Literature DB >> 7118945

The beta subunit of the DNA polymerase III holoenzyme becomes inaccessible to antibody after formation of an initiation complex with primed DNA.

K O Johanson, C S McHenry.   

Abstract

The initiation of the DNA polymerase III holoenzyme-catalyzed reaction is blocked by antibody directed against the beta subunit; elongation is unaffected (Johanson, K., and McHenry, C. (1980) J. Biol. Chem. 255, 10984-10990). We have developed an immunological method for quantitating nanogram quantities of beta in reaction complexes. Using this method, we have demonstrated that beta is present in all stages of the DNA polymerase III holoenzyme reaction. Upon initiation complex formation, the antigenic determinants of beta become inaccessible to anti-beta immunoglobulin G. The methods described herein should be generally applicable to the study of a variety of multienzyme complexes. Even after conversion of a primed G4 single strand to the duplex replicative form, beta does not readily dissociate. This creates a kinetic barrier to the overall holoenzyme replicative reaction.

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Year:  1982        PMID: 7118945

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  16 in total

1.  Molecular cloning, sequencing, and overexpression of the structural gene encoding the delta subunit of Escherichia coli DNA polymerase III holoenzyme.

Authors:  J R Carter; M A Franden; R Aebersold; C S McHenry
Journal:  J Bacteriol       Date:  1992-11       Impact factor: 3.490

2.  Chaperoning of a replicative polymerase onto a newly assembled DNA-bound sliding clamp by the clamp loader.

Authors:  Christopher D Downey; Charles S McHenry
Journal:  Mol Cell       Date:  2010-02-26       Impact factor: 17.970

3.  Polymerase chaperoning and multiple ATPase sites enable the E. coli DNA polymerase III holoenzyme to rapidly form initiation complexes.

Authors:  Christopher D Downey; Elliott Crooke; Charles S McHenry
Journal:  J Mol Biol       Date:  2011-07-28       Impact factor: 5.469

4.  The gamma subunit of DNA polymerase III holoenzyme of Escherichia coli is produced by ribosomal frameshifting.

Authors:  A M Flower; C S McHenry
Journal:  Proc Natl Acad Sci U S A       Date:  1990-05       Impact factor: 11.205

5.  Functional order of assembly of herpes simplex virus DNA replication proteins into prereplicative site structures.

Authors:  L M Liptak; S L Uprichard; D M Knipe
Journal:  J Virol       Date:  1996-03       Impact factor: 5.103

6.  DNA Polymerase α Subunit Residues and Interactions Required for Efficient Initiation Complex Formation Identified by a Genetic Selection.

Authors:  Janet C Lindow; Paul R Dohrmann; Charles S McHenry
Journal:  J Biol Chem       Date:  2015-05-18       Impact factor: 5.157

7.  Interaction of DNA polymerase III gamma and beta subunits in vivo in Salmonella typhimurium.

Authors:  J Engstrom; A Wong; R Maurer
Journal:  Genetics       Date:  1986-07       Impact factor: 4.562

8.  The rate of polymerase release upon filling the gap between Okazaki fragments is inadequate to support cycling during lagging strand synthesis.

Authors:  Paul R Dohrmann; Carol M Manhart; Christopher D Downey; Charles S McHenry
Journal:  J Mol Biol       Date:  2011-10-01       Impact factor: 5.469

9.  Identification, isolation, and characterization of the structural gene encoding the delta' subunit of Escherichia coli DNA polymerase III holoenzyme.

Authors:  J R Carter; M A Franden; R Aebersold; C S McHenry
Journal:  J Bacteriol       Date:  1993-06       Impact factor: 3.490

Review 10.  DNA polymerase III holoenzyme of Escherichia coli: components and function of a true replicative complex.

Authors:  C S McHenry
Journal:  Mol Cell Biochem       Date:  1985-02       Impact factor: 3.396

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