Identification of conserved residues contributing to the activities of adenovirus DNA polymerase

被引:23
作者
Liu, HT [1 ]
Naismith, JH [1 ]
Hay, RT [1 ]
机构
[1] Univ St Andrews, Ctr Biomol Sci, St Andrews KY16 9ST, Fife, Scotland
基金
英国惠康基金;
关键词
D O I
10.1128/JVI.74.24.11681-11689.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Adenovirus codes for a DNA polymerase that is a member of the DNA polymerase a family and uses a protein primer for initiation of DNA synthesis. It contains motifs characteristic of a proofreading 3 ' -5 ' -exonuclease domain located in the N-terminal region and several polymerase motifs located in the C-terminal region. To determine the role of adenovirus DNA polymerase in DNA replication, 22 site-directed mutations were introduced into the conserved DNA polymerase motifs in the C-terminal region of adenovirus DNA polymerase and the mutant forms were expressed in insect cells using a baculovirus expression system. Each mutant enzyme was tested for DNA binding activity, the ability to interact with pTP, DNA polymerase catalytic activity, and the ability to participate in the initiation of adenovirus DNA replication. The mutant phenotypes identify functional domains within the adenovirus DNA polymerase and allow discrimination between the roles of conserved residues in the various activities carried out by the protein. Using the functional data in this study and the previously published structure of the bacteriophage RB69 DNA polymerase (J. Wang et al., Cell 89:1087-1099, 1997), it is possible to envisage how the conserved domains in the adenovirus DNA polymerase function.
引用
收藏
页码:11681 / 11689
页数:9
相关论文
共 68 条
[1]   STRUCTURES OF DNA AND RNA-POLYMERASES AND THEIR INTERACTIONS WITH NUCLEIC-ACID SUBSTRATES [J].
ARNOLD, E ;
DING, JP ;
HUGHES, SH ;
HOSTOMSKY, Z .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 1995, 5 (01) :27-38
[2]   STRUCTURAL AND FUNCTIONAL-RELATIONSHIPS BETWEEN PROKARYOTIC AND EUKARYOTIC DNA-POLYMERASES [J].
BERNAD, A ;
ZABALLOS, A ;
SALAS, M ;
BLANCO, L .
EMBO JOURNAL, 1987, 6 (13) :4219-4225
[3]   A CONSERVED 3'-]5' EXONUCLEASE ACTIVE-SITE IN PROKARYOTIC AND EUKARYOTIC DNA-POLYMERASES [J].
BERNAD, A ;
BLANCO, L ;
LAZARO, JM ;
MARTIN, G ;
SALAS, M .
CELL, 1989, 59 (01) :219-228
[4]  
BLASCO MA, 1993, J BIOL CHEM, V268, P16763
[5]  
BLASCO MA, 1993, J BIOL CHEM, V268, P24106
[6]   COMPILATION, ALIGNMENT, AND PHYLOGENETIC-RELATIONSHIPS OF DNA-POLYMERASES [J].
BRAITHWAITE, DK ;
ITO, J .
NUCLEIC ACIDS RESEARCH, 1993, 21 (04) :787-802
[7]   An improved PCR-based method for site directed mutagenesis using megaprimers [J].
Brons-Poulsen, J ;
Petersen, NE ;
Horder, M ;
Kristiansen, K .
MOLECULAR AND CELLULAR PROBES, 1998, 12 (06) :345-348
[8]   DISSECTION OF FUNCTIONAL DOMAINS OF ADENOVIRUS DNA-POLYMERASE BY LINKER-INSERTION MUTAGENESIS [J].
CHEN, M ;
HORWITZ, MS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (16) :6116-6120
[9]  
COPELAND WC, 1993, J BIOL CHEM, V268, P11041
[10]  
COPELAND WC, 1993, J BIOL CHEM, V268, P11028