Literature DB >> 11056476

The puzzle of PCNA's many partners.

E Warbrick1.   

Abstract

The identification of proteins that interact with proliferating cell nuclear antigen (PCNA) has recently been a rapidly expanding field of discovery. PCNA is involved in many aspects of DNA replication and processing, forming a sliding platform that can mediate the interaction of proteins with DNA. It is striking that many proteins bind to PCNA through a small region containing a conserved motif; these include proteins involved in cell cycle regulation as well as those involved in DNA processing. Sequential and regulated binding of motif-containing proteins to PCNA may contribute to the ordering of events during DNA replication and repair. Results from bacteriophages and archaea show that the structural basis for the interaction of this motif with PCNA is extremely ancient. The analysis of how such functional motifs have been recruited to proteins in present day organisms helps us to understand how these complex systems arose from ancestral organisms.

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Year:  2000        PMID: 11056476     DOI: 10.1002/1521-1878(200011)22:11<997::AID-BIES6>3.0.CO;2-#

Source DB:  PubMed          Journal:  Bioessays        ISSN: 0265-9247            Impact factor:   4.345


  165 in total

1.  Posttranslational modification of the umuD-encoded subunit of Escherichia coli DNA polymerase V regulates its interactions with the beta processivity clamp.

Authors:  Mark D Sutton; Issay Narumi; Graham C Walker
Journal:  Proc Natl Acad Sci U S A       Date:  2002-04-16       Impact factor: 11.205

2.  On the specificity of interaction between the Saccharomyces cerevisiae clamp loader replication factor C and primed DNA templates during DNA replication.

Authors:  Manju M Hingorani; Maria Magdalena Coman
Journal:  J Biol Chem       Date:  2002-10-04       Impact factor: 5.157

3.  Molecular characterization of mouse gastric epithelial progenitor cells.

Authors:  Jason C Mills; Niklas Andersson; Chieu V Hong; Thaddeus S Stappenbeck; Jeffrey I Gordon
Journal:  Proc Natl Acad Sci U S A       Date:  2002-10-30       Impact factor: 11.205

4.  Crystal structures of two active proliferating cell nuclear antigens (PCNAs) encoded by Thermococcus kodakaraensis.

Authors:  Jane E Ladner; Miao Pan; Jerard Hurwitz; Zvi Kelman
Journal:  Proc Natl Acad Sci U S A       Date:  2011-01-26       Impact factor: 11.205

5.  A peptide switch regulates DNA polymerase processivity.

Authors:  Francisco J López de Saro; Roxana E Georgescu; Mike O'Donnell
Journal:  Proc Natl Acad Sci U S A       Date:  2003-11-20       Impact factor: 11.205

6.  Competitive processivity-clamp usage by DNA polymerases during DNA replication and repair.

Authors:  Francisco J López de Saro; Roxana E Georgescu; Myron F Goodman; Mike O'Donnell
Journal:  EMBO J       Date:  2003-12-01       Impact factor: 11.598

7.  Nuclear factories for signalling and repairing DNA double strand breaks in living fission yeast.

Authors:  Peter Meister; Mickaël Poidevin; Stefania Francesconi; Isabelle Tratner; Patrick Zarzov; Giuseppe Baldacci
Journal:  Nucleic Acids Res       Date:  2003-09-01       Impact factor: 16.971

8.  Intermolecular ion pairs maintain the toroidal structure of Pyrococcus furiosus PCNA.

Authors:  Shigeki Matsumiya; Sonoko Ishino; Yoshizumi Ishino; Kosuke Morikawa
Journal:  Protein Sci       Date:  2003-04       Impact factor: 6.725

9.  Inflammatory biomarkers of sulfur mustard analog 2-chloroethyl ethyl sulfide-induced skin injury in SKH-1 hairless mice.

Authors:  Neera Tewari-Singh; Sumeet Rana; Mallikarjuna Gu; Arttatrana Pal; David J Orlicky; Carl W White; Rajesh Agarwal
Journal:  Toxicol Sci       Date:  2008-12-15       Impact factor: 4.849

10.  The amino terminus of the Saccharomyces cerevisiae DNA helicase Rrm3p modulates protein function altering replication and checkpoint activity.

Authors:  Jessica B Bessler; Virginia A Zakian
Journal:  Genetics       Date:  2004-11       Impact factor: 4.562

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