerases I and II, DNA polymerase alpha-primase, replication factor C (RFC), the proliferating cell nuclear antigen (PCNA), DNA polymerase delta, maturation factor 1 (MF1), and DNA ligase I. MF1, a 5 to 3 exonuclease and DNA ligase I were both identified as essential components for production of covalently closed circular relaxed (form I) DNA. MF1 is probably the same exonuclease previously shown by others to function during DNA synthesis on artificial DNA templates or in conjunction with DNA polymerase alpha from the SV40 origin. Combined with these previous studies, our results suggest that MF1 functions to remove an RNA primer ...

Processivity is an essential feature of DNA replication. D. Jeruzalmi (New York) described loading of the β processivity clamp onto circular DNA in E. coli, which is accomplished by the clamp loader complex, composed of γ, δ, δ′, χ and ψ subunits. The major function of the AAA ATPase in the clamp loader complex is to partially dissociate a stable β dimer. γ and δ′ are both AAA proteins, but only γ is an active ATPase. Upon binding of ATP to γ, changes within the complex cause δ to bind β, a bi‐lobed dimer, and pry it partially open. DNA slips into the open dimer and, upon ATP hydrolysis, the complex dissociates and β closes, thus encircling the DNA.. The major features of bacterial DNA replication are recapitulated in mammals. In eukaryotes, DNA polymerase is stabilized on the DNA by an accessory sliding clamp, PCNA (proliferating cell nuclear antigen). PCNA is loaded on the DNA by a clamp loader, RFC (replication factor C). RFC is a pentameric ring structure consisting of ...

Plays a role as mediator of transcriptional gene silencing (TGS), DNA replication, DNA repair, hypersensitive response (HR) and telomere length regulation. Is required in meiosis for DNA double-strand break (DSB) repair during meiotic homologous recombination. May participate in the RAD51-mediated recombination intermediate repair process. Is important for lagging strand synthesis. Promotes meiotic recombination via a specific pathway for crossovers (COs) that involves the formation of double Holliday Junction (dHJ) intermediates.

Cellular replication factors colocalize with the HPV 18 E1 in HeLa cells.Cells were transfected and analyzed as described previously. Co-immunostaining of HPV18

1] Sequence analysis of a 30 kb DNA segment from yeast chromosome XIV carrying a ribosomal protein gene cluster, the genes encoding a plasma membrane protein and a subunit of replication factor C, and a novel putative serine/threonine protein kinase gene. Maurer K.C.T.et.al. 8553702 ...

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A number of proteins have been isolated from human cells on the basis of their ability to support DNA replication in vitro of the simian virus 40 (SV40) origin of DNA replication. One such protein, replication factor C (RFC), functions with the proliferating cell nuclear antigen (PCNA), replication protein A (RPA), and DNA polymerase delta to synthesize the leading strand at a replication fork. To determine whether these proteins perform similar roles during replication of DNA from origins in cellular chromosomes, we have begun to characterize functionally homologous proteins from the yeast Saccharomyces cerevisiae. RFC from S. cerevisiae was purified by its ability to stimulate yeast DNA polymerase delta on a primed single-stranded DNA template in the presence of yeast PCNA and RPA. Like its human-cell counterpart, RFC from S. cerevisiae (scRFC) has an associated DNA-activated ATPase activity as well as a primer-template, structure-specific DNA binding activity. By analogy with the phage T4 and ...

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1JQL: Mechanism of processivity clamp opening by the delta subunit wrench of the clamp loader complex of E. coli DNA polymerase III.

For cells to proliferate, the genome must be replicated exactly once per cell cycle in a timely and accurate manner. Making this task difficult are multiple other genomic processes, such as transcription and DNA repair, that are concurrently operating on the same genomic template. Replication initiates at specific loci called replication origins that must undergo a series of protein loadings before they can begin to replicate. Although this loading schedule takes place at all origins, individual origins fire at distinct and conserved times during S-phase. It has been suggested that origin firing schedules are defined by their propensity to attract rate limiting replication factors from limited pools (where origins with higher propensities replicate earlier and origins with lower propensities replicate later). This model has not been validated and, furthermore, the factors determining an origins propensity to attract replication factors remains poorly understood. In higher eukaryotes, ...

This gene is a member of the cullin family. The encoded protein forms a complex that functions as an E3 ubiquitin ligase and catalyzes the polyubiquitination of specific protein substrates in the cell. The protein interacts with a ring finger protein, and is required for the proteolysis of several regulators of DNA replication including chromatin licensing and DNA replication factor 1 and cyclin E. Multiple transcript variants encoding different isoforms have been found for this gene ...

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fig 3 conservation of glutamate switch in AAA+ proteins. (a) Sequence alignments of selected members of each clade for which the crystal structures are known. The color scheme follows that used in Figure 4. RFCs, replication factor C small subunit from Archaeoglobus fulgidus; Orc1, Orc1 protein from Aeropyrum pernix; p97D1, p97 D1 AAA+ domain from Mus musculus; SV40, SV40 large T antigen; PspF, PspF from Escherichia coli; HslU, HslU from E. coli; RuvBL1, RuvB-like 1 (TIP49a, Pontin) from Homo sapiens. (b) Plot of side chain torsion angles for 50 active site glutamate (DExx box) residues from AAA+ protein structures in the Protein Data Bank (http://www.rcsb.org/) with a resolution better than 3.5 Å. Only one copy from the asymmetric unit was used if angles were similar, to reduce redundancy. The appropriate glutamate residue was selected from individual PDB files and the side chain torsion angles were calculated using the CCP4 program ANGLES40, then normalized to 0-360° for display. The values ...

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2gcj: The structure of the yFACT Pob3-M domain, its interaction with the DNA replication factor RPA, and a potential role in nucleosome deposition.

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Feng, X., Noguchi, Y., Barbon, M., Stillman, B., Speck, C., Li, H. (2021). The structure of ORC-Cdc6 on an origin DNA reveals the mechanism of ORC activation by the replication initiator Cdc6. Nature Communications 12, 3883 ...

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