Mutations in the Exo III motif of the herpes simplex virus DNA polymerase gene can confer altered drug sensitivities

被引:23
作者
Hwang, YT [1 ]
Smith, JF [1 ]
Gao, L [1 ]
Hwang, CBC [1 ]
机构
[1] SUNY Hlth Sci Ctr, Coll Med, Dept Microbiol & Immunol, Syracuse, NY 13210 USA
关键词
D O I
10.1006/viro.1998.9201
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Two herpes simplex virus mutants containing mutated residues within the conserved fro III motif of the polymerase gene were previously shown to be defective in 3'-5' exonuclease activity and exhibited extremely high mutation frequencies. In this study, we have shown that these mutants also exhibited higher resistance to phosphonoacetic acid and sensitivity to aphidicolin and all nucleoside analogs tested, including acyclovir and gancicolvir, compared to wild-type virus. Marker transfer experiments and sequencing analyses demonstrated that these altered phenotypes were the result of mutations within the fro III motif. The data indicate that, aside from leading to exonuclease deficiency,mutations in the fro III motif may also affect interaction of nucleoside triphosphates with the catalytic sites of polymerase activity, (C) 1998 Academic Press.
引用
收藏
页码:298 / 305
页数:8
相关论文
共 35 条
[31]   SITE-DIRECTED MUTAGENESIS AT THE EXO-III MOTIF OF PHI-29 DNA-POLYMERASE - OVERLAPPING STRUCTURAL DOMAINS FOR THE 3'-5' EXONUCLEASE AND STRAND-DISPLACEMENT ACTIVITIES [J].
SOENGAS, MS ;
ESTEBAN, JA ;
LAZARO, JM ;
BERNAD, A ;
BLASCO, MA ;
SALAS, M ;
BLANCO, L .
EMBO JOURNAL, 1992, 11 (11) :4227-4237
[32]   [DEOXYCYTIDINE-I-125] USED IN A RAPID, SENSITIVE, AND SPECIFIC ASSAY FOR HERPES-SIMPLEX VIRUS TYPE-1 THYMIDINE KINASE [J].
SUMMERS, WC ;
SUMMERS, WP .
JOURNAL OF VIROLOGY, 1977, 24 (01) :314-318
[33]   USE OF SUPPRESSOR ANALYSIS TO IDENTIFY DNA-POLYMERASE MUTATIONS IN HERPES-SIMPLEX VIRUS WHICH AFFECT DEOXYNUCLEOSIDE TRIPHOSPHATE SUBSTRATE-SPECIFICITY [J].
WANG, Y ;
WOODWARD, S ;
HALL, JD .
JOURNAL OF VIROLOGY, 1992, 66 (03) :1814-1816
[34]  
WEISSHART K, 1994, J BIOL CHEM, V269, P22788
[35]   PRIMARY STRUCTURE OF THE CATALYTIC SUBUNIT OF CALF THYMUS DNA POLYMERASE-DELTA - SEQUENCE SIMILARITIES WITH OTHER DNA-POLYMERASES [J].
ZHANG, J ;
CHUNG, DW ;
TAN, CK ;
DOWNEY, KM ;
DAVIE, EW ;
SO, AG .
BIOCHEMISTRY, 1991, 30 (51) :11742-11750