Role of mutations identified in ORFs M56 (terminase), M70 (primase) and M98 (endonuclease) in the temperature-sensitive phenotype of murine cytomegalovirus mutant tsm5

被引:3
作者
Timoshenko, Olga [1 ]
Al-Ali, Abdulaziz [1 ]
Martin, Brian A. B. [2 ]
Sweet, Clive [1 ]
机构
[1] Univ Birmingham, Sch Biosci, Birmingham B15 2TT, W Midlands, England
[2] Univ Birmingham, Sch Med, Dept Infect & Immun, Birmingham B15 2TT, W Midlands, England
基金
英国生物技术与生命科学研究理事会;
关键词
Primase; Terminase; Endonuclease; M70; M56; M98; Murine cytomegalovirus; Temperature-sensitive mutant; Attenuated; tsm5; VIRUS; NUCLEASE; PRODUCT; PROTEIN; GENES; CELLS; MOTIF;
D O I
10.1016/j.virol.2009.06.049
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Twenty-six non-synonymous and synonymous mutations have been identified in the temperature-sensitive (B) Mutant (tsm5) of the K181 (Birmingham) variant of routine cytomegalovirus that is deficient in DNA synthesis, processing and packaging at the non-permissive temperature and produces undetectable levels of infectious Virus in mice. Non-synonymous mutations identified in the M70 (primase), M56 (terminase) and M98 (nuclease) ORFs were introduced individually and in combination into the K181 (Perth) variant using BAC technology to examine their role in the ts phenotype. The M56 (G439R) and M98 (P324S) mutations had no evident role in the ts phenotype. However, the C890Y M70 mutation alone and in combination with the M56 and/or M98 mutations tendered the virus ts, unable to replicate in mice and highly defective in DNA synthesis. Reversion of the tyrosine mutation to cysteine or introduction of C890M (experimentally) or C890S (naturally) restored the wt phenotype. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:114 / 122
页数:9
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