Reconstitution of recombinant human replication factor C (RFC) and identification of an RFC subcomplex possessing DNA-dependent ATPase activity

Ellison, V., Stillman, B. (March 1998) Reconstitution of recombinant human replication factor C (RFC) and identification of an RFC subcomplex possessing DNA-dependent ATPase activity. Journal of Biological Chemistry, 273 (10). pp. 5979-87. ISSN 0021-9258

[thumbnail of Paper]
Preview
PDF (Paper)
Reconstitution of Recombinant Human Replication Factor C.pdf - Published Version

Download (387kB) | Preview
URL: http://www.ncbi.nlm.nih.gov/pubmed/9488738
DOI: 10.1074/jbc.273.10.5979

Abstract

Replication factor C (RFC) is a five-subunit protein complex required for coordinate leading and lagging strand DNA synthesis during S phase and DNA repair in eukaryotic cells. It functions to load the proliferating cell nuclear antigen (PCNA), a processivity factor for polymerases delta and epsilon, onto primed DNA templates. This process, which is ATP-dependent, is carried out by 1) recognition of the primer terminus by RFC () binding to and disruption of the PCNA trimer, and then 3) topologically linking the PCNA to the DNA. In this report, we describe the purification and properties of recombinant human RFC expressed in Sf9 cells from baculovirus expression vectors. Like native RFC derived from 293 cells, recombinant RFC was found to support SV40 DNA synthesis and polymerase delta DNA synthesis in vitro and to possess an ATPase activity that was highly stimulated by DNA and further augmented by PCNA. Assembly of RFC was observed to involve distinct subunit interactions in which both the 36- and 38-kDa subunits interacted with the 37-kDa subunit, and the 40-kDa subunit interacted with the 36-kDa subunit-37-kDa subunit subcomplex. The 140-kDa subunit was found to require interactions primarily with the 38- and 40-kDa subunits for incorporation into the complex. In addition, a stable subcomplex lacking the 140-kDa subunit, although defective for DNA replication, was found to possess DNA-dependent ATPase activity that was not responsive to the addition of PCNA.

Item Type: Paper
Uncontrolled Keywords: Adenosinetriphosphatase analysis chemistry metabolism Animals Baculoviridae genetics DNA Helicases DNA Replication genetics DNA-Binding Proteins chemistry genetics Gene Expression genetics Homeodomain Proteins Humans Precipitin Tests Proliferating Cell Nuclear Antigen metabolism Proto-Oncogene Proteins c-bcl-2 Proto Oncogene Recombinant Proteins isolation & purification metabolism Replication Factor C Repressor Proteins Saccharomyces cerevisiae Proteins Simian virus 40 genetics Spodoptera genetics
Subjects: bioinformatics > genomics and proteomics > genetics & nucleic acid processing > DNA, RNA structure, function, modification > DNA replication
CSHL Authors:
Communities: CSHL labs > Stillman lab
Highlight: Stillman, Bruce W.
Depositing User: CSHL Librarian
Date: 6 March 1998
Date Deposited: 07 Mar 2012 15:37
Last Modified: 20 Jun 2017 19:29
Related URLs:
URI: https://repository.cshl.edu/id/eprint/24969

Actions (login required)

Administrator's edit/view item Administrator's edit/view item
CSHL HomeAbout CSHLResearchEducationNews & FeaturesCampus & Public EventsCareersGiving