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Roles of uracil-DNA glycosylase and dUTPase in virus replication
被引:109
|作者:
Chen, RX
Wang, HT
Mansky, LM
机构:
[1] Ohio State Univ, Med Ctr, Ctr Retrovirus Res, Dept Mol Virol Immunol & Med Genet, Columbus, OH 43210 USA
[2] Ohio State Univ, Med Ctr, Ctr Comprehens Canc, Columbus, OH 43210 USA
[3] Ohio State Univ, Ohio State Univ Biochem Grad Program, Columbus, OH 43210 USA
[4] Ohio State Univ, Mol Cellular & Dev Biol Grad Program, Columbus, OH 43210 USA
来源:
关键词:
D O I:
10.1099/0022-1317-83-10-2339
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
Herpesviruses and poxviruses are known to encode the DNA repair enzyme uracil-DNA glycosylase (UNG), an enzyme involved in the base excision repair pathway that specifically removes the RNA base uracil from DNA, while at least one retrovirus (human immunodeficiency virus type 1) packages cellular UNG into virus particles. In these instances, UNG is implicated as being important in virus replication. However, a clear understanding of the role(s) of UNG in virus replication remains elusive. Herpesviruses, poxviruses and some retroviruses encode dUTPase, an enzyme that can minimize the misincorporation of uracil into DNA. The encoding of dUTPase by these viruses also implies their importance in virus replication. An understanding at the molecular level of how these viruses replicate in non-dividing cells should provide clues to the biological relevance of UNG and dUTPase function in virus replication.
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页码:2339 / 2345
页数:7
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