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Molecular and Cellular Biology, April 2001, p. 2581-2593, Vol. 21, No. 7
0270-7306/01/$04.00+0 DOI: 10.1128/MCB.21.7.2581-2593.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Two Immunologically Distinct Human DNA
Polymerase
-Primase Subpopulations Are Involved in Cellular
DNA Replication
Silke
Dehde,1
Gabor
Rohaly,1
Oliver
Schub,2
Heinz-Peter
Nasheuer,2
Wolfgang
Bohn,1
Jan
Chemnitz,1
Wolfgang
Deppert,1 and
Irena
Dornreiter*,1
Heinrich-Pette-Institut für
Experimentelle Virologie und Immunologie an der Universität
Hamburg, D-20251 Hamburg,1 and Institut
für Molekulare Biotechnologie, Abteilung Biochemie, D-07745
Jena,2 Germany
Received 31 August 2000/Returned for modification 3 October
2000/Accepted 27 December 2000
Metabolic labeling of primate cells revealed the existence of
phosphorylated and hypophosphorylated DNA polymerase
-primase (Pol-Prim) populations that are distinguishable by monoclonal antibodies. Cell cycle studies showed that the hypophosphorylated form
was found in a complex with PP2A and cyclin E-Cdk2 in G1, whereas the phosphorylated enzyme was associated with a cyclin A kinase
in S and G2. Modification of Pol-Prim by PP2A and Cdks regulated the interaction with the simian virus 40 origin-binding protein large T antigen and thus initiation of DNA replication. Confocal microscopy demonstrated nuclear colocalization of
hypophosphorylated Pol-Prim with MCM2 in S phase nuclei, but its
presence preceded 5-bromo-2'-deoxyuridine (BrdU) incorporation. The
phosphorylated replicase exclusively colocalized with the BrdU signal,
but not with MCM2. Immunoprecipitation experiments proved that only
hypophosphorylated Pol-Prim associated with MCM2. The data indicate
that the hypophosphorylated enzyme initiates DNA replication at
origins, and the phosphorylated form synthesizes the primers for the
lagging strand of the replication fork.
*
Corresponding author. Mailing address:
Heinrich-Pette-Institut für Experimentelle Virologie und
Immunologie, Martinistr. 52, D-20251 Hamburg, Germany. Phone:
40-48051-231. Fax: 40-48051-117. E-mail:
dornreit{at}hpi.uni-hamburg.de.
Molecular and Cellular Biology, April 2001, p. 2581-2593, Vol. 21, No. 7
0270-7306/01/$04.00+0 DOI: 10.1128/MCB.21.7.2581-2593.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
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