Deletion analysis of the large subunit p140 in human replication factor C reveals regions required for complex formation and replication activities Journal Article


Authors: Uhlmann, F.; Cai, J.; Gibbs, E.; O'Donnell, M.; Hurwitz, J.
Article Title: Deletion analysis of the large subunit p140 in human replication factor C reveals regions required for complex formation and replication activities
Abstract: Replication factor C (RFC) and proliferating cell nuclear antigen (PCNA) are processivity factors for eukaryotic DNA polymerases δ and ε. RFC contains multiple activities, including its ability to recognize and bind to a DNA primer end and load the ring-shaped PCNA onto DNA in an ATP-dependent reaction. PCNA then tethers the polymerase to the template allowing processive DNA chain elongation. Human RFC consists of five distinct subunits (p140, p40, p38, p37, and p36), and RFC activity can be reconstituted from the five cloned gene products. To characterize the role of the large subunit p140 in the function of the RFC complex, deletion mutants were created that defined a region within the p140 C terminus required for complex formation with the four small subunits. Deletion of the p140 N-terminal half, including the DNA ligase homology domain, resulted in the formation of an RFC complex with enhanced activity in replication and PCNA loading. Deletion of additional N-terminal amino acids, including those constituting the RFC homology box II that is conserved among all five RFC subunits, disrupted RFC replication function. DNA primer end recognition and PCNA binding activities, located in the p140 C-terminal half, were unaffected in this mutant, but PCNA loading was abolished.
Keywords: human cell; dna-binding proteins; sequence deletion; dna polymerase; dna replication; protein conformation; complex formation; dna repair; genetic transcription; homeodomain proteins; hela cell; structure-activity relationship; molecular cloning; dna; eukaryota; saccharomyces cerevisiae proteins; adenosine triphosphate; cycline; replication protein c; dna binding; repressor proteins; proto-oncogene proteins c-bcl-2; deletion mutant; proliferating cell nuclear antigen; dna, circular; humans; human; priority journal; article
Journal Title: Journal of Biological Chemistry
Volume: 272
Issue: 15
ISSN: 0021-9258
Publisher: American Society for Biochemistry and Molecular Biology  
Date Published: 1997-04-11
Start Page: 10058
End Page: 10064
Language: English
DOI: 10.1074/jbc.272.15.10058
PUBMED: 9092549
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 17 March 2017 -- Source: Scopus
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  1. Jerard Hurwitz
    206 Hurwitz
  2. Emma Gibbs
    14 Gibbs