Two functional domains of the ε subunit of DNA polymerase III

被引:40
作者
Perrino, FW [1 ]
Harvey, S [1 ]
McNeill, SM [1 ]
机构
[1] Wake Forest Univ, Bowman Gray Sch Med, Dept Biochem, Winston Salem, NC 27157 USA
关键词
D O I
10.1021/bi991429+
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The epsilon subunit is the 3' --> 5' proofreading exonuclease that associates with the alpha and theta subunits in the E. coli DNA polymerase III. Two fragments of the epsilon protein were prepared, and binding of these epsilon fragments with alpha and theta was investigated using gel filtration chromatography and exonuclease stimulation assays. The N-terminal fragment of epsilon, containing amino acids 2-186 (epsilon 186), is a relatively protease-resistant core domain of the exonuclease. The purified recombinant epsilon 186 protein catalyzes the cleavage of 3' terminal nucleotides, demonstrating that the exonuclease domain of epsilon is present in the N-terminal region of the protein. The absence of the C-terminal 57 amino acids of epsilon in the epsilon 186 protein reduces the binding affinity of epsilon 186 for alpha by at least 400-fold relative to the binding affinity of epsilon for alpha. In addition, stimulation of the epsilon 186 exonuclease by alpha using a partial duplex DNA is about 50-fold lower than stimulation of the epsilon exonuclease by alpha. These results indicate that the C-terminal region of epsilon is required in the epsilon alpha association. To directly demonstrate that the C-terminal region of epsilon contains the alpha-association domain fusion protein, constructs containing the maltose-binding protein (MBP) and fragments of the C-terminal region of epsilon were prepared. Gel filtration analysis demonstrates that the alpha-association domain of epsilon is contained within the C-terminal 40 amino acids of epsilon. Also, the epsilon 186 protein forms a tight complex with theta, demonstrating that the association of theta with epsilon is localized to the N-terminal region of epsilon. Association of epsilon 186 and theta is further supported by the stimulation of the epsilon 186 exonuclease in the presence of theta. These data support the concept that epsilon contains a catalytic domain located within the N-terminal region and an alpha-association domain located within the C-terminal region of the protein.
引用
收藏
页码:16001 / 16009
页数:9
相关论文
共 48 条
[21]   Effects of mutations on the partitioning of DNA substrates between the polymerase and 3′-5′ exonuclease sites of DNA polymerase I (Klenow fragment) [J].
Lam, WC ;
Van der Schans, EJC ;
Joyce, CM ;
Millar, DP .
BIOCHEMISTRY, 1998, 37 (06) :1513-1522
[22]   ISOLATION AND CHARACTERIZATION OF MUTANTS WITH DELETIONS IN DNAQ, THE GENE FOR THE EDITING SUBUNIT OF DNA POLYMERASE-III IN SALMONELLA-TYPHIMURIUM [J].
LANCY, ED ;
LIFSICS, MR ;
KEHRES, DG ;
MAURER, R .
JOURNAL OF BACTERIOLOGY, 1989, 171 (10) :5572-5580
[23]   DNA-REPLICATION DEFECT IN SALMONELLA-TYPHIMURIUM MUTANTS LACKING THE EDITING (EPSILON SUBUNIT OF DNA POLYMERASE-III [J].
LIFSICS, MR ;
LANCY, ED ;
MAURER, R .
JOURNAL OF BACTERIOLOGY, 1992, 174 (21) :6965-6973
[24]   PROOFREADING BY DNA POLYMERASE-III OF ESCHERICHIA-COLI DEPENDS ON COOPERATIVE INTERACTION OF THE POLYMERASE AND EXONUCLEASE SUBUNITS [J].
MAKI, H ;
KORNBERG, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (13) :4389-4392
[25]  
MAKI H, 1985, J BIOL CHEM, V260, P2987
[26]  
MCHENRY CS, 1991, J BIOL CHEM, V266, P19127
[27]  
MCHENRY CS, 1979, J BIOL CHEM, V254, P1748
[28]   Kinetic mechanism of the 3'->5' proofreading exonuclease of DNA polymerase .3. Analysis by steady state and pre-steady state methods [J].
Miller, H ;
Perrino, FW .
BIOCHEMISTRY, 1996, 35 (39) :12919-12925
[29]   THE ESCHERICHIA-COLI GALK2 PAPILLATION ASSAY - ITS SPECIFICITY AND APPLICATION TO 7 NEWLY ISOLATED MUTATOR STRAINS [J].
OLLER, AR ;
FIJALKOWSKA, IJ ;
SCHAAPER, RM .
MUTATION RESEARCH, 1993, 292 (02) :175-185
[30]   STRUCTURE OF LARGE FRAGMENT OF ESCHERICHIA-COLI DNA-POLYMERASE-I COMPLEXED WITH DTMP [J].
OLLIS, DL ;
BRICK, P ;
HAMLIN, R ;
XUONG, NG ;
STEITZ, TA .
NATURE, 1985, 313 (6005) :762-766