Literature DB >> 1975812

Two forms of DNA polymerase delta from mouse cells. Purification and properties.

M Goulian1, S M Herrmann, J W Sackett, S L Grimm.   

Abstract

A procedure is described for the purification from cultured mouse cells of two DNA polymerase "delta-like" enzymes, as defined by intrinsic 3'-exonuclease activity, inhibition by aphidicolin, and relative insensitivity to N2-(p-n-butylphenyl)-dGTP. One of the two enzymes has been purified to near homogeneity and, similar to the DNA polymerase delta from calf thymus described by Lee et al. (Lee, M. Y. W. T., Tan, C. K., Downey, K. M., and So, A. G. (1984) Biochemistry 23, 1906-1913), it has a total molecular mass of 178 kDa (from sedimentation velocity of 8.0 S and Stokes radius of 54 A) and is composed of one each of 125- and 50-kDa polypeptides. It also resembles the DNA polymerase delta of Lee et al. in being stimulated by proliferating cell nuclear antigen (PCNA). It is the first clear structural and functional counterpart of the calf thymus enzyme. The major difference between the mouse DNA polymerase delta and the calf thymus enzyme of Lee et al. is that, under specific conditions, the mouse enzyme is active with poly(dA).oligo(dT) in the absence of PCNA, whereas the activity of the calf thymus enzyme with this template is reported to be completely dependent on PCNA. The reason for this difference is not known at this time. The second mouse cell enzyme has a molecular mass of 112 kDa (from sedimentation velocity of 6.3 S and Stokes radius of 43.0 A) and consists of a single polypeptide of 123-125 kDa in denaturing gels (p125). On the basis of its apparent formation by dissociation of DNA polymerase delta, and multiple similarities with DNA polymerase delta in enzymatic properties, the p125 is provisionally identified as the 125-kDa polypeptide of DNA polymerase delta. The p125 does not respond to PCNA, suggesting that the 50-kDa polypeptide is required for the stimulation of DNA polymerase delta by PCNA. The presence of the p125 in cell extracts would explain reports that DNA polymerase delta consists of a single polypeptide of approximately 125 kDa and/or thast it has a smaller molecular mass than DNA polymerase delta of Lee et al. and is not affected by PCNA (this does not apply to PCNA-independent DNA polymerase delta-like enzymes with higher molecular mass than the polymerase delta of Lee et al., which have recently been named DNA polymerases epsilon).

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Year:  1990        PMID: 1975812

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


  12 in total

1.  Primary structure of the catalytic subunit of human DNA polymerase delta and chromosomal location of the gene.

Authors:  D W Chung; J A Zhang; C K Tan; E W Davie; A G So; K M Downey
Journal:  Proc Natl Acad Sci U S A       Date:  1991-12-15       Impact factor: 11.205

2.  The p15 carboxyl-terminal proteolysis product of the human immunodeficiency virus type 1 reverse transcriptase p66 has DNA polymerase activity.

Authors:  P Hafkemeyer; E Ferrari; J Brecher; U Hübscher
Journal:  Proc Natl Acad Sci U S A       Date:  1991-06-15       Impact factor: 11.205

3.  DNA polymerases alpha, delta, and epsilon of Novikoff hepatoma cells differ from those of normal rat liver in physicochemical and catalytic properties.

Authors:  O Popanda; G Fox; H W Thielmann
Journal:  J Mol Med (Berl)       Date:  1995-05       Impact factor: 4.599

4.  The fission yeast Cdc1 protein, a homologue of the small subunit of DNA polymerase delta, binds to Pol3 and Cdc27.

Authors:  S A MacNeill; S Moreno; N Reynolds; P Nurse; P A Fantes
Journal:  EMBO J       Date:  1996-09-02       Impact factor: 11.598

5.  Functional interactions of a homolog of proliferating cell nuclear antigen with DNA polymerases in Archaea.

Authors:  I K Cann; S Ishino; I Hayashi; K Komori; H Toh; K Morikawa; Y Ishino
Journal:  J Bacteriol       Date:  1999-11       Impact factor: 3.490

6.  Preferential inhibition of DNA polymerases alpha, delta, and epsilon from Novikoff hepatoma cells by inhibitors of cell proliferation.

Authors:  G Fox; O Popanda; L Edler; H W Thielmann
Journal:  J Cancer Res Clin Oncol       Date:  1996       Impact factor: 4.553

7.  Studies on the interactions between human replication factor C and human proliferating cell nuclear antigen.

Authors:  G Zhang; E Gibbs; Z Kelman; M O'Donnell; J Hurwitz
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-02       Impact factor: 11.205

8.  The N-terminal region of DNA polymerase delta catalytic subunit is necessary for holoenzyme function.

Authors:  S B Schumacher; M Stucki; U Hübscher
Journal:  Nucleic Acids Res       Date:  2000-01-15       Impact factor: 16.971

9.  DNA polymerase delta from embryos of Drosophila melanogaster.

Authors:  C S Chiang; P G Mitsis; I R Lehman
Journal:  Proc Natl Acad Sci U S A       Date:  1993-10-01       Impact factor: 11.205

10.  The small subunit is required for functional interaction of DNA polymerase delta with the proliferating cell nuclear antigen.

Authors:  J Q Zhou; H He; C K Tan; K M Downey; A G So
Journal:  Nucleic Acids Res       Date:  1997-03-15       Impact factor: 16.971

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